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<html>
<head><title>The transparency of life: Cataracts as a model of age-related disease</title></head>
<body>
<h1>
The transparency of life: Cataracts as a model of age-related disease
</h1>
<em><p>
Cataracts can disappear when the eye's metabolic condition is corrected. A supply of energy is essential
to maintain the transparent structure.
</p>
<p>
Lactic acid increases as carbon dioxide decreases, during a typical energy deficiency. Deficient
thyroid, and the resulting excess of cortisol relative to pregnenolone and progesterone, define the
energy deficiency.
</p>
<p>
Increased lactate relative to CO2 in the cell alters cell pH and electrical charge, causing swelling.
Swelling and increased water content characterize the cataract.
</p>
<p>
High altitude is inversely related to cataracts, despite the known role of sunlight in causing
cataracts; this is a strong confirmation of the protective role of carbon dioxide.
</p></em>
<hr />
<p>
In the markets around Lake Patzcuaro, they sell green transparent fish, about 6 inches long. When cooked,
the meat is white, like ordinary fish. Most fish filets are a little translucent, but are at least cloudy,
and usually pink by transmitted light. I don"t know how the transparent fish work, because it seems that the
blood and the network of blood vessels needed to sustain muscle activity would diffuse the light. Anyway,
cooking disrupts the mysteriously ordered state of water and proteins that makes them transparent, roughly
the way egg-white loses its transparency when it is cooked. I have never heard a convincing explanation for
the opacity of cooked egg-white, either, but anything that disrupts the original structuring of the
protein-water interaction will destroy the transparency.
</p>
<p>
Around 1970, I used a technique called nuclear magnetic resonance (NMR), which is the basis for the
procedure known as MRI (magnetic resonance imaging), to compare the state of water in old (uterine) tissue
and young tissue. Old tissue predictably contains less water than young tissue, but I found that the water
in the old tissue was in a relatively free and uncontrolled state. When tissue swells and takes up water,
more of the water is likely to be in this uncontrolled state, and this is one of the things that makes MRI
so useful, because tumors, for example, show up vividly because of their large amount of uncontrolled
("unbound") water. I suspect that the measurements I made on uterine tissue showed a localized effect, that
opposed the general trend toward increased dryness with aging. In the case of cataracts, this is clearly the
case<strong>: </strong> Most of the lens becomes drier with age, but at a certain point there is a reversal,
and some of the tissue takes up too much water. That"s why I refer to cataracts as a model of age-related
disease, rather than as a model of aging. In this sense, I am including them among the inflammatory diseases
of aging--colitis, arthritis, and cancer, for example. MRI now can show developing cataracts before they are
visible, because of increased water content in the area.
</p>
<p>
The lens of the eye is a fairly dense, tough, transparent living structure, which can develop opaque areas,
cataracts, as a result of old age, poisoning, radiation, disease, or trauma. The varieties of cataract
relate to the causes. Most of the oxidative metabolism of the lens is in or near the epithelial layer that
surrounds it. Old-age cataracts most often begin in this region.
</p>
<p>
Although the efficient oxidative energy metabolism occurs near the surface of the lens, <strong>there is a
constant flow of fluid through the lens,</strong>
entering it mainly in the front and back, and leaving on its "sides" or equator (considering the front and
back as the poles, the direction light passes through). Oxygen and nutrients are supplied to the lens by way
of this circulation of fluid, entering mostly from the aqueous humor in front (which also supplies the
cornea), but also from the vitreous humor behind the lens.
</p>
<p>
When the flow of nutrients and energy is impaired, the organized state of the protein and water system in
the cell is damaged, and an excess of water is taken up by the cells, as the protein content decreases. The
loss of organization causes light to be dispersed, with a loss of transparency.
</p>
<p>
The lens of the eye is usually treated as something so specialized that it is hardly considered to be part
of our living substance, just as dentistry has tended to treat teeth as inert things to be approached
mechanically, rather than physiologically. <strong>The lens"s circulatory system is very interesting,
because of what it says about the nature of living substance. In the absence of blood vessels, it
provides its own flow of nutrients.</strong> This flow is reminiscent of the flow of substances through
the dentine channels of the teeth, through the axons of nerves (two-way transport in a very narrow channel),
and, in some ways recalls the flow of fluids in plants, called "guttation" (drop formation), which is
disturbing to botanists, because it is contrary to the textbook descriptions of proper physiology.
</p>
<p>
<strong>The flow of material through lens cells, dentine canals, and nerve axons should allow us to gain a
perspective in which these observable processes become a model for other biological situations</strong>
in which "transport" occurs<strong>:</strong> Kidney, intestine, or the skin of frogs, for example, in which
water, ions, and other solutes are moved in considerable quantities.
</p>
<p>
When cells metabolize, they create gradients. In the cell, electrical, chemical, osmotic, and thermal
gradients, for example, are constantly being produced or maintained. The whole substance of the cell is
involved in its life processes. Because of prejudices introduced 200 years ago, the life of the cell has
been relegated to its "membrane" (where hypothetical "membrane pumps" reside) and its nucleus. <strong>
When the term "cell" (hollow space) came into use instead of "corpuscle" (little body), a mind-set came
into existence that discounted the importance of most of the living material,</strong> and claimed that
it was a mere "random solution." Random solutions don"t do much. The wonderful "membrane," under the
direction of the nucleus (and its set of instructions), took care of everything.
</p>
<p>
Whenever assimilation or excretion took place, it was explained by inventing a property possessed by the
cell "membranes." Therefore, we have physiology textbooks that have an unfounded explanation for everything.
Before Copernicus, planetary movements were described as arbitrary "epicycles." They didn't make sense, but
people studied them and felt that they were important. "Membrane physiology" is the modern equivalent of the
Ptolemaic epicycles.
</p>
<p>
We know that glucose can be metabolized into pyruvic acid, which, in the presence of oxygen, can be
metabolized into carbon dioxide. Without oxygen, pyruvic acid can be converted into lactic acid. The
production of lactic acid tends to increase the pH inside the cell, and its excretion can lower the pH
outside the cell.
</p>
<p>
The decrease of carbon dioxide that generally accompanies increased lactic acid, corresponds to increased
intracellular pH. Carbon dioxide binds to many types of protein, for example by forming carbamino groups,
changing the protein conformation, as well as its electrical properties, such as its isoelectric point. With
increased pH, cell proteins become more strongly ionized, tending to separate, allowing water to enter the
spaces, in the same way a gel swells in an alkaline solution.
</p>
<p>
The Bohr-Haldane effect describes the fact that hemoglobin releases oxygen in the presence of carbon
dioxide, and releases carbon dioxide in the presence of oxygen. When oxygen is too abundant, it makes
breathing more difficult, and one of its effects is to cause carbon dioxide to be lost rapidly. At high
altitude, more carbon dioxide is retained, and this makes cellular respiration more efficient.
</p>
<p>
The importance of carbon dioxide to cell control process, and to the structure of the cell and the structure
of proteins in general suggested that degenerative diseases would be less common at high altitude. Wounds
and broken bones heal faster at high altitude, but the available statistics are especially impressive in two
of the major degenerative conditions, cancer and cataracts.
</p>
<p></p>
<p>
The two biggest studies of altitude and cataracts (involving 12,217 patients in one study, and 30,565
lifelong residents in a national survey in Nepal) showed a negative correlation between altitude and the
incidence of cataract. At high altitude, cataracts appeared at a later age. <strong>In Nepal, an increase of
a few thousand feet in elevation decreased the incidence of cataracts by 2.7 times. At the same time, it
was found that exposure to sunlight increased the incidence of cataracts, and since the intensity of
ultraviolet radiation is increased with altitude, this makes the decreased incidence of cataracts even
more important.</strong>
</p>
<p>
All of the typical causes of cataracts, aging, poisons, and radiation, decrease the formation of carbon
dioxide, and tend to increase the formation of lactic acid.<strong>
Lactic acid excess is typically found in eyes with cataracts.</strong>
</p>
<p>
The electrical charge on the structural proteins will tend to increase in the presence of lactic acid or the
deficiency of carbon dioxide, and the increase of charge will tend to increase the absorption of water.
</p>
<p>
The lens can survive for a considerable length of time <em>in vitro </em>
(since it has its own circulatory system),<em> </em>
so it has been possible to demonstrate that changes in the composition of the fluid can cause opacities to
form, or to disappear.
</p>
<p>
Oxidants, including hydrogen peroxide which occurs naturally in the aqueous humor, can cause opacities to
form quickly, but they will also disappear quickly in a solution that restores metabolic energy. The lens
regulates itself powerfully<strong>;</strong> for example, it will swell when put into a hypotonic solution,
but will quickly adapt, returning to approximately its normal size.
</p>
<p>
Several years ago, I saw what appeared to be oxidant-induced cataracts. Two women had a very sudden onset of
cataracts, and I asked about their diet and supplements<strong>;</strong> it turned out that one of them had
begun taking 500 mg of zinc daily a few months earlier, and the other had begun taking 600 mg of zinc and
250 mg of iron, on her doctor"s recommendation, just a couple of months before the cataracts appeared.
</p>
<p>
For some reason, there have been many nutritional supplements sold as cataract remedies in the form of eye
drops. I suppose a trace of the material could diffuse through the cornea into the aqueous humor, where it
might make a difference in the lens"s nutrient supply, but it seems more reasonable to treat the body as a
whole, nourishing every part in a balanced way.
</p>
<p>
Besides living at a high elevation or breathing extra carbon dioxide, the most certain way to increase the
amount of carbon dioxide in the eye, and to prevent an excess of lactic acid, is to make sure that your
thyroid function is adequate.
</p>
<p>
One man who took thyroid, USP, and vitamin E told me that his cataracts had regressed, but I haven"t known
other people who tried this.
</p>
<p>
If a person already has distinct cataracts, it might be worthwhile to experiment with a relatively high
degree of hypercapnia, for example, breathing a 5% mixture of CO2 in air.
</p>
<p>
Carbon dioxide, at higher levels than are normal at sea level, has a profound effect on free radicals,
reducing the free radical activity in the blood to approximately zero, before reaching the level that
produces acidosis.
</p>
<p>
There are several situations in which carbon dioxide affects the hydration, water content, of biological
materials, that I think give an insight into its effects on the lens. Hydrophilic glycoproteins are involved
in each case. These are proteins with attached chains of sugar molecules that make them associate with a
large amount of water. In the cornea, increased carbon dioxide strongly protects against swelling. The bulk
of the cornea is a connective tissue that is relatively simple and passive compared to the compact cellular
structure of the lens, and it is conventional to describe the thin layers of cells on the inside and outside
of the cornea as being responsible for the water content of the underlying substance. However, even when the
epithelial cells are removed, it has been demonstrated that carbon dioxide is able to prevent corneal
swelling. (M.V. Riley, et al., "The roles of bicarbonate and CO2 in transendothelial fluid movement and
control of corneal thickness," <em>
Invest. Ophthalmol. Vis. Sci. 36(1),</em> 103-112, 1995.)
</p>
<p>
Bronchial mucous secretions are an even simpler system, so it is very interesting that carbon dioxide is
recognized as the most powerful regulator of their behavior. (This has important implications for "cystic
fibrosis," or mucoviscidosis.) Goodman and Gilman (page 1068, <em>
Pharmacological Basis of Therapeutics,</em> 2nd Edition, Macmillan Co., 1956), say
</p>
<p>
"Among inhalants, steam and carbon dioxide have been found to be excellent expectorants. Relative humidity
above 85 per cent liquefies sputum, decreases its viscosity...." "Carbon dioxide is the most effective agent
of all. It not only lowers the viscosity of tenacious sputum, thereby facilitating expectoration, but it
decreases the volume of sputum by promoting its active resorption by bronchial mucosa." "A five to ten per
cent concentration of carbon dioxide is adequate and well tolerated if administered at intervals." "Oxygen
has been shown to be an antiexpectorant and has effects opposite to those of carbon"
</p>
<p>
Oxygen tends to displace carbon dioxide from tissue, and is a source of free radicals.
</p>
<p>
One of the best-known free radical scavenging substances that has been widely used as a drug is iodide. It
has been used to treat asthma, parasites, syphilis, cancer, Graves" disease, periodontal disease, and
arteriosclerosis. Diseases that produce tissue overgrowth associated with inflammation--granulomas--have
been treated with iodides, and although the iodide doesn"t necessarily kill the germ, it does help to break
down and remove the granuloma. Leprosy and syphilis were among the diseases involving granulomas* that were
treated in this way. In the case of tuberculosis, it has been suggested that iodides combine with
unsaturated fatty acids which inhibit proteolytic enzymes, and thus allow for the removal of the abnormal
tissue.
</p>
<p>
In experimental animals, iodide clearly delays the appearance of cataracts. (Buchberger, et al., 199l.)
</p>
<p>
Inflammation, edema, and free radical production are closely linked, and are produced by most things that
interfere with energy production.
</p>
<p>
Endotoxin, produced by bacteria, mainly in the intestine, disrupts energy production, and promotes
maladaptive inflammation. The wide spectrum of benefit that iodide has, especially in diseases with an
inflammatory component, suggests first that it protects tissue by blocking free radical damage, but it also
suggests the possibility that it might specifically protect against endotoxin.
</p>
<p>
There are subtler differences in transparence that probably have a variety of causes, but differences in
water content or hydration might be involved in the lower transparency that has been seen in women's lenses.
Estrogen, which tends to produce edema and hypotonic body fluids, also increases prolactin production.
Prolactin is involved in water and electrolyte regulation, and it has been found to <strong>accelerate the
development of experimental cataracts.</strong> (M. C. Ng, et al, 1987.) These hormones are associated
with the calcification of soft tissues, and cataracts contain very high levels of calcium. (Avarachan and
Rawal, 1987; Hightower and Reddy, 1982.)
</p>
<p>
Estrogen is strongly associated with free radical processes, calcium mobilization, and acetylcholine
release, all of which are involved in the process of excitoxicity. Alvarez, et al., (1996) have shown a
possible involvement of acetylcholine in calcium mobilization in the lens.
</p>
<p>
Serotonin is another regulatory substance strongly associated with prolactin and estrogen, and it also can
be involved in disrupting the metabolism of the lens. This is one of the potential dangers in using
supplemental tryptophan. (Candia, et al., 1980.)
</p>
<p>
Old age commonly involves some changes in the color of tissues--loss of pigment from hair and skin, with
appearance of new pigment (age pigment, lipofuscin), which may appear as "liver spots." But there is also a
tendency of the toenails, fingernails, teeth, and lenses to turn yellow or brown. Some of this dark material
seems to be age pigment, derived from unsaturated fatty acids, but other components have been identified,
for example, tryptophan from damaged proteins. The Maillard reaction (similar to the browning that occurs in
bread crust) has often been mentioned in relation to aging, and involves the combination of protein amino
groups with sugars. But the browning of the lens tends to be associated with the general age related drying
of the lens, it isn"t irregularly distributed, and it doesn"t significantly harm vision.
</p>
<p>
When I first heard about the age-related browning of the lens, I thought that the experience of colors would
be affected, so I devised a test in which the relative darkness of blue and yellow could be judged in
comparison with a graded strip of shades of grey.
</p>
<p>
After people of ages ranging from 10 to 80 had given exactly the same matches, I realized that the nervous
system probably corrects for the "yellow filter" effect of the brown lens.
</p>
<p>
The browning of tissues will be the subject of another newsletter.
</p>
<p>
Among the interesting causes of cataracts<strong>: </strong>
Tamoxifen and hypotonic fluids, sodium deficiency<strong>;</strong> toxicity of tryptophan<strong>;</strong>
oxidants (metals, hydrogen peroxide, PUFA); diabetes, photosensitizers and sunlight<strong>; </strong>
excess calcium, deficient magnesium. Excess cortisol. Radiation. Arachidonic and linoleic acids in other
situations have been found to block cells' regulation of their water content. Hypothyroidism tends to
increase the activity of serotonin, estrogen, prolactin, calcium, and the tendency of tissues to retain
water, and to decrease the level of ATP.
</p>
<p>
Among the factors that probably have a role in preventing cataracts<strong>: </strong>
Thyroid, progesterone, pregnenolone, vitamin E, iodide, pyruvate. Increasing the carbon dioxide lowers the
cell"s pH, and tends to resist swelling. Palmitic acid (a saturated fat that can be synthesized by our
tissues) is normally oxidized by the lens. Calcium blockers experimentally prevent cataracts, suggesting
that magnesium and thyroid (which also act to exclude calcium from cells) would have the same effect.
</p>
<p>
Thyroid hormone is essential for maintaining adequate carbon dioxide production, for minimizing lactic acid,
cortisol and prolactin, for regulating calcium and magnesium, for avoiding hypotonicity of the body fluids,
and for improving the ratio of palmitic acid to linoleic acid.
</p>
<p>.</p>
<p><strong> </strong></p>
<p>
<strong> </strong>
<strong><h3>REFERENCES</h3></strong>
</p>
<p>
"Inhibition of ionic transport and ATPase activities by serotonin analogues in the isolated toad lens,"
Candia OA; Lanzetta PA; Alvarez LJ; Gaines W, Biochim Biophys Acta (602)2, 389-400, 1980. "Tryptamine,
5-methyltryptamine and 5-methoxytryptamine had dual effects: 1 mM in the posterior bathing solution
depressed the potential difference of the posterior face of the lens, which resulted in an increase in the
translenticular potential difference and short-circuit current; 1 mM in the anterior solution (in contact
with the lens epithelium) produced a quick and pronounced reduction of the potential difference of the
anterior face. This resulted in a 90-100% decline of the translenticular short-circuit current. Serotonin
and tryptamine were then tested for their effect on the ATPases of lens epithelium. Both amines inhibited
the enzymes with tryptamine at 5 mM completely inhibiting all ATPase activity. <strong>Since tryptophan is
transported from the aqueous humor into the lens and may be converted by lens enzymes to serotonin and
tryptamine, these findings may have physiological implications in cataractogenesis."</strong>
</p>
<p>
"Effects of Ca2+ on rabbit translens short-circuit current: evidence for a Ca2+ inhibitable K+ conductance,"
Alvarez LJ; Candia OA; Zamudio AC, Curr Eye Res, 1996 Dec, 15:12, 1198-207. PURPOSE: To characterize the
effects of medium Ca2+ levels on rabbit lens electrical properties. Overall, these results suggest that
<strong>lens Ca2(+)-mobilizing agents (e.g. acetylcholine)</strong> could trigger the inhibition of
epithelial K+ conductance(s) by the direct action of Ca2+ on K+ channels."
</p>
<p>
"Effects of Ca2+ on rabbit translens short-circuit current: evidence for a Ca2+ inhibitable K+ conductance,"
Alvarez LJ; Candia OA; Zamudio AC, Curr Eye Res, 1996 Dec, 15:12, 1198-207. "PURPOSE: To characterize the
effects of medium Ca2+ levels on rabbit lens electrical properties. Overall, these results suggest that lens
Ca2(+)-mobilizing agents (e.g. acetylcholine) could trigger the inhibition of epithelial K+ conductance(s)
by the direct action of Ca2+ on K+ channels."
</p>
<p>
"D600 increases the resistance associated with the equatorial potassium current of the lens," Walsh SP;
Patterson JW, Exp Eye Res, 1992 Jul, 55:1, 81-5 "This effect is similar to that produced by quinine and by a
calcium-free medium, and is attributed to the prevention of an increase in the calcium-dependent conductance
produced by pCMPS."
</p>
<p>
"Effects of hydrogen peroxide oxidation and calcium channel blockers on the equatorial potassium current of
the frog lens," Walsh SP; Patterson JW, Exp Eye Res, 1994 Mar, 58:3, 257-65. "Hydrogen peroxide, in
concentrations of 10-1000 microM, produces two major changes in the current-voltage relationships associated
with the equatorial potassium current of the lens. First, the resting and reversal potentials become more
negative than they were prior to treatment with hydrogen peroxide and second, the membrane resistance
related to the equatorial current is decreased. The shift in the resting and reversal potentials is in the
opposite direction from that produced by ouabain. Based on the Nernst equation, the shift in the reversal
potential suggests that there is an <strong>increase in the concentration of potassium in the lens. The 86Rb
uptake and efflux are increased. These observations suggest that hydrogen peroxide stimulates the
Na,K-pump. The decrease in membrane resistance is inhibited by 100 microM of quinine, a
calcium-dependent potassium channel blocker, and does not decrease in a calcium-free medium. This
suggests that the decrease in resistance may be secondary to an increase in lenticular calcium.</strong>
These effects of hydrogen peroxide are similar to those of p-chloromercuriphenylsulfonate (pCMPS), a nearly
impermeant sulfhydryl binding agent,<strong>
and suggest that permeant hydrogen peroxide may increase calcium influx by acting on sulfhydryl groups
on the outer surface of lens membranes. Verapamil, a calcium channel blocker, is reported to prevent
cataract formation.</strong>"
</p>
<p>
"Effect of prolactin on galactose cataractogenesis," Ng MC; Tsui JY; Merola LO; Unakar NJ phthalmic Res
19:2, 82-94, 1987. "Prolactin has been known to affect the water and electrolyte balance. Because increased
lens hydration has been shown to be a common phenomenon in most, if not all types of cataracts, we have been
interested in investigating a possible role of prolactin in sugar cataract induction and progression. For
this study, we have used morphological and biochemical approaches. The prolactin delivery method involved
intraperitoneal implantation of one or more pellets in Sprague-Dawley female rats. Following implantation of
the desired number of prolactin or control (nonprolactin) pellets, animals were either fed galactose and lab
chow, or lab chow diet. Gross morphological observations of whole lenses, slit-lamp examination of lenses
and light microscopic analysis of lens sections showed that in the galactose-fed prolactin group, galactose
associated alteration progressed faster and total opacification (mature cataract development) was achieved
earlier than in the nonprolactin group. The levels of galactose and dulcitol were higher in the lenses of
galactose-fed prolactin treated rats as compared to lenses from nonprolactin (control) rats. No significant
difference in lens Na+-K+ ATPase activity between the prolactin and nonprolactin group was observed. Our
results indicate that prolactin accelerates galactose-induced cataractogenesis in rats."
</p>
<p>
"A hypothetical mechanism for toxic cataract due to oxidative damage to the lens epithelial membrane,"
Bender CJ Med Hypotheses, 1994 Nov, 43:5, 307-11 Lenticular opacities can be induced by numerous external
agents that <strong>coincide with those that catalyze oxidative damage to lipids.
</strong>One of the consequences of lipid peroxidation is that the affected membrane is rendered more
permeable to protons. A proton leak in the tight epithelium of lens <strong>would uncouple the
Na+/K(+)-ATPases that regulate the water</strong> and ionic content of the bounded tissue. Once
regulatory control of the osmotic pressure is lost, <strong>
the phase state of the</strong> cell's soluble proteins would change, <strong>
leading to refractive changes or, in extreme cases, precipitation</strong>. The same does not occur in
cornea because the stroma is an extracellular polymer blend rather than solution of soluble polymers.
Polymeric phase transitions in the cornea require that divalent cations pass the epithelial membrane, which
can occur only through the action of ionophores.
</p>
<p>
Tsubota K; Laing RA; Kenyon KR Invest Ophthalmol Vis Sci, 1987 May, 28:5, 785-9, <strong>Abnormalities in
glucose metabolism are thought to be among the main causes of cataract formation.
</strong>
The authors have made noninvasive biochemical measurements of the lens that provide information concerning
glucose metabolism in the lens epithelium. The autofluorescence of reduced pyridine nucleotides (PN) and
oxidized flavoproteins (Fp) within the rabbit lens were noninvasively measured as a function of depth using
redox fluorometry. The peak of the autofluorescence at 440 nm (excited at 360 nm) and 540 nm <strong
>(excited at 460 nm) were determined at the lens epithelium. When 8 mM sodium pentobarbital, a known
inhibitor of mitochondrial respiration, was applied to the lens, the autofluorescence peak at 440 nm
increased and that at 540
</strong>
<strong>nm decreased. The 440 nm autofluorescence is thought to be from
</strong>
reduced pyridine nucleotides, whereas the 540 nm autofluorescence is from the oxidized flavoprotein.
Blocking lens respiration with pentobarbital caused an increase in the PN/Fp ratio by a factor of 3 within
3.5 hr after pentobarbital application."
</p>
<p>
[Use of pyrimidine bases and ATP for conservative treatment of early cataracts] Larionov LN Oftalmol Zh,
1977, 32:3, 221-2
</p>
<p>
<hr />
<strong>
high levels of L-lactate and high ratios of L-lactate in the lens/L-lactate in the aqueous</strong>. 2.
Immature cataractous lenses with anterior capsular/subcapsular opacity; intermediate levels of RTP,
intermediate values for the sums of RTP, RDP, and AMP, <strong>high L-lactate levels, and intermediate
values of the ratios of L-lactate in the lens/L-lactate in the aqueous.</strong>"
</p>
<p>
Sulochana KN; Ramakrishnan S; Vasanthi SB; Madhavan HN; Arunagiri K; Punitham R, "First report of congenital
or infantile cataract in deranged proteoglycan metabolism with released xylose," Br J Ophthalmol, 1997 Apr,
81:4, 319-23." "Of 220 children of both sexes below 12 years of age, with congenital or infantile cataract
treated in Sankara Nethralaya, Madras, India, during a period of 2 years, 145 excreted fragments of GAG
(heparan and chondroitin sulphates) in their urine. There was no such excretion among the control group of
50 children. <strong>
The same was found accumulated in the blood and lenses of affected children.</strong>
In addition, xylose was present in small amounts in the urine and blood and xylitol was present in the lens.
There was a significant elevation in the <strong>activity of beta glucuronidase in lymphocytes and
urine,</strong>
when compared with normals. All the above findings suggest deranged proteoglycan metabolism. As the urine
contained mostly GAG fragments and very little xylose, Benedict's reagent was not reduced. This ruled out
galactosaemia.CONCLUSION: An increase of <strong>beta glucuronidase activity might have caused extensive
fragmentation of GAG</strong> with resultant accumulation in the blood and lens and excretion in urine.
Small amounts of xylose may have come from xylose links between GAG and core protein of proteoglycans. Owing
to their polyanionic nature, GAG fragments in the lens might abstract sodium, and with it water, thereby
increasing the hydration of the lens. Excessive hydration and the osmotic effect of xylitol from xylose
might cause cataract. While corneal clouding has been reported in inborn acid mucopolysaccharidosis,
congenital or infantile cataract with deranged metabolism of proteoglycans (acid
mucopolysaccharide-xylose-protein complex) is reported in children for the first time."
</p>
<p>
"State of electrolytes, osmotic balance and the activity of ATPase in the lenses of selenite--induced
cataracts," Avarachan PJ; Rawal UM Indian J Ophthalmol, 1987, 35:5-6, 210-3. "Selenite-cataracts
incorporated many morphological characteristics observed in human senile catracts. Progressive elevation of
sodium, marked loss of potassium, <strong>several fold increment of calcium; considerable loss of magnesium
levels,</strong>
a dose-response reduction of total-ATPase activity <strong>and significant hydration are the important
features</strong> observed in the lens during the progressive treatment of selenite. The
sodium-potassium imbalance is found to be a secondary effect during the development of cataract and is
suggested to bring about by <strong>an abnormal accumulation of calcium ions</strong> and inactivation of
transport enzyme. The calcium activated proteases could be the promoting factor for the proteolysis and
insolubilization of lens proteins in the inducement of selenite cataract. The impact of selenite on the SH
containing ATPase anzymes could be the cause of impairment in energy metabolism, derangement of electrolytes
and osmotic imbalance which, in turn, accelerate the cortical involvement of lens opacities."
</p>
<p>
"Glucose metabolism by human cataracts in culture," Wolfe JK; Chylack LT Jr Exp Eye Res 43:2, 243-9, 1986.
"Metabolism in human senile cataracts has been studied using uniformly labeled [14C]glucose. Intracapsularly
extracted lenses were cultured in TC-199 media with a glucose concentration of 5.5 mM. Results show that
lactate production accounts for 97% of the glucose metabolized. Under these standard incubation conditions
there is negligible accumulation of alpha-glycerol phosphate, glucose-6-phosphate, and sorbitol. The rate of
lactate production was found to be relatively uniform over a range of cataract severities which were
determined from the CCRG classification. The effects of several perturbants in the medium were
measured.<strong>
An ATP concentration of 3 mM was found to inhibit lactate production."
</strong>
</p>
<p>
M. V. Riley, et al., "The roles of bicarbonate and CO2 in transendothelial fluid movement and control of
corneal thickness," Invest. Ophthalmol. Vis. Sci. 36(1), 103-112, 1995. <strong>"The equilibrium thickness
of deepithelialized corneas swollen with HCO-/CO2 on both surfaces was 35 microns less than that of
corneas swollen in HPO4-." "Normal corneal thickness can be maintained in vitro only in media that
contain HCO3- at concentrations of more than 20 mM."</strong>
</p>
<p>
"The effect of X-irradiation on the sodium-potassium-activated adenosine triphosphatase (Na-K-ATPase)
activity in the epithelium of the rat lens. A histochemical and biochemical study," Palva M Acta Ophthalmol
(Copenh), 1978 Jun, 56:3, 431-8. "The epithelial Na-K-ATPase activity of the rat lens was studied after
X-irradiation at intervals of three to ninety days. The enzyme was demonstrated histochemically by light
microscopy and it was measured biochemically by a fluorometric method. Neither histochemical nor biochemical
changes of Na-K-ATPase content of the lens epithelium were observed during the development of cataract. In
whole-mount preparations the enzyme activity was localized in the cell membranes. However, one month after
radiation a few peripheral cells had in addition a precipitated over the whole cell. <strong>The unaltered
Na-K-ATPase</strong>
<strong>
content in the epithelium</strong> suggests that the hydration of the lens after X-irradiation is
primarily caused by <strong>changes in the passive permeability properties of the cell membranes and not by
a decreased capacity of the activity cation pump."
</strong>
</p>
<p>
McNamara NA; Polse KA; Bonanno JA<strong> "Stromal acidosis modulates corneal swelling." </strong>
Invest Ophthalmol Vis Sci, 1994 Mar, 35:3, 846-50 "PURPOSE. Studies have shown that stromal acidosis reduces
the rate of corneal thickness recovery after induced edema, providing the first human in vivo evidence that
corneal pH can influence corneal hydration control. This finding raises the question of the possible effect
that pH may have on induced corneal swelling. To explore this question, the corneal swelling response to
hypoxia was measured while stromal pH was controlled. METHODS. Corneal edema and stromal acidosis was
induced in ten subjects by passing a mixture of nitrogen and carbon dioxide gas across the eyes through
tight-fitting goggles. <strong>One eye of each subject received 100% N2, whereas the contralateral eye
received a mixture of 95% N2 and 5% CO2. Exposures of 95% N2 + 5% CO2 lower pH on average to 7.16 versus
7.34 for 100% N2 alone.</strong> Before and after 2.5 hours of gas exposure, central corneal thickness
(CCT) was measured. RESULTS. <strong>Eyes exposed to the lower pH environment (eg, N2 + CO2) developed less
change in CCT</strong> compared to the eyes receiving N2 alone. Overall increase in CCT was 29.9 +/- 5.3
microns for eyes exposed to the 95% N2 + 5% CO2 gas mixture, versus 37.1 +/- 4.8 microns for 100% N2 <strong
>eyes (P &lt; 0.0001). CONCLUSIONS. The corneal swelling response to hypoxia can be reduced by lowering
stromal pH. Because changes in corneal pH alone have not been found to alter steady-state CCT, it is
proposed that pH
</strong>
exerts its effect only under non-steady-state conditions (ie, corneal swelling and deswelling). This
suggests that acidosis may produce changes in the <strong>rate of lactate metabolism</strong> or alter
endothelial hydraulic conductivity."
</p>
<p>
Buchberger W; Winkler R; Moser M; Rieger G, "Influence of iodide on cataractogenesis in Emory mice,"
Ophthalmic Res, 1991, 23:6, 303-8. Cataract development was studied in two groups of Emory mice by
periodical biomicroscopic examinations (beginning at 5 weeks of age) and by a final evaluation of
water-soluble SH groups in the lenses. The experimental group was given 256 micrograms iodide/kg body weight
with the drinking water throughout the study. The untreated control group received tap water. <strong>Iodide
treatment induced a delay of cataract formation...."</strong> "A still significant difference in the
degree of cataract was also found between the two groups at week 47 of age. No difference was found in the
content of water-soluble SH groups. The results are discussed in relation <strong>to the known antioxidant
and .OH-scavenging effect of iodide and to the oxidative changes in the lens occurring during
progression of cataract development.</strong>"
</p>
<p>
"[The chemical nature of the fluorescing products accumulating in the lipids of the crystalline lenses of
mice with hereditary cataract]," Shvedova AA; Platonov ES; Polianskii NB; Babizhaev MA; Kagan VE Biull Eksp
Biol Med, 1987 Mar, 103:3, 301-4.<strong>
"The content of diene conjugates (lipid hydroperoxides) was shown to be significantly higher in lipids
extracted from the lenses of mice with hereditary cataract than in the controls. The same holds true for
characteristics of fluorescence of the end-product of lipid peroxidation."</strong> "It was established
that high-molecular weight fluorescent fractions corresponded to lipid components of <strong>
lipofuscin-like pigments.</strong> NMR and mass spectrometry of low-molecular weight fractions suggested
that they contained predominantly products of free radical oxidation of <strong>long chain polyunsaturated
fatty acids (C22:6). "</strong>
</p>
<p>
"Formation of N'-formylkynurenine in proteins from lens and other sources by exposure to sunlight," Pirie A
Biochem J, 1971 Nov, 125:1, 203-8.
</p>
<p>
"Lipid fluorophores of the human crystalline lens with cataract." Babizhayev MA Graefes Arch Clin Exp
Ophthalmol, 1989, 227:4, 384-91 "It has been established that the development of cataract is accompanied by
the formation of various fluorophores in the lipid fraction of the lens. These lipid-fluorescing products
have been separated chromatographically according to polarity and molecular weight. It is shown that the
initial stages of the development of cataract are characterized by the appearance of lipid fluorophores in
the near ultraviolet and violet regions of the spectrum <strong>(excitation maximum 302-330 nm, emission
maximum 411 nm) with low</strong> polarity and a small molecular weight; the maturing of the cataract
is<strong>
characterized by an increase in the intensity of the long-wave fluorescence of the lipids in the
blue-green region (430-480 nm) and by the formation of
</strong>
polymeric high-molecular-weight fluorescing lipid products with high polarity. It has been demonstrated that
the appearance of lipid fluorophores in the <strong>crystalline lens is associated with the free radical
oxidative modification of the phospholipids and fatty acids in cataract."
</strong>
</p>
<p>
"Incidence of cataracts in the mobile eye hospitals of Nepal," Brandt F; Malla OK; Pradhan YM; Prasad LN;
Rai NC; Pokharel RP; Lakhe S, Graefes Arch Clin Exp Ophthalmol, 1982, 218:1, 25-7 The incidence of cataract
in Nepal was determined from data collected in 14 mobile eye hospitals (called 'eye camps'). Of a total of
<strong>12,217</strong> patients examined in the out-patient department (OPD), cataract surgery was
performed on 2,163. The percentage of cataract patients in the OPD was <strong>less in the mountains (13.8%)
than in the Tarai plains (19.8%).</strong>
In the inhabitants of the mountains, the majority of whom belong to the Tibeto-Birman race, <strong
>cataracts appeared at a significantly later age in both males and females compared to the people of the
plains, who are mostly Indo-Aryan.</strong> Cataracts were discovered in both groups at a younger age in
women than in men."
</p>
<p>
"Associations among cataract prevalence, sunlight hours, and altitude in the Himalayas." Brilliant LB;
Grasset NC; Pokhrel RP; Kolstad A; Lepkowski JM; Brilliant GE; Hawks WN; Pararajasegaram R., Am J Epidemiol
118:2, 250-64 1983. "The relationship between cataract prevalence, altitude, and sunlight hours was
investigated in a <strong>large national probability sample survey of 105 sites</strong> in the Himalayan
kingdom of Nepal, December 1980 through April 1981. Cataract of senile or unknown etiology was diagnosed by
ophthalmologists in 873 of <strong>30,565</strong>
<strong>full-time life-long residents</strong> of survey sites. Simultaneously, the altitude of sites was
measured using a standard mountain altimeter. Seasonally adjusted average daily duration of sunlight
exposure for each site was calculated by a method which took into account latitude and obstructions along
the skyline. Age- and sex-standardized <strong>cataract prevalence was 2.7 times higher in sites at an
altitude of 185 meters or less than in sites over 1000 meters. Cataract prevalence was negatively
correlated with altitude</strong>
<hr />
</p>
<p>
<strong>"The untenability of the sunlight hypothesis of cataractogenesis</strong>," Harding JJ Doc
Ophthalmol 88:3-4, 345-9, 1994-95. "The excess prevalence of cataract in <strong>third world countries led
early this century to the hypothesis that sunlight causes cataract. The hypothesis, which ignored
differences in diet, culture, poverty and prevalence of other diseases</strong> such as diarrhoea,
received little support until about thirty years ago when biochemical studies were set up to explore the
browning of lens proteins, which is a common feature of cataract on the Indian subcontinent. Initially these
studies were encouraging in that exposure to sunlight caused some changes seen in cataractous lenses, but
eventually the hypothesis was rejected because the first change in the laboratory was the destruction of
tryptophan, <strong>but this was not found in brown cataract lenses.</strong> A brown nuclear cataract could
not be produced artificially in the laboratory using sunlight or UV exposure. Exposure of laboratory animals
has produced lens opacities, but in most experiments the doses required have also caused keratitis,
conjunctivitis, iritis and inflammation. The cornea seems more sensitive than the lens, which is not
surprising, as it gets the first chance to absorb damaging UV. The biochemical rejection of the hypothesis
coincided with the re-start of the epidemiological studies. Most of these are simply latitude studies and
are no more than a repeat of what was available sixty years ago. They do not help to find a cause. <strong
>Two studies showed that cataract was less common at higher altitude in the Himalayas, but unfortunately led
to opposing conclusions</strong>. On the basis of common knowledge that UV exposure was greater at
higher altitude, the first altitude study led to the rejection of the sunlight hypothesis."
</p>
<p>
"Anticataract action of vitamin E: its estimation using an in vitro steroid cataract model," Ohta Y; Okada
H; Majima Y; Ishiguro I Ophthalmic Res, 1996, 28 Suppl 2:, 16-25 "The aim of this study was to estimate the
anticataract action of vitamin E using an in vitro methylprednisolone (MP)-induced cataract model. The same
severity of early cortical cataract was induced in lenses isolated from male Wistar rats aged 6 weeks by
incubation with MP (1.5 mg/ml) in TC-199 medium. The cataractous lenses showed slight increases in lipid
peroxide (LPO) content and Na+/K+ ratio and slight decreases in reduced glutathione (GSH) content and
glyceraldehyde-3-phosphate dehydrogenase (GAP-DH), a sensitive index of oxidative stress, and
Na+,K(+)-ATPase activities. When the cataractous lenses were further incubated in TC-199 medium with and
without vitamin E (250 micrograms/ml) for 48 h, the progression of cataract was prevented in the vitamin
E-treated lenses, but not in the vitamin E-untreated lenses. The vitamin E-untreated lenses showed a
decrease in vitamin E content and an increase in water content in addition to further increases in LPO
content and Na+/K+ ratio and further decreases in GSH content and GAP-DH and Na+,K(+)-ATPase activities. In
contrast, the changes of these components and enzymes except for GSH were attenuated in the vitamin
E-treated lenses. From these results, it can be estimated that vitamin E prevents in vitro cataractogenesis
in rat lenses treated with MP by protecting the lenses against oxidative damage and loss of membrane
function. "
</p>
<p>
"Prevention of oxidative damage to rat lens by pyruvate in vitro: possible attenuation in vivo," Varma SD;
Ramachandran S; Devamanoharan PS; Morris SM; Ali AH,.Curr Eye Res, 1995 Aug, 14:8, 643-9 "Studies have been
conducted to assess the possible preventive effect of pyruvate against lens protein oxidation and consequent
denaturation and insolubilization. Rat lens organ culture system was used for these studies. The content of
water insoluble proteins (urea soluble) increased if the lenses were cultured in medium containing hydrogen
peroxide. Incorporation of pyruvate in the medium prevented such insolubilization. The insolubilization was
associated primarily with loss of gamma crystallin fraction of the soluble proteins. PAGE analysis
demonstrated that insolubilization is related to -S-S- bond formation which was preventable by pyruvate.
Since pyruvate is a normal tissue metabolite the findings are considered pathophysiologically significant
against cataract formation. This was apparent by the <strong>prevention of selenite cataract in vivo by
intraperitoneal administration of pyruvate.</strong>"
</p>
<p>
"Glucocorticoid-induced cataract in chick embryo monitored by Raman spectroscopy," Mizuno A; Nishigori H;
Iwatsuru M Invest Ophthalmol Vis Sci, 30:1, 132-7, 1989. "Glucocorticoid-induced cataract lens in chick
embryo was monitored by laser Raman spectroscopy. The lens opacity that appeared in chick embryo is a
reversible one. Raman spectra show no significant change in the relative content of water or secondary
structure of the proteins upon lens opacification. The intensity ratios of tyrosine doublet bands in Raman
spectra between clear and opaque lens portions are changes. <strong>
This change is reversible,
</strong>and <strong>is interpreted as a protein-water phase separation that occurred during lens
opacification</strong>."
</p>
<p>
"[NMR study of the state of water in the human lens during cataract development]" Babizhaev MA; Deev AI;
Nikolaev GM, Biofizika 30:4, 671-4,1985. "Water proton spin-spin relaxation times (T2) and the content of
bound, "non-freezable" at -9 degrees C water in both normal human lenses and human lenses of different
stages of cataract progression (cataracta incipiens, nondum matura, mature hypermatura) were measured by NMR
spin echoes method. By the stage of cataracta nondum matura, increase of bound water content and
simultaneous, almost half decrease of the relaxation time (T2), were observed. However, on the following
stages of cataract evaluation (almost mature, mature cataracts) <strong>a gradual decrease of bound water
content is noted,
</strong>but only for the mature cataract stage the water content significantly differs from that of the
normal one. On the stage of hypermature cataract the presence of two unexchanged with each other fractions
of water is found. The obtained data are <strong>explained by lens protein reconstructions during the
cataract progression.</strong>"
</p>
<p>
Hightower KR; Reddy VN "Ca++-induced cataract." Invest Ophthalmol Vis Sci, 1982 Feb, 22:2, 263-7 "Cataracts
in cultured rabbit lenses were produced by elevation of internal calcium. Experimental procedures were
successful in increasing levels of total and bound Ca++, often without significant changes in sodium,
potassium, or water content. Although the excess in calcium was predominantly associated with water-soluble
proteins and was freely diffusible, a significant amount was bound to membranes and cytosol water-insoluble
proteins. Thus, in lenses with a 10-fold increase in total Ca++, the bound Ca++ increased twofold, nearly
35% of which remained fixed to water-insoluble and membrane proteins after exhaustive (72 hr) dialysis. In
contrast, over 95% of the Ca++ in water-soluble protein fractions was removed by dialysis."
</p>
<p>
[Use of pyrimidine bases and ATP for conservative treatment of early cataracts] Larionov LN Oftalmol Zh,
1977, 32:3, 221-2.
</p>
<p>
"Noninvasive measurements of pyridine nucleotide and flavoprotein in the lens," Tsubota K; Laing RA; Kenyon
KR Invest Ophthalmol Vis Sci 28:5, 785-9, 1987. "<strong>Abnormalities in glucose metabolism are thought to
be among the main causes of cataract formation.
</strong>
The authors have made noninvasive biochemical measurements of the lens that provide information concerning
glucose metabolism in the lens epithelium. The autofluorescence of reduced pyridine nucleotides (PN) and
oxidized flavoproteins (Fp) within the rabbit lens were noninvasively measured as a function of depth using
redox fluorometry. The peak of the autofluorescence at 440 nm (excited at 360 nm) and 540 nm <strong
>(excited at 460 nm) were determined at the lens epithelium. When 8 mM sodium pentobarbital, a known
inhibitor of mitochondrial respiration, was applied to the lens, the autofluorescence peak at 440 nm
increased and that at 540 nm decreased. The 440 nm autofluorescence is thought to be from
</strong>
reduced pyridine nucleotides, whereas the 540 nm autofluorescence is from the oxidized flavoprotein.
Blocking lens respiration with pentobarbital caused an increase in the PN/Fp ratio by a factor of 3 within
3.5 hr after pentobarbital application."
</p>
<p>
<hr />
<strong>
high levels of L-lactate and high ratios of L-lactate in the lens/L-lactate in the aqueous</strong>. 2.
Immature cataractous lenses with anterior capsular/subcapsular opacity; intermediate levels of RTP,
intermediate values for the sums of RTP, RDP, and AMP, <strong>high L-lactate levels, and intermediate
values of the ratios of L-lactate in the lens/L-lactate in the aqueous."</strong>
</p>
<p>
"Lipid fluorophores of the human crystalline lens with cataract," Babizhayev MA Graefes Arch Clin Exp
Ophthalmol, 1989, 227:4, 384-91. [Initial stages of cataracts are characterized by the fluorescence of the
products of fatty acid free radical oxidation.]
</p>
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