|
OcuPhase
Cataracts are the leading
cause of blindness, accounting for about 42 percent of all cases
of blindness worldwide (affecting about 17 million people). Twenty-eight
thousand new cases are reported everyday. About 20 percent of
all people over 60 have at least the beginning of a cataract
in one or both eyes, and that figure rises to 80 percent for
people over 75.
The most common type of
cataract — a nuclear cataract — is characterized
by a cloudy haze inside the lens. This haze is the physical manifestation
of a random clumping together of the once beautifully ordered
arrangement of lens proteins called crystallins. As the cataract
develops in size and density, it reduces the amount of light
that passes through the lens and scatters the light that does
get through. Thus, instead of all the light rays being focused
precisely to a point on the retina, forming a sharp, clear image
of what we are seeing, many of the rays are spread out across
the retina, forming a fuzzy image. Colors may be dulled or distorted,
and there may be an annoying halo of light around bright objects,
causing a glare effect.
Causes of cataracts include cumulative ultraviolet radiation damage
from sun exposure, heredity, poor nutrition, smoking, high
blood pressure, kidney disease, diabetes, and the long-term
use of corticosteroids (the last two are major risk factors
for cataracts). Oxidative free radicals produced by the above-listed
causes are thought to damage vital biomolecules, including
lipids and proteins, resulting in the clumping together of
these proteins. The antidote to free radicals, of course, is
antioxidants, such as glutathione, lipoic acid, and vitamins
C and E. Consequently, many scientists believe that abundant
consumption of antioxidants may delay the onset of cataracts.
Good nutrition is a key element of effective prevention for most
age-related diseases, and cataracts are no exception. A number
of nutrients can benefit our eyes, and may help prevent diseases
such as cataracts, glaucoma, and macular degeneration. These
nutrients include the tripeptide glutathione (the most abundant
and important antioxidant in the human body, critical for protecting
the lens from free radical damage); vitamins A and C; vitamin
E and some of the B vitamins; various bioflavonoids (especially
quercetin and hesperidin) and carotenoids (especially lutein
and zeaxanthin); the amino acids taurine, N-acetylcysteine
(a precursor of glutathione), and acetyl L-carnitine; the hormone
melatonin; the alkaloid vinpocetine; the herbs bilberry, ginkgo,
and garlic; the minerals zinc and selenium; and, last but certainly
not least, the saturated fatty acid, lipoic acid (“the
antioxidant’s antioxidant”), which plays a central
role in maintaining the body’s antioxidant network.1
Carnosine — a dipeptide consisting of two amino acids (alanine
and histidine) connected to each other by a chemical bond called
the peptide bond — is one of the most exciting anti-aging
nutrients that has recently become widely available.2 Based on
research performed mainly by Russian scientists, it is believed
that carnosine is effective both in preventing and treating cataracts.3-6
The ability of carnosine
to prevent and treat cataracts is believed to be due to its antioxidant
properties and its ability to inhibit a chemical process called
glycation. Glycation leads to deleterious substances called AGEs
(advanced glycation end products). AGEs are chemical complexes
that result from common but undesirable reactions between blood
sugars, such as glucose, and proteins in many parts of our bodies,
including the lenses of our eyes. The sugar-protein complexes
become chemically cross-linked and degrade cellular functions.
The aptly named AGEs are thought to be an important factor in
the aging process.
Carnosine-containing eye
drops have demonstrated efficacy in treating a variety of ophthalmic
conditions, including corneal diseases, cataracts, glaucoma,
and increased intraocular pressure. In 1997, clinical trials
with carnosine-containing eye drops were conducted on 109 ophthalmic
patients. The results confirmed accelerated healing of corneal
erosions, trophic keratitis, post-herpetic epitheliopathy, primary
and secondary corneal dystrophy, and bullous keratopathy.7 Most
striking, however, was the ability of carnosine to eliminate
existing cataracts.8
Carnosine eye drops have
been shown to delay vision senescence in humans, being effective
in 100 percent of cases of primary senile cataract and 80 percent
of cases of mature senile cataract. Scientists concluded that “carnosine
seems to delay the impairment of eyesight with aging, effectively
preventing and treating senile cataract and other age-related
diseases.”9 Carnosine actually restores the proteins in
the lens by removing cross-linked carbonyl groups, and is thought
to function as a “molecular water pump,” thereby
also helping to lower intraocular pressure.10 In earlier experiments
it was demonstrated that applying carnosine to the conjunctiva
(the membrane covering the eye) caused a decrease in normal intra-ocular
pressure and reduced prostaglandin-induced ocular hypertension
(related to glaucoma) in rabbits.11
Some scientists believe
that carnosine is ineffective if it is metabolized (broken down)
by the enzyme, carnosinase. However, studies of corneal transplants
in rabbits that were treated with one of the metabolites of carnosine,
histidine, indicates that the metabolite itself may be bioactive.
Five percent histidine ointment was applied twice daily to 6
transplants for two months. All six transplants healed and were
clear. On the other hand, transplants which were treated with
daily applications of one percent cortisone became opaque, necrotic,
and failed to heal. Likewise, transplantation failed completely
in six control eyes.12 This indicates that histidine may be an
active portion—if not the active factor—of the carnosine
molecule.
N-acetylcarnosine
(NAC), like its parent
compound, carnosine,
occurs naturally
throughout the human
body. Both compounds
are found primarily
in the heart and
skeletal muscles
(the word carnosine
is derived from the
Latin word for flesh)
and in the brain.
Carnosine was discovered
in 1900 in Russia,
and it is in Russia
that most of the
recent research on
the N-acetylcarnosine
derivative has been
carried out.13-15
Research with N-acetylcarnosine,
as with carnosine,
demonstrates that
it is effective not
only in preventing
cataracts but also
in treating them.
NAC has been shown
to improve vision
by partially reversing
the development of
the cataract, thus
increasing the transmissivity
of the lens to light.
The structural difference
between NAC and carnosine is that one hydrogen atom in carnosine
replaces an acetyl group (CH3CO-), and this substitution occurs
at a nitrogen atom. An important chemical difference between
carnosine and N-acetylcarnosine is that carnosine is relatively
insoluble in lipids (fats and fatty compounds), whereas N-acetylcarnosine
is relatively soluble in lipids (as well as in water).
This means that N-acetylcarnosine
may pass through the lipid membranes of the corneal and lens
cells more easily than carnosine, and may thereby gain access
more readily to the cells’ interior, which is primarily
aqueous. There, the N-acetylcarnosine is gradually broken down
to carnosine (and, perhaps, to histidine), which then exerts
its beneficial effects.
In one study, Russian scientists conducted two randomized, double-blind,
placebo-controlled trials of 6-months and 24-months duration, with
eye drops consisting of a one percent aqueous solution of NAC administered
as two drops twice daily.16 They treated a total of 49 elderly
patients (average age 65) with cataracts ranging in severity from
minimal to advanced (but not to the point of requiring surgery);
the total number of eyes affected was 76. Using a variety of sophisticated
optical techniques, they monitored the condition of the cataracts,
visual acuity, and glare sensitivity.
The eyes treated with
NAC were substantially improved in 6 months: the measured transmissivity
of the lenses increased in 42 percent of the eyes, by 12-50 percent;
in 90 percent of the eyes, visual acuity improved by 7-100 percent;
and in 89 percent of the eyes, glare sensitivity improved by
27-100 percent. These improvements were sustained for the duration
of the 24-month trial. In no eyes was any worsening of the condition
seen. By contrast, the condition of the untreated eyes in the
control group worsened. Visual acuity dropped in 89 percent of
the controls by 17-80 percent after 24 months.
Another interesting study
by the same team also evaluated patients between the ages of
48 and 60, who had various degrees of eyesight impairment, but
who did not have the symptoms of cataract. After a course of
treatment ranging from 2 to 6 months, the conclusion was that
the eye drops alleviated eye-tiredness and continued to improve
eyesight (i.e. there was more clear vision). The subjects reported
that the treatment “brightened” and “relaxed” their
eyes. This is an important indicator that the eye drops have
a value both for preventive purposes, as well as medical applications.
Carnosine and N-acetylcarnosine eye drops appear to be a safe,
effective means to prevent cataracts, and to possibly even
treat cataracts that are forming. Although cataract surgery
is safe and highly effective, the use of topical carnosine
or NAC eye drops may give many people another option.
References
1. Block, W. N-Acetylcarnosine
May Help with Cataracts. NAC eye drops show benefits in both preventing
and treating this age-related condition. LE Magazine, Aug. 2003.
2. Bourassa, D., and Dean, W. M.D. Carnosine: A Remarkable Multipurpose
Anti-Aging Nutrient. Vitamin Research News, Vol. 14., Num. 11,
Nov. 2000.
3. Babizhayev MA, Deyev A. Free radical oxidation of lipid and
thiol groups in genesis of cataract. Biophysics (biofizika), 1986,
31, 119-125, Pergamon Journals Ltd.
4. Babizhayev MA, Deyev Al, Linberg LF. Lipid peroxidation as a
possible cause of cataract. Mech. Ageing Dev. 1988, 44, 69-89.
5. Babizhayev MA, Antioxidant activity of L-carnosine, a natural
histidine-containing di-peptide in crystalline lens. Biochem. Biophys.
Acta., 1989a, 1004, 363-371.
6. Babizhayev MA, Deyev A. Lens opacity induced by lipid peroxidation
products as a model of cataract associated with retinal disease.
Biochim. Biophys. Acta., 1989b, 1004, 124-133.
7. Maichuk, IUF, Formaziuk, VE, Sergienko, VI. Development of carnosine
eyedrops and assessing their efficacy in corneal diseases. Vestn
Oftalmol, 1997, 113(6): 27-31.
8. Yuneva, M.O., Bulygina, E.R., Gallant, S.C., et al. Effect of
carnosine on age-induced changes in senescence-accelerated mice.
J Anti-Aging Medicine, 2: 1999, 337-342.
9. Wang AM, Ma C, Xie H, and Shen, F. Use of carnosine as a natural
anti-senescence drug for human beings. Biochemistry, 2000, 65(7),
869-871.
10. Baslow, MH. Function of the N-acetyl-L-histidine system in
the vertebrate eye. Evidence in support of a role as a molecular
water pump. J Mol Neurosci, 1998, 10(3), 193-208.
11. Ermakova, V.N., Babizhaev, M.A., Bunin, A.Ya. Effect of L-carnosine
on intraocular pressure. Byull. Eksp. Biol. Med. 1988, 105(4),
451-453.
12. Borioni, D., and Scassellati-Sforzolini, G. The action of p-aminobenzoic
acid, histidine, and cortisone on the success of corneal transplants,
Am J Ophthalmol, 1953, 36: 575-576.
13. Babizhayev MA, Yermakova VN, Sakina NL, Evstigneeva RP, Rozhkova
EA, Zheltukhina GA. N-Acetylcarnosine is a prodrug of L-carnosine
in ophthalmic application as antioxidant. Clin. Chim. Acta., 1996,
254, 1-21.
14. Babizhayev MA, Yermakova VN, Deyev Al, Seguin M-C. Imidazole-containing
peptiomimetic NAC as a potent drug for the medicinal treatment
of age-related cataract in humans. J. Anti-Aging Medicine 2000a,
2, 43-62.
15. Babizhayev MA, Yermakova VN, Semiletov yu A, Deyev A. The natural
histidine-containing di-peptide N-acetylcarnosine as an antioxidant
for ophthalmic use. Biochemistry (Moscow), 2000b, 65, 588-598.
16. Babizhayev MA, Deyev AI, Yermakova VN, Semiletov YA, Davydova
NG, Kurysheva NI, Zhokotskii AV, Goldman IM. N-Acetylcarnosine,
a natural histidine-containing dipeptide, as a potent ophthalmic
drug in treatment of human cataracts. Peptides, 2001, 22: 979-94.
|