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Lycopene prevents sugar-induced morphological changes and modulates antioxidant status of human lens epithelial cells

Published online by Cambridge University Press:  09 March 2007

Ipseeta Mohanty
Affiliation:
Department of Pharmacology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110029, India
Sujata Joshi
Affiliation:
Department of Pharmacology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110029, India
Deepa Trivedi
Affiliation:
Department of Pharmacology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110029, India
Sushma Srivastava
Affiliation:
Department of Pharmacology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110029, India
S. K. Gupta*
Affiliation:
Department of Pharmacology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110029, India
*
*Corresponding author: Professor S. K. Gupta, fax +91 11 686 2663, email skgupta@hotmail.com
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Abstract

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Cataract is a multifactorial disease. Osmotic stress, together with weakened antioxidant defence mechanisms, is attributed to the changes observed in human diabetic cataract. Epidemiological studies provide evidence that nutritional antioxidants slow down the progression of cataract. The usefulness of lycopene, a dietary carotenoid, in the pathogenesis of human cataracts has not been studied so far. Since the epithelium is the metabolic unit of the lens, the effect of lycopene on galactose-induced morphological changes and antioxidant status of human lens epithelial cells (HLEC) in culture was evaluated in the present study. HLEC of fresh cadaver eyes obtained from an eye bank were cultured in medium supplemented with fetal calf serum (200 ml/l). On confluency, the cells were subcultured in medium containing either 30 m-d-galactose or 30 mM-d-galactose + lycopene (5, 10 or 20 μM) for 72 h. The cells were observed under the phase-contrast microscope and transmssion electron microscope for any morphological changes and then harvested for the estimation of various biochemical variables. Malondialdeyde, glutathione and antioxidant enzymes were significantly altered in the control as compared with the normal cultures. Vacuolization was also observed in the presence of galactose. Addition of lycopene confers significant protection against these changes in HLEC.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2002

References

Aebi, H (1974) Catalase. In Methods of Enzymatic Analysis, vol. 2, [Bergmayer, HE, editor]. London: Academic Press.Google Scholar
Bermbach, G, Mayer, U & Naumann, G (1991) Human lens epithelial cells in tissue culture. Experimental Eye Research 52, 113119.CrossRefGoogle ScholarPubMed
Clinton, SK (1998) Lycopene: Chemistry, biology and implications for human health and disease. Nutrition Reviews 56, 3551.CrossRefGoogle ScholarPubMed
Collier, A & Small, M (1993) The role of polyol pathway in diabetes mellitus. Journal of Hospital Medicine 45, 3840.Google Scholar
Di Mascio, P, Kaiser, S & Sies, H (1989) Lycopene is the most efficient biological carotenoid singlet oxygen quencher. Archives of Biochemistry and Biophysics 274, 17.CrossRefGoogle ScholarPubMed
Eguchi, G & Okada, TS (1971) Ultrastructure of the differentiated colony derived from a single isolated chondrocyte in in vitro culture. Development Growth and Differentiation 12, 297312.CrossRefGoogle Scholar
Hebig, H (1974) Glutathione-S-transferase, the first enzymatic step in mercapturic acid formation. Journal of Biochemistry 249, 71307134.Google Scholar
Jacques, PF & Chylack, LT (1991) Epidemiological evidence of a role for the antioxidant vitamins and carotenoids in cataract prevention. American Journal of Clinical Nutrition 53, 352.CrossRefGoogle ScholarPubMed
Jasmina, BM, Bekhor, I, Weiss, MH & Zlokovic, BV (1994) Galactose induced cataract formation in guinea pigs: Morphological changes and accumulation of galactitol. Investigative Ophthalmology and Visual Science 35, 804811.Google Scholar
Kador, PF & Kinoshita, JH (1984) Diabetic and galactosemic cataracts. Ciba Foundation Symposium 106, 110115.Google Scholar
Lin, LR, Reddy, VN, Giblin, FJ, Kador, PF & Kinoshita, JH (1991) Polyol accumulation in cultured human lens epithelial cells. Experimental Eye Research 52, 93100.CrossRefGoogle ScholarPubMed
Lowry, OH, Rosebrough, NJ & Farr, AI (1951) Protein measurements with the Folin phenol reagent. Journal of Biological Chemistry 193, 265275.CrossRefGoogle ScholarPubMed
Lyle, BJ, Mares Perlman, JA, Klain, R, Palta, M, Bowen, PE, Palta, M, Bowen, PE & Greger, JL (1999) Serum carotenoids and tocopherols and incidence of age related nuclear cataract. American Journal of Clinical Nutrition 69, 272279.CrossRefGoogle ScholarPubMed
Miyoshi, EKN, Fukuda, M & Akagi, Y (1999) Cataract formation through the polyol pathway is associated with free radical production. Experimental Eye Research 68, 457464.Google Scholar
Moron, MS, Depierre, JW & Manmerik, B (1979) Level of glutathione, glutathione reductase and glutathione-S-transferase activity in rat lung and liver. Biochimica et Biophysica Acta 82, 6778.CrossRefGoogle Scholar
Obrosova, IG, Fathallah, L & Lang, HJ (1999) Interaction between osmotic and oxidative stress in diabetic precataractous lens. Biochemical Pharmacology 58, 19451954.CrossRefGoogle ScholarPubMed
Ohkawa, H, Ohishi, N & Yagi, K (1979) Assay of lipid peroxide in animal tissue by thiobarbituric acid reaction. Analytical Biochemistry 95, 351358.CrossRefGoogle ScholarPubMed
Paglia, DE & Valentine, WN (1967) Studies on the quantitative and qualitative characterization of erythrocyte peroxidase. Journal of Laboratory and Clinical Medicine 2, 158.Google Scholar
Pollack, A, Oren, P, Stark, AH, Eisner, Z, Nyska, A & Madar, Z (1999) Cataract development in sand and galactosemic rats fed a natural tomato extract. Journal of Agriculture Food Chemistry 47, 51225126.CrossRefGoogle Scholar
Pollack, A, Madar, Z, Eisner, Z, Nyska, A & Oren, P (19961997) Inhibitory effect of lycopene on cataract development in galactosemic rats. Metabolic Pediatric Systemic Ophthalmology 19–20, 3136.Google ScholarPubMed
Reddy, VN, Agata, K & Sawada, K (1991) Study of crystallin expression in human lens epithelial cell during differentiation in culture and in non-lenticular tissues. Experimental Eye Research 53, 367374.CrossRefGoogle ScholarPubMed
Reddy, VN, Arita, T & Lin, LR (1988) Differentiation of human lens epithelial cells in tissue culture. Experimental Eye Research 47, 905910.CrossRefGoogle Scholar
Spector, A (1995) Oxidative stress induced cataract: Mechanism of action. FASEB Journal 9, 11731182.CrossRefGoogle ScholarPubMed
Stahl, W, Sundquist, AR, Hanusch, M, Schwarz, W & Sies, H (1993) Separation of beta-carotene and lycopene geometrical isomers in biological samples. Clinical Chemistry 39, 810814.CrossRefGoogle ScholarPubMed
Varma, SD, Devamanoharan, PS & Morris, SM (1990) Photoinduction of cataracts in rat lens in vitro: preventive effect of pyruvate. Experimental Eye Research 50, 805812.CrossRefGoogle ScholarPubMed
Varma, SD, Schocket, SS & Richards, RD (1979) Implications of aldose reductase in cataract in human diabetes. Investigative Ophthalmology and Visual Science 3, 237241.Google Scholar
Wolff, SP & Dean, RT (1985) Glucose autoxidation and protein modifications. The potential role of autoxidative glycosylation in diabetes. Biochemical Journal 245, 243250.CrossRefGoogle Scholar
Yeum, KJ, Shang, FM, Schalch, WM, Russell, RM & Taylor, A (1999) Fat soluble nutrient concentrations in different layers of human cataractous lens. Current Eye Research 19, 502505.CrossRefGoogle ScholarPubMed