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  • TITLE
  • DEDICATION
  • CERTIFICATE
  • DECLARATION
  • ACKNOWLEDGEMENT
  • List of Abbreviations
  • CONTENTS
  • 1 INTRODUCTION
  • 2 REVIEW OF LITERATURE
  • Fig. 2.2. Proposed mechanism of the diabetogenic action of alloxan
  • Fig. 2.3. Major causes of blindness by economic region
  • Fig. 2.4. Polyol pathway
  • 3 MATERIALS AND METHODS
  • 3.1 EXPERIMENTAL DESIGN
  • 3.1.1 Standardisation of alloxan dose
  • 3.1.2 Histopathology
  • 3.1.3 Preparation of lens extract
  • 3.1.4 Processing of blood samples (Beutler, 1975)
  • (a) Preparation of packed red cell
  • (b) Preparation of 1: 20 hemolysate
  • 3.2 BIOCHEMICAL ANALYSIS
  • 3.2.1 Glucose (Trinder, 1969)
  • 3.2.2 Glycosylated hemoglobin (Chandalia eta/., 1980)
  • 3.2.3 Lens protein glycosylation (Parker 1981)
  • 3.2.4 Hexokinase (EC 2.7.1.1) (Beutler, 1986)
  • 3.2.5 Glucose phosphate isomerase (EC 5.3.1.9) (Beutler, 1986)
  • 3.2.6 Lactate dehydrogenase (EC 1. I .1.27) (Beutler, 1986)
  • 3.2.7 Adenosine triphosphate (Beutler, 1986)
  • 3.2.8 Glucose-6-phosphate dehydrogenase (EC 1.1.1.49) and6-phosphogluconate dehydrogenase (EC 1.1.1.43) (Beutler, 1986)
  • 3.2.9 Transaldolase (EC 2.2.1.2) (Brand, 1983)
  • 3.2.10 Transketolase (EC 2.2.1.1 (Brin, 1974)
  • 3.2.11 Aldose Reductase (EC 1.1.1.21) (Gabbay and Kinoshita, 1975)
  • 3.2.12 Sorbitol dehydrogenase (EC 1.1.1.14) (Scher and Horecker, 1975)
  • 3.2.13 Superoxide dismutase (EC 1.15.1.1) (Paoletti and Mocali, 1990)
  • 3.2.14 Catalase (EC 1.I 1.1.6) (Beutler, 1986)
  • 3.2.15 Glutathione peroxidase (EC 1.11.1.9) (Beutler, 1986)
  • 3.2.16 Reduced glutathione (Beutler, 1986)
  • 3.2.17 Ascorbic acid (Stanley 1979)
  • 3.2.18 Glutathione reductase (EC 1.6.4.2) (Beutler, 1986)
  • 3.2.19 Glutathione-S-transferase (EC 2.5.1.45) (Eeutler, 1986)
  • 3.2.20 Gamma glutamyl transpeptidase (EC 2.3.2.2) (Gowenlock, 1988)
  • 3.2.21 Malonaldehyde (Stocks and Dormandy, 1971)
  • 3.2.22 Diene Conjugate (Lunec 1981)
  • 3.2.23 Hemoglobin (Beutler, 1975)
  • 3.2.24 Proteins (Lowry 1951)
  • 3.3 STATISTICAL ANALYSIS (Rao, 1996)
  • 4 EXPERIMENTAL DIABETOLOGY
  • 4.1 GENERAL FEATURES
  • Fig 4.1 a) Normal rat and b) Diabetic cateract rat
  • Fig. 4.2. Lens weight of rats
  • 4.2 HISTOPATH0LC) GY OF LENS
  • 4.2.1 Results and Discussion
  • Fig. Captions Fig 4.4, Fig 4.5, Fig 4.6, Fig 4.7
  • 4.3 HYPERGLYCEMIA AND DIABETIC CATARACT
  • 4.3.1 Results and Discussion
  • Fig. 4.8. Simplified scheme of glucose metabolism in the lens
  • 4.4 PROTEIN GLYCOSYLATION AND DIABETIC CATARACT
  • 4.4.1 Results and Discussion
  • 4.5 GLYCOLYTIC PATHWAY
  • 4.5.1 Result and Discussion
  • 4.6 THE PENTOSE PHOSPHATE PATHWAY
  • 4.6.1 Results and Discussion
  • 4.7 SORBITOL PATHWAY
  • 4.7.1 Results and Discussion
  • 4.8 OXIDATIVE STRESS
  • 4.8.1 Results and Discussion
  • 4.9 LIPID PEROXIDATION
  • 4.9.1 Results and Discussion
  • 4.10 PROTEIN
  • 4.10.1 Results and Discussion
  • SUMMARY
  • Fig. 5.1 Possible mecanism of diabetic cataractogenesis
  • BIBLIOGRAPHY