Browsing by Author "Pandey, R S"
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Item Activity of glutathione related enzymes and ovarian steroid hormones in different sizes of follicles from goat and sheep ovary of different reproductive stages.(2001-11-22) Sesh, P S; Singh, D; Sharma, M K; Pandey, R SThe investigations on enzymes related to glutathione like glutathione-S-transferase (GST) and glutathione peroxidase (GSH-Px) have been carried out mostly in human and rat ovaries, however the studies on these enzymes in ruminants are relatively absent. In the present study the changes in the activity of these enzymes, in different sizes of follicles from goat and sheep ovaries of different reproductive stages, were investigated. The results demonstrated that the activity of the enzyme GST increased with the increase in size of the follicles from small to large follicles of follicular phase ovary and from small to medium follicles of luteal phase ovary in both the species, thereafter it decreased in large follicles of luteal phase ovary. There was increasing pattern in the activity of GSH-Px in the follicular phase follicles and a decreasing pattern in the luteal phase follicles from both the species. Thus the changes in the activity of glutathione related enzymes namely GST and GSH-Px in different size follicles from both the species during different reproductive phases are evident from the results. It is reasonable, therefore, to assume that these enzymes may have functional role in the steroid hormone metabolism in ruminant ovary as reported in human ovary.Item Biochemical and hormonal characterization of follicles from follicular and luteal phase ovaries of goat and sheep.(1999-05-24) Singh, D; Sharma, M K; Pandey, R SFollicles from goat and sheep ovaries were characterized for their biochemical and hormonal parameters to investigate the effect of developmental stage of follicles on ovarian steroidogenesis. The follicles were isolated mechanically from follicular and luteal phase ovaries and divided in 6 morphologically different groups (small, medium and large follicular and small, medium and large luteal). Follicles were characterized for their contents of protein, DNA, estradiol-17 beta and progesterone and the activity of 3 beta-hydroxysteroid dehydrogenase. There was a progressive increase in the contents of all these biomolecules and activity of the enzyme as size of follicles increased in both the follicular and luteal phase ovaries. Follicles from follicular phase ovaries exhibited higher estradiol-17 beta content than those shown by luteal phase follicles. The reverse pattern was obtained for progesterone content. The results provide the basic data on biochemical and hormonal entities at different stages of follicular development in small ruminants which may be useful for in vitro studies on regulation of follicular development and steroidogenesis.Item Carbonic anhydrase isoenzymes in buffalo erythrocytes: Part I--Purification & some molecular properties.(1983-12-01) Sharma, M K; Pandey, R SItem Carbonic anhydrase isoenzymes in buffalo erythrocytes: Part II--Catalytic properties.(1983-12-01) Sharma, M K; Pandey, R SItem Carbonic anhydrase isoenzymes in buffalo erythrocytes: Part III. Stability and denaturation.(1985-06-01) Sharma, M K; Pandey, R SItem Changes in catalase activity and hydrogen peroxide level in rat ovary during estrous cycle and induction of catalase in rat ovary by estradiol-17 beta.(1998-04-26) Singh, D; Pandey, R SCatalase activity in the whole ovary homogenate and hydrogen peroxide level in the differentially centrifuged fractions of the ovary homogenate during each stage of estrous cycle were measured. The highest catalase activity was observed in the metestrous which declined in the estrous and proestrous and was lowest in the diestrous. An inverse relationship was found between catalase activity and hydrogen peroxide production. Treatment of immature (28-29 days old) female rats with estradiol-17 beta (5 micrograms in 0.2 ml oil/animal/day for consecutive 3 days, s.c.) increased the ovarian catalase activity. The findings indicate that the free radical-scavanger system may have functional role in the ovary.Item Changes in superoxide dismutase activity and estradiol-17 beta content in follicles of different sizes from ruminants.(1998-04-26) Singh, D; Sharma, M K; Pandey, R SSubcellular distribution of oxygen free radical scavenging enzymes has recently been demonstrated in goat ovary. In the present study the follicles of the follicular phase were isolated mechanically from goat and sheep ovaries and grouped as small (< 3 mm), medium (3-6 mm) and large (> 6 mm) follicles. The specific (units/mg protein) and total (units/g tissue) activity of superoxide dismutase (SOD) was estimated in homogenate of different sizes of follicles. The small follicles of both the species contained highest specific and total activity (6.99 +/- 1.49, 107.9 +/- 3.1 in sheep and 3.57 +/- 0.09, 76.5 +/- 4.0 in goat, respectively), whereas large follicles showed lowest specific and total activity (32.02 +/- 0.25, 80.4 +/- 5.5 in sheep and 1.71 +/- 0.06, 63.20 +/- 2.20 in goat, respectively). The estradiol-17 beta was also estimated and expressed as ng/follicle. The results show that estradiol-17 beta content was highest in large follicle (8.00 +/- 0.46 in sheep and 4.5 +/- 0.73 in goat). The content of estradiol-17 beta was increased progessively as the size of the follicles increased. From these findings, an inverse relationship was observed between SOD activity and estradiol-17 beta content in the follicles of different sizes from ruminants which may have functional role in follicle development and steroidogenesis.Item Comparative studies on phosphorylases of the muscle of some vertebrates.(1979-06-01) Patnaik, S K; Supakar, P C; Pandey, R S; Samantisinghar, A; Amar, A; Singh, MItem Comparative study of foetal & adult haemoglobins of buffalo towards denaturation behaviour in acid & alkali.(1977-08-01) Bachlaus, N K; Pandey, R SItem Conformation of chromatin of the skeletal muscle of developing rats and its modulation by sodium butyrate.(1987-06-01) Pandey, R S; Kanungo, M SItem Control of bancroftian filariasis in a rural area through selected treatment with diethylcarbamazine.(1987-12-01) Sharma, S P; Biswas, H; Pandey, D S; Pandey, R S; Das, M; Sharma, G KItem Differential effects of chronic endosulfan exposure to male rats in relation to hepatic drug metabolism and androgen biotransformation.(1989-08-01) Singh, S K; Pandey, R SChronic endosulfan exposure in rats led to considerable increase in the activities of drug metabolizing enzymes, whereas it had inhibitory effect on the activities of enzymes involved in the androgen biotransformation. Endosulfan also produced a dose- and duration-dependent increase in microsomal lipid peroxidation. The alterations produced after shorter duration showed much variation with respect to the dose levels and exposure period of endosulfan studied. The above biochemical changes were reversed after endosulfan withdrawal.Item Effect of insulin-like growth factor-1 on steroidogenesis in cultured carp ovarian follicles: interactions with estradiol.(1999-02-21) Behl, R; Pandey, R SThe biological action of insulin like growth factor-1 (IGF-1) on follicular steroidogenesis during follicular development in common carp was examined. Studies were carried out by culturing small (1-2 mm diam.) and large (> 2 mm diam.) follicles. IGF-1 (0.3-100 ng/ml) had no effect on progesterone accumulation or aromatase activity during 48 hr culture of small follicles. Progesterone accumulation by large follicles was also unaffected by IGF-1 over the same period, although aromatase activity was stimulated in a dose dependent manner (8-fold increase over basal levels with a maximum stimulatory dose of 30 ng IGF-1/ml). In contrast, small and large follicles responded to IGF-1 in terms of both progesterone accumulation and aromatase activity after longer periods of culture (4 days for progesterone and 6 days for aromatase). Concurrent treatment of small follicles with estradiol (10(-7) M) enhanced the action of IGF-1 on both indices of steroidogenesis and advanced the time at which IGF-1 stimulated activity was first detectable. The effect of estradiol on follicular IGF-1 responsiveness were independent of cell number. In summary, these results demonstrate varied actions of IGF-1 carp ovarian follicular steroidogenesis in vitro. The results indicate that carp follicles acquire responsiveness to IGF-1 in terms of aromatase activity during follicular development in vivo and that estradiol can induce the response in vitro. The results also suggest that estrogen and progesterone biosynthesis by cultured carp ovarian follicles is differentially regulated by IGF-1. Together, these results provide new insights into the biological actions of IGF-1 in fish ovary.Item Effect of sub-chronic endosulfan exposures on plasma gonadotrophins, testosterone, testicular testosterone and enzymes of androgen biosynthesis in rat.(1990-10-01) Singh, S K; Pandey, R SInsecticide endosulfan significantly inhibited testicular androgen biosynthesis in adult rats, when fed (po) at 7.5 and 10 mg/kg body weight dose levels, consecutively for 15 and 30 days. No appreciable alterations were apparent in body weights, testicular wet weights, and cytosolic and microsomal protein contents of testis in treated rats. Profound decrease in the levels of plasma gonadotrophins (FSH and LH) along with plasma testosterone and testicular testosterone were observed at both the doses of endosulfan, particularly after the longer exposure of 30 days. Activities of steroidogenic enzymes studied (3 beta- and 17 beta-hydroxysteroid dehydrogenases) were considerably lowered on longer exposure of endosulfan. A significant decrease in the contents/activities of microsomal cytochrome P-450 and related mixed function oxidases (MFOs) in testis of treated rats was also observed, along with a marked inhibition in the activity of cytosolic conjugation enzyme, glutathione-S-transferase at both doses studied. These biochemical changes were reversed when the endosulfan treatment was withdrawn.Item Epidemiological investigation on Japanese encephalitis outbreak in Uttar Pradesh during 1988.(1988-12-01) Narasimham, M V; Rao, C K; Bendle, M S; Yadava, R L; Johri, Y C; Pandey, R SItem Ethanol potentiates in vivo hepatotoxicity of endosulfan in adult male rats.(1991-11-01) Singh, S K; Pandey, R SIn an attempt to evaluate the effect and interaction of ethanol on endosulfan-induced hepatotoxicity in vivo to adult male rats, both, endosulfan (7.5 mg/kg body wt) and ethanol (1.5 g/kg body wt) were studied separately as well as in combination after a chronic oral exposure of 30 days. When fed separately, both the agents were found to induce microsomal mixed function oxidase (MFO) system in treated animals. A simultaneous induction in the activity of cytosolic GSH-s-transferase was found to be associated with significantly induced ascorbate-induced microsomal lipid peroxidation. Both endosulfan and ethanol showed increasing trends in the activities of reducing equivalent (NADPH)-generating enzymes in liver. The activity of hepatic alcohol dehydrogenase was, however, found to be relatively unaffected. When ethanol was administered in combination with endosulfan, the observed effects on the activities of major drug metabolizing enzymes, microsomal lipid peroxidation and NADPH generation were further pronounced. Findings demonstrated the MFO inducing capability of both endosulfan and ethanol, and showed further that chronic ethanol ingestion might potentiate the in vivo hepatotoxicity of endosulfan if administered in combination.Item Genetic polymorphism of serum transferrins in zebu & cross-bred cattle.(1977-01-01) Prasad, S K; Pandey, R S; Shanker, V; Nair, K G; Nair, P GItem Glutathione-S-transferase in rat ovary: its changes during estrous cycle and increase in its activity by estradiol-17 beta.(1996-11-01) Singh, D; Pandey, R SGlutathione-S-transferases (GSTs) are drug metabolizing and detoxification enzymes, involved in the intracellular transport and metabolism of steroid hormones. This study indicated that the enzyme was heterogeneously distributed and changed during estrous cycle. The enzyme was found to be predominantly located in the cytosolic fraction while considerable activity was also observed in the mitochondrial and microsomal fractions. The activity of GST was measured during different stages of estrous cycle, viz proestrous, estrous, metestrous and diestrous. The change in its activity was observed during different stages of estrous cycle. Estrous stage was observed to have the highest GST activity. Immature (28-29 days old) rats treated with estradiol-17 beta (5 micrograms in 0.2 ml oil/animal/day, and 10 micrograms in 0.2 ml oil/animal/day, for 3 days), ovarian GST activity seemed to increase significantly (P < 0.01). This increase in the activity and the heterogeneous distribution of GST indicates the functional role of this enzyme in the ovary under endocrine regulation.Item Gonadal toxicity of short term chronic endosulfan exposure to male rats.(1989-04-01) Singh, S K; Pandey, R SEndosulfan was studied for its effect on rat testicular toxicity in relation to the enzymes of androgen biosynthesis, viz. 3 beta-hydroxysteroid dehydrogenase (EC 1.1.1.145, 3 beta-HSD) and 17 beta-hydroxysteroid dehydrogenase (EC 1.1.1.64, 17 beta-HSD); cytosolic conjugation enzyme, glutathione-S-transferase (EC 2.5.1.18); and testicular as well as serum testosterone levels at the dose levels of 2.5, 5.0, 7.5 and 10 mg/kg body weight fed orally for 7 and 15 days. Organ and body weights of the treated animals did not change significantly, however, the testicular protein contents were found to be increased appreciably after 7 days treatments. The activity profile of cytosolic conjugation enzyme showed much remained low during 7 days treatment, however, the two steroidogenic enzymes showed much individual variations in response to endosulfan treatments. An overall varied response with respect to testosterone biosynthesis and its secretion to serum was observed suggesting nevertheless, a profound hormonal imbalance caused by this insecticide to male gonads on short term chronic exposures.Item Immuno-chemical studies on seminal plasma of goats.(1978-11-01) Prasad, S K; Pandey, R S; Nair, P G