C Haldar-Misra

Bio: C Haldar-Misra is an academic researcher. The author has contributed to research in topics: 5-Methoxytryptamine & Melatonin. The author has an hindex of 2, co-authored 2 publications receiving 73 citations.

Effect of 5-methoxytryptophan and 5-methoxytryptamine on the reproductive system of the male golden hamster

Abstract: S.c. injections of 25μg of methoxytryptamine (5-MT) in oil into adult male hamsters given between 4.30 and 5 p.m. (light on from 5 a.m. to 7 p.m.: 14 L/10 D) for 51 consecutive days caused involution of the testes. Similar injections of 5-MT given between 8.30 and 9.30 a.m. completely failed to cause regression of the gonads. Under the same conditions, 5-methoxytryptophan (5-MTP) did not induce gonadal atrophy, neither in the morning nor in the late afternoon. These results indicate that, like melatonin, 5-methoxytryptamine is implicated in the control of the reproductive function.

The independency of an intact pineal gland of the inhibition by 5-methoxytryptamine of the reproductive organs in the male hamster.

Abstract: Subcutaneous injections fo 25 micrograms of 5-methoxytryptamine (5-MT) in oil into intact and pinealectomized male hamsters given between 4.30 p.m. and 5 p.m. (light on from 5 a.m. to 7 p.m.; 14 L/10 D) for 54 consecutive days caused involution of the testes. 5-MT, however, is more effective when the pineal is present. These results indicate that melatonin is not the only pineal factor inducing gonadal atrophy in the hamster. 5-MT seems even more effective than melatonin in so far as it is, contrary to melatonin under the same experimental conditions, also effective in the absence of the pineal. Like melatonin, 5-MT appears to be implicated in the control of the reproductive function.

2-[125I]iodomelatonin binding sites in hamster brain membranes: pharmacological characteristics and regional distribution

Abstract: Studies in a variety of seasonally breeding mammals have shown that melatonin mediates photoperiodic effects on reproduction. Relatively little is known, however, about the site(s) or mechanisms of action of this hormone for inducing reproductive effects. Although binding sites for [3H]melatonin have been reported previously in bovine, rat, and hamster brain, the pharmacological selectivity of these sites was never demonstrated. In the present study, we have characterized binding sites for a new radioligand, 2-[125I]iodomelatonin, in brains from a photoperiodic species, the Syrian hamster. 2-[125I]Iodomelatonin labels a high affinity binding site in hamster brain membranes. Specific binding of 2-[125I]iodomelatonin is rapid, stable, saturable, and reversible. Saturation studies demonstrated that 2-[125I]iodomelatonin binds to a single class of sites with an affinity constant (Kd) of 3.3 +/- 0.5 nM and a total binding capacity (Bmax) of 110.2 +/- 13.4 fmol/mg protein (n = 4). The Kd value determined from kinetic analysis (3.1 +/- 0.9 nM; n = 5) was very similar to that obtained from saturation experiments. Competition experiments showed that the relative order of potency of a variety of indoles for inhibition of 2-[125I]iodomelatonin binding site to hamster brain membranes was as follows: 6-chloromelatonin greater than or equal to 2-iodomelatonin greater than N-acetylserotonin greater than or equal to 6-methoxymelatonin greater than or equal to melatonin greater than 6-hydroxymelatonin greater than or equal to 6,7-dichloro-2-methylmelatonin greater than 5-methoxytryptophol greater than 5-methoxytryptamine greater than or equal to 5-methoxy-N,N-dimethyltryptamine greater than N-acetyltryptamine greater than serotonin greater than 5-methoxyindole (inactive). Compounds known to act at serotonergic, adrenergic, or dopaminergic receptors were either inactive or relatively ineffective as compared to melatonin. These results suggest that 2-[125I]iodomelatonin is a selective, high affinity probe for identifying melatonin receptor binding sites in rodent brain.

Effects of Timed Melatonin Infusions on Reproductive Development in the Djungarian Hamster (Phodopus sungorus)

Abstract: In confirmation of earlier work, daily melatonin infusions of 9- or 12-h duration inhibited testicular development in pinealectomized juvenile Djungarian hamsters, while daily infusions of 6-h duration did not prevent gonadal growth. Two other methoxyindoles (5-methoxytryptophol and 5-methoxytryptamine) had less than 4% of the activity shown by melatonin. When pinealectomized hamsters received two short duration (i.e. 3, 5, or 6 h) melatonin infusions each day, gonadal development was not inhibited if the two daily infusions were separated by a period of 2 or 3 h without melatonin treatment. Thus, the effects of separate pulses of melatonin were not additive in this paradigm. When single, short duration daily infusions of melatonin (5-h) or isoproterenol (6-h) were administered to pineal-intact hamsters, gonadal inhibition occurred only when the infusions were given at times that would lead to an expected overlap with and extension of the endogenous nocturnal melatonin peak. Significant inhibition of test...