| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Endocrinology, Vol 122, 1094-1102, Copyright © 1988 by Endocrine Society
ARTICLES |
K Tsutsui, S Kawashima, A Masuda and T Oishi
Zoological Institute, Faculty of Science, Hiroshima University, Japan.
The effects of artificial photoperiod and temperature on testicular FSH binding and plasma FSH levels were studied in adult male Djungarian hamsters. In Exp I, hamsters were transferred to long day (LD) photoperiods (16-h light, 8-h dark) after 8 weeks of adaptation in short day (SD) photoperiods (8-h light, 16-h dark), but the ambient temperature was maintained at 25 C throughout the experiments. A marked increase in the total FSH binding per two testes occurred between 10 and 47 days after transfer to LD, a change that was accompanied by testicular growth. Binding of FSH per testicular weight decreased during the same period. Scatchard plot analyses of the parameters indicated that LD decreased both the concentration of FSH binding sites and the equilibrium dissociation constant (Kd). Plasma FSH levels increased between 10 and 47 days after transfer to LD. In contrast, when hamsters reared under LD for 12 weeks were transferred to SD (Exp II), FSH binding per unit weight basis increased 19 weeks after transfer to SD, but the total binding per two testes decreased markedly. In Exp III, sexually mature male hamsters were subjected to different ambient temperature and photoperiods. There were no significant effects of different ambient temperatures on the testicular weight and testicular FSH binding in animals exposed for 8 weeks to either LD or SD. However, plasma FSH levels of hamsters maintained at 25 C under LD was significantly higher than FSH levels at 7 C under LD. A similar effect of temperature on plasma FSH levels was observed in hamsters under SD. The present study indicates that photoperiod is a more important environmental factor than temperature for the regulation of FSH receptor in the Djungarian hamster.
This article has been cited by other articles:
![]() |
T. Ubuka, K. Ukena, P. J. Sharp, G. E. Bentley, and K. Tsutsui Gonadotropin-Inhibitory Hormone Inhibits Gonadal Development and Maintenance by Decreasing Gonadotropin Synthesis and Release in Male Quail Endocrinology, March 1, 2006; 147(3): 1187 - 1194. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Larkin, J. Jones, and I. Zucker Temperature dependence of gonadal regression in Syrian hamsters exposed to short day lengths Am J Physiol Regulatory Integrative Comp Physiol, March 1, 2002; 282(3): R744 - R752. [Abstract] [Full Text] [PDF] |
||||
![]() |
L.A. Howell-Skalla, D. Bunick, R.A. Nelson, and J.M. Bahr Testicular Recrudescence in the Male Black Bear (Ursus americanus): Changes in Testicular Luteinizing Hormone-, Follicle-Stimulating Hormone-, and Prolactin-Receptor Ribonucleic Acid Abundance and Dependency on Prolactin Biol Reprod, August 1, 2000; 63(2): 440 - 447. [Abstract] [Full Text] |
||||
![]() |
D. J. Bernard, I. Y. Merzlyak, T. H. Horton, and F. W. Turek Differential Regulation of Pituitary Gonadotropin Subunit Messenger Ribonucleic Acid Levels in Photostimulated Siberian Hamsters Biol Reprod, January 1, 2000; 62(1): 155 - 161. [Abstract] [Full Text] |
||||
![]() |
K. Tsutsui, D. Li, K. Ukena, M. Kikuchi, and S. Ishii Developmental Changes in Galanin Receptors in the Quail Oviduct and the Effect of Ovarian Sex Steroids on Galanin Receptor Induction Endocrinology, October 1, 1998; 139(10): 4230 - 4236. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Simoni, J. Gromoll, and E. Nieschlag The Follicle-Stimulating Hormone Receptor: Biochemistry, Molecular Biology, Physiology, and Pathophysiology Endocr. Rev., December 1, 1997; 18(6): 739 - 773. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |