Literature DB >> 1110345

Exogenous and endogenous control of the annual reproductive cycle in the male golden hamster: participation of the pineal gland.

R J Reiter.   

Abstract

Testes and accessory sex organs (seminal vesicles and coagulating glands) of hamsters exposed to natural lighting (NL) conditions beginning September 22 underwent complete degeneration by October 31. The following February the testes began to regrow with the regeneration being complete by mid to late March. Associated with the atrophic response of the testes during the winter months was consistent depression in pituitary prolactin and an inconsistent decrease in pituitary luteinizing hormone levels. If hamsters are pineal lectomized prior to their exposure to NL, the sexual organs do not atrophy and the pituitary hormone levels do not drop. Moving hamsters from NL to the long daily photoperiods (light:dark cycles of 14 hrs light and 10 hrs darknessLD 14:10) of the laboratory near mid winter is followed by regrowth of the gonads and accessory glands. Regeneration of the reproductive system in the spring is not a function of increasing photoperiodic length since if animals are completely deprived of light (by blinding) in February, the gonads still regenerate. When hamsters are exposed to LD 14:10 cycles during the subsequent summer, the return to NL on September 22 is followed by a second involution of the reproductive system. However, if the period of LD 14:10 (the simulated summer) is shortened by ten weeks, the second return to NL does not initiate involution of the reproductive system. During the simulated summer complete light deprivation by blinding is incapable of forcing atrophy of the sexual organs.

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Year:  1975        PMID: 1110345     DOI: 10.1002/jez.1401910111

Source DB:  PubMed          Journal:  J Exp Zool        ISSN: 0022-104X


  15 in total

1.  The pineal gland and seasonal reproductive adjustments.

Authors:  R J Reiter
Journal:  Int J Biometeorol       Date:  1975-12       Impact factor: 3.787

2.  The pineal gland of the mole (Talpa europaea L.) III. A fluorescence histochemical study.

Authors:  P Pevet; M T Juillard; A R Smith; J A Kappers
Journal:  Cell Tissue Res       Date:  1976-01-27       Impact factor: 5.249

3.  The pineal gland of the mole-rat (Spalax ehrenbergi, Nehring). I. The fine structure of pinealocytes.

Authors:  P Pevet; J A Kappers; E Nevo
Journal:  Cell Tissue Res       Date:  1976-10-22       Impact factor: 5.249

4.  Seasonal changes in the uptake capacity of the suprachiasmatic nucleus for 3H-serotonin.

Authors:  D C Meyer; W B Quay
Journal:  Experientia       Date:  1977-04-15

5.  Elimination of testicular regression by 12-hr temporal relationship of serotonergic and dopaminergic activity in Indian palm squirrel, Funambulus pennanti.

Authors:  R Jaiwal; C M Chaturvedi
Journal:  J Neural Transm Gen Sect       Date:  1991

Review 6.  The ultrastructure of pinealocytes in the golden mole (Amblysomus hottentotus) with special reference to the granular vesicles.

Authors:  P Pevet; M A Kuyper
Journal:  Cell Tissue Res       Date:  1978-07-13       Impact factor: 5.249

7.  Circadian variation in urinary melatonin in clinically healthy women in Japan and the United States of America.

Authors:  L Wetterberg; F Halberg; B Tarquini; M Cagnoni; E Haus; K Griffith; T Kawasaki; L A Wallach; M Ueno; K Uezo; M Matsuoka; M Kuzel; E Halberg; T Omae
Journal:  Experientia       Date:  1979-03-15

8.  Pineal melatonin synthesis in Syrian hamsters: a summary.

Authors:  M D Rollag
Journal:  Int J Biometeorol       Date:  1982-12       Impact factor: 3.787

9.  Photoperiod: its importance as an impeller of pineal and seasonal reproductive rhythms.

Authors:  R J Reiter
Journal:  Int J Biometeorol       Date:  1980-03       Impact factor: 3.787

10.  The pineal gland of nocturnal mammals. II. The ultrastructure of the pineal gland in the pipistrelle bat (Pipistrellus pipistrellus L.): presence of two populations of pinealocytes.

Authors:  P Pévet; P A Racey
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

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