help button home button Endocrine Society Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schreihofer, D. A.
Right arrow Articles by Cameron, J. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schreihofer, D. A.
Right arrow Articles by Cameron, J. L.

Endocrinology, Vol 132, 1881-1889, Copyright © 1993 by Endocrine Society


ARTICLES

Suppression of luteinizing hormone secretion during short-term fasting in male rhesus monkeys: the role of metabolic versus stress signals

DA Schreihofer, DB Parfitt and JL Cameron
Department of Behavioral Neuroscience, University of Pittsburgh, Pennsylvania 15260.

One day of fasting leads to a significant suppression of pulsatile LH secretion in adult male rhesus monkeys that is evident within the first 4-6 h after a missed meal. Restricting food intake may suppress the central drive to the reproductive axis via metabolic signals occurring during the transition from a fed, energy storing state to a fasted, energy mobilizing state or via signals associated with the "psychological stress" imposed by withholding food. To distinguish between these two general types of signals, we chose the experimental strategy of providing monkeys with a great excess of calories on the day before fasting (i.e. overfeeding on the day before fasting) in order to maintain them in a metabolically fed state on the following day when they were fasted, without preventing the psychological stress associated with fasting. We reasoned that if metabolic signals are responsible for causing the fasting-induced suppression of LH secretion, overfeeding on the day before fasting would prevent the fasting-induced suppression of LH secretion. Eight adult male rhesus monkeys with indwelling venous catheters were studied on three occasions: on a day of normal feeding (receiving approximately 30 pellets of monkey chow at 1100 h on the day of the study), on a day of fasting after a day of normal feeding, and on a day of fasting after a day of overfeeding (receiving one meal of 100 pellets on the day before the study). Pulsatile LH secretion on a day of fasting after a day of normal feeding (0.4 +/- 0.2 pulses/6 h, measured from 1200-1800 h) was significantly suppressed, P < 0.05, compared to a day of normal feeding (1.8 +/- 0.3 pulses/6 h). In contrast, on a day of fasting after a day of overfeeding there was no significant difference in LH secretion measured from 1200-1800 h (1.5 +/- 0.3 pulses/6 h) compared to a day of normal feeding. Overfeeding the day before fasting prevented the normal fasting-induced suppression of plasma T3 concentrations and delayed the normal fasting-induced decline in plasma insulin concentrations. Overfeeding did not prevent the display of agitated behavior that we have previously documented in monkeys when they are fasted. These results support the hypothesis that the signal(s) which suppresses normal LH secretion after brief periods of fasting is related to the metabolic status of the body during the transition from a fed to a fasted state, rather than a function of the psychological state imposed by withholding food.


This article has been cited by other articles:


Home page
EndocrinologyHome page
M. E. Lujan, A. A. Krzemien, R. L. Reid, and D. A. Van Vugt
Developing a Model of Nutritional Amenorrhea in Rhesus Monkeys
Endocrinology, January 1, 2006; 147(1): 483 - 492.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
S. M. Moenter and R. A. DeFazio
Endogenous {gamma}-Aminobutyric Acid Can Excite Gonadotropin-Releasing Hormone Neurons
Endocrinology, December 1, 2005; 146(12): 5374 - 5379.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
Z. Chu and S. M. Moenter
Endogenous Activation of Metabotropic Glutamate Receptors Modulates GABAergic Transmission to Gonadotropin-Releasing Hormone Neurons and Alters Their Firing Rate: A Possible Local Feedback Circuit
J. Neurosci., June 15, 2005; 25(24): 5740 - 5749.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
N. R. Vulliemoz, E. Xiao, L. Xia-Zhang, S. L. Wardlaw, and M. Ferin
Central Infusion of Agouti-Related Peptide Suppresses Pulsatile Luteinizing Hormone Release in the Ovariectomized Rhesus Monkey
Endocrinology, February 1, 2005; 146(2): 784 - 789.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
G. N. Wade and J. E. Jones
Neuroendocrinology of nutritional infertility
Am J Physiol Regulatory Integrative Comp Physiol, December 1, 2004; 287(6): R1277 - R1296.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
A.-S. Parent, G. Teilmann, A. Juul, N. E. Skakkebaek, J. Toppari, and J.-P. Bourguignon
The Timing of Normal Puberty and the Age Limits of Sexual Precocity: Variations around the World, Secular Trends, and Changes after Migration
Endocr. Rev., October 1, 2003; 24(5): 668 - 693.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
J. Lado-Abeal, J. D. Veldhuis, and R. L. Norman
Glucose Relays Information Regarding Nutritional Status to the Neural Circuits That Control the Somatotropic, Corticotropic, and Gonadotropic Axes in Adult Male Rhesus Macaques
Endocrinology, February 1, 2002; 143(2): 403 - 410.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
N. I. Williams, D. L. Helmreich, D. B. Parfitt, A. Caston-Balderrama, and J. L. Cameron
Evidence for a Causal Role of Low Energy Availability in the Induction of Menstrual Cycle Disturbances during Strenuous Exercise Training
J. Clin. Endocrinol. Metab., November 1, 2001; 86(11): 5184 - 5193.
[Abstract] [Full Text] [PDF]


Home page
Arch Gen PsychiatryHome page
E. A. Young, A. R. Midgley, N. E. Carlson, and M. B. Brown
Alteration in the Hypothalamic-Pituitary-Ovarian Axis in Depressed Women
Arch Gen Psychiatry, December 1, 2000; 57(12): 1157 - 1162.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
K. J. Suter, W. J. Song, T. L. Sampson, J.-P. Wuarin, J. T. Saunders, F. E. Dudek, and S. M. Moenter
Genetic Targeting of Green Fluorescent Protein to Gonadotropin-Releasing Hormone Neurons: Characterization of Whole-Cell Electrophysiological Properties and Morphology
Endocrinology, January 1, 2000; 141(1): 412 - 419.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
M. P. Warren, F. Voussoughian, E. B. Geer, E. P. Hyle, C. L. Adberg, and R. H. Ramos
Functional Hypothalamic Amenorrhea: Hypoleptinemia and Disordered Eating
J. Clin. Endocrinol. Metab., March 1, 1999; 84(3): 873 - 877.
[Abstract] [Full Text]


Home page
Biol. Reprod.Home page
D.L. Foster and S. Nagatani
Physiological Perspectives on Leptin as a Regulator of Reproduction: Role in Timing Puberty
Biol Reprod, February 1, 1999; 60(2): 205 - 215.
[Abstract] [Full Text] [PDF]




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
Copyright © 1993 by The Endocrine Society