The overall goal of this continuing research is to delineate the mechanisms involved in the suppression of gonadotropin secretion induced by the suckling stimulus. All of our data is consistent with the hypothesis that suckling greatly suppresses GnRH release from the hypothalamus leading to a decrease in pituitary gonadotropin function, as evidenced by a decrease in pituitary GnRH receptors, pituitary sensitivity to GnRH, LH submit mRNA and pulsatile LH secretion. Thus, this system provides an excellent model in which to study the mechanisms involved in the restoration of normal pituitary gonadotrope function from a physiologically suppressed state. The studies proposed will also attempt to identify the factors associated with lactation that are responsible for the suppression of GnRH secretion. The proposed experiments will examine the differential regulation of LH and FSH secretion by measuring LH and FSH subunit mRNA levels during lactation and after pup removal, and also will examine the effects of administration of pulsatile GnRH and estradiol and progesterone on gonadotrophin subunit mRNA levels. Studies will determine if factors other than suppressed GnRH secretion may play a role during lactation in the decrease in pituitary GnRH receptors and pituitary sensitivity to GnRH. Studies will also more clearly define the recovery process of GnRH secretion after pup removal by characterizing the pattern of LH secretion between 0 and 24hr after pup removal and will test the hypothesis that the pattern of GnRH recovery after pup removal consists of an early increase in basal secretion, which upregulates GnRH receptors, followed later by the superimposition of GnRH pulses, which initiates pulsatile LH secretion. Techniques will be developed to measure GnRH biosynthesis by using 3H-amino acids to label newly synthesized GnRH. It is hoped that changes in GnRH biosynthesis will serve as an indicator of changes in GnRH neuronal activity. Studies will determine whether factors involved in suckling-induced prolactin and oxytocin secretion, such as VIP, oxytocin, activin, and serotonin, may also mediate the suppression of GnRH secretion. Because our experiments have shown that suppression of GnRH secretion requires input from areas of the CNS outside the hypothalamus, and neural impulses from the suckling stimulus travel through the lower brainstem to reach the hypothalamus, experiments will be conducted to identify areas in the lower brainstem which are responsible for the inhibitory input which suppress GnRH secretion. These studies should provide new insights into the regulation of GnRH secretion and pituitary gonadotrope function, and thus may contribute to new approaches for contraception, to correct infertility problems, and to an understanding of the mechanisms participating in lactation amenorrhea.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD014643-11
Application #
3312727
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1979-12-01
Project End
1994-03-31
Budget Start
1991-04-01
Budget End
1992-03-31
Support Year
11
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Type
Schools of Medicine
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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Baquero, Arian F; Kirigiti, Melissa A; Baquero, Karalee C et al. (2015) Developmental changes in synaptic distribution in arcuate nucleus neurons. J Neurosci 35:8558-69
Baquero, Arian F; de Solis, Alain J; Lindsley, Sarah R et al. (2014) Developmental switch of leptin signaling in arcuate nucleus neurons. J Neurosci 34:9982-94
Verma, Saurabh; Kirigiti, Melissa A; Millar, Robert P et al. (2014) Endogenous kisspeptin tone is a critical excitatory component of spontaneous GnRH activity and the GnRH response to NPY and CART. Neuroendocrinology 99:190-203
Lee, Shin J; Verma, Saurabh; Simonds, Stephanie E et al. (2013) Leptin stimulates neuropeptide Y and cocaine amphetamine-regulated transcript coexpressing neuronal activity in the dorsomedial hypothalamus in diet-induced obese mice. J Neurosci 33:15306-17
Lee, Shin J; Kirigiti, Melissa; Lindsley, Sarah R et al. (2013) Efferent projections of neuropeptide Y-expressing neurons of the dorsomedial hypothalamus in chronic hyperphagic models. J Comp Neurol 521:1891-914
True, Cadence; Verma, Saurabh; Grove, Kevin L et al. (2013) Cocaine- and amphetamine-regulated transcript is a potent stimulator of GnRH and kisspeptin cells and may contribute to negative energy balance-induced reproductive inhibition in females. Endocrinology 154:2821-32
Nicol, L E; Grant, W F; Grant, W R et al. (2013) Pancreatic inflammation and increased islet macrophages in insulin-resistant juvenile primates. J Endocrinol 217:207-13
True, C; Kirigiti, M A; Kievit, P et al. (2011) Leptin is not the critical signal for kisspeptin or luteinising hormone restoration during exit from negative energy balance. J Neuroendocrinol 23:1099-112
Sullivan, Elinor L; Smith, M Susan; Grove, Kevin L (2011) Perinatal exposure to high-fat diet programs energy balance, metabolism and behavior in adulthood. Neuroendocrinology 93:1-8

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