# HYPOTHALAMIC AMENORRHEA--NEUROENDOCRINE CHARACTERIZATION

> **NIH NIH R01** · UNIVERSITY OF CALIFORNIA, SAN DIEGO · 1994 · $168,852

## Abstract

The rapid increase in popularity of physical exercise during past
decades has led to the recognition of both beneficial and deleterious
effects.  In particular, the negative impacts of strenuous exercise on
reproductive function in women, as a consequence of centrally mediated
attenuations of GnRH/LH, pulsatile activities has become a common
clinical problem.  The management of these patients is complicated by
the presence of confounding variables such as the type and intensity
of exercise, body composition, psychologic background, and stress
factors.  In the past few years, in well controlled studies, an array
of neuroendocrine-metabolic aberrations have been identified in women
with functional  hypothalamic amenorrhea associated with vigorous
exercise and athleticism.  These include changes in virtually all
pituitary hormones and their target hormones as well as melatonin
secretion.  Although new insights with respect to the impact of chronic
vigorous exercise on multitude of hormonal changes have emerged, the
underlying mechanism(s) and their pathophysiological implications
remain to be defined.  The broad goal of this proposal is the
continuation of our efforts in delineating the underlying mechanism(s)
to account for these alterations in women with vigorous exercise, both
cycling and amenorrheic.  Experiments are designed to address five
specific aims:  i) that the recovery from reduced GnRH/LH pulsatility
in women with exercise-associated amenorrhea is manifested by a
sequence of GnRH/LH pulse patterns resembling that of a "miniature
puberty"; and that an altered FSH circadian rhythm in athletic women
with relatively normal patterns of LH pulses may be instrumental in the
development of ovarian acyclicity; ii) that the development of
hypercortisolemia in women athletes is mediated by increased
hypothalamic CRF secondary to alpha-adrenergic activation.  Increased
CRF drive may account for the activation of ACTH and cortisol
secretion, and the inhibition of the GnRH pulse generator; iii) that
the "global" reduction of circulating thyroid hormones in the presence
of a normal circadian rhythm of TSH in exercise-associated amenorrhea
may be related to diminished hypothalamic TRH secretion and/or changes
in intrapituitary Type II 5' deiodinase; iv) that the striking increase
in nocturnal melatonin secretion that occurs only in amenorrheic
athletes may reflect a dysynchronization with external cues and be
causally related to changes in alpha or beta adrenergic input,
photosensitivity, or a response to hypothyroidemia; and v) that
hypoinsulinemia and its inverse relationship to augmented IGFBP-1
levels with a consequent reduction in the bioavailability of free IGF-
1, together with hypothyroidemia, may provide a protective mechanism
in response to cellular nutritional deficits.  These studies will
include the use of antagonists and enzymatic blockers, the
characterization of pulsatile and circadian rhythmicities, nocturnal
light exposures, and anal...

## Key facts

- **NIH application ID:** 2198177
- **Project number:** 5R01HD021198-07
- **Recipient organization:** UNIVERSITY OF CALIFORNIA, SAN DIEGO
- **SAM.gov UEI:** UYTTZT6G9DT1
- **Principal Investigator:** SAMUEL S YEN
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 1994
- **Award amount:** $168,852
- **Award type:** 5
- **Project period:** 1985-12-01 → 1998-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/2198177

## Citation

> US National Institutes of Health, RePORTER application 2198177, HYPOTHALAMIC AMENORRHEA--NEUROENDOCRINE CHARACTERIZATION (5R01HD021198-07). Retrieved via MORVS 2026-10-25 from https://api.morvs.ai/grant/nih/2198177. Licensed CC0.

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