Literature DB >> 10567862

Evidence that neuronal nitric oxide synthase but not heme oxygenase increases in the hypothalamus on proestrus afternoon.

C A Lamar1, G K Bhat, V B Mahesh, D W Brann.   

Abstract

Nitric oxide (NO) has been implicated in the control of the proestrus luteinizing hormone (LH) surge in the rat but to date no studies have attempted to measure neuronal nitric oxide synthase (nNOS) or NO production on proestrus in the hypothalamus in order to determine if endogenous NO is increased on proestrus afternoon to activate gonadotropin-releasing hormone (GnRH) neurons. To address this deficit in our knowledge, we measured nNOS mRNA and protein levels as well as NOS activity levels in rat preoptic area (POA) and medial basal hypothalamus (MBH) fragments at 12.00, 14.00, 16.00, and 18.00 h of proestrus. Serum LH levels were also assessed to determine whether NOS changes correlate to the LH surge. To determine the specificity of observed changes we also measured mRNA levels for the enzyme heme oxygenase-2, which is responsible for production of another putative gaseous transmitter, carbon monoxide. In all studies a metestrus 12.00 h control group was included since steroid and LH levels would be basal at this time as compared to proestrus. The results revealed that nNOS mRNA and protein levels, as well as NOS activity did not change significantly in the MBH on proestrus. In contrast, nNOS mRNA levels were significantly elevated in the POA at proestrus 12.00 and 14.00 h, as compared to metestrus 12.00 h. Likewise, at the protein and activity level, nNOS protein levels in the POA were significantly elevated on proestrus at 14.00 and 16.00 h, with NOS activity significantly increased at 16.00 h on proestrus. The elevation of nNOS protein and activity levels in the POA occurred at the time of initiation of the LH surge. The elevation of nNOS was specific as mRNA levels for the CO-synthetic enzyme heme oxygenase-2 did not change significantly on proestrus in the POA or MBH. As a whole, the current studies provide new evidence that nNOS is elevated in the POA on proestrus, and thus could play a role in the activation of GnRH neurons to produce the preovulatory LH surge. Copyright 1999 S. Karger AG, Basel.

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Year:  1999        PMID: 10567862     DOI: 10.1159/000054497

Source DB:  PubMed          Journal:  Neuroendocrinology        ISSN: 0028-3835            Impact factor:   4.914


  5 in total

1.  Preoptic neuronal nitric oxide synthase induction by testosterone is consistent with a role in gating male copulatory behavior.

Authors:  Nicholas S R Sanderson; Brandon Le; Zifei Zhou; David Crews
Journal:  Eur J Neurosci       Date:  2008-01       Impact factor: 3.386

2.  Phosphorylation of N-methyl-D-aspartic acid receptor-associated neuronal nitric oxide synthase depends on estrogens and modulates hypothalamic nitric oxide production during the ovarian cycle.

Authors:  Jyoti Parkash; Xavier d'Anglemont de Tassigny; Nicole Bellefontaine; Celine Campagne; Danièle Mazure; Valérie Buée-Scherrer; Vincent Prevot
Journal:  Endocrinology       Date:  2010-04-06       Impact factor: 4.736

Review 3.  Hirsutism, virilism, polycystic ovarian disease, and the steroid-gonadotropin-feedback system: a career retrospective.

Authors:  Virendra B Mahesh
Journal:  Am J Physiol Endocrinol Metab       Date:  2011-10-25       Impact factor: 4.310

4.  Estradiol induces physical association of neuronal nitric oxide synthase with NMDA receptor and promotes nitric oxide formation via estrogen receptor activation in primary neuronal cultures.

Authors:  Xavier d'Anglemont de Tassigny; Céline Campagne; Sophie Steculorum; Vincent Prevot
Journal:  J Neurochem       Date:  2009-02-02       Impact factor: 5.372

5.  Estradiol and progesterone modulate the nitric oxide/cyclic gmp pathway in the hypothalamus of female rats and in GT1-1 cells.

Authors:  Hsiao-Pai Chu; Gayatri Sarkar; Anne M Etgen
Journal:  Endocrine       Date:  2004-07       Impact factor: 3.633

  5 in total

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