The Use of Flufenamate and Forskolin to Evaluate the Role of cAMP in Gonadotropin-Releasing Hormone-Stimulated Luteinizing Hormone Secretion from Pituitaries of Ovariectomized Rats
Author:
Publisher
Wiley
Subject
Health, Toxicology and Mutagenesis,Pharmacology,Toxicology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0773.1992.tb00569.x/fullpdf
Reference26 articles.
1. Characterization of LH responses to continuous infusions of GnRH using perifused pituitaries from intact, ovariectominzed and steroid-treated rats;Baldwin;Biol. Reprod.,1983
2. Cyclic AMP indirectly mediates the extracellular Ca++-independent release of LH;Bourne;Mol. Cell. Endocrinol.,1988
3. Forskolin but not cholera toxin bypasses flufenamate-induced inhibition of cAMP production in anterior pituitaries;Bourne;Pharmacology & Toxicology,1992
4. Extracellular Ca++-independent and -dependent components of the biphasic release of LH in response to luteinizing hormone-releasing hormone in vitro;Bourne;Endocrinology,1980
5. Evidence for cAMP as a mediator of gonadotropin secretion from female pituitaries;Bourne;Amer. J. Physiol.,1987
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1. Forskolin and derivatives as tools for studying the role of cAMP;PHARMAZIE;2012
2. Effect of cAMP on GnRH stimulated LH secretion from individual pituitary gonadotropes;Molecular and Cellular Endocrinology;1995-10-30
3. Mechanism of melatonin signal transduction in the neonatal rat pituitary;Neurochemistry International;1995-09
4. Melatonin inhibition of GnRH-induced LH release from neonatal rat gonadotroph: involvement of Ca2+ not cAMP;American Journal of Physiology-Endocrinology and Metabolism;1995-07-01
5. Adenosine 3′,5′-cyclic monophosphate and the self-priming effect of gonadotrophin-releasing hormone;Molecular and Cellular Endocrinology;1995-01
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