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Neuroendocrine effects of sumatriptan.

作者信息

Herdman J R, Delva N J, Hockney R E, Campling G M, Cowen P J

机构信息

MRC Unit of Clinical Pharmacology, Littlemore Hospital, Oxford, UK.

出版信息

Psychopharmacology (Berl). 1994 Jan;113(3-4):561-4. doi: 10.1007/BF02245240.

DOI:10.1007/BF02245240
PMID:7862876
Abstract

The neuroendocrine effects of the 5-HT receptor agonist, sumatriptan (6 mg subcutaneously), were studied in 11 healthy male subjects using a placebo-controlled, cross-over design. Compared to placebo, sumatriptan significantly lowered levels of plasma prolactin but increased those of plasma growth hormone. There was no effect on plasma cortisol concentrations. The neuroendocrine effects of sumatriptan differ from those of previously described 5-HT-receptor agonists, and may be a consequence of selective activation of 5-HT1D or 5-HT1B receptors. However, the present data cannot exclude the possibility that the neuroendocrine changes reflect nonspecific stress responses or changes in pituitary blood flow.

摘要

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皮下注射舒马曲坦对偏头痛患者的神经内分泌影响。
J Endocrinol Invest. 2001 May;24(5):310-4. doi: 10.1007/BF03343866.
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MK-212 increases rat plasma ACTH concentration by activation of the 5-HT1C receptor subtype.MK-212 通过激活 5-羟色胺 1C 受体亚型来提高大鼠血浆促肾上腺皮质激素(ACTH)浓度。
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Sumatriptan (GR 43175) interacts selectively with 5-HT1B and 5-HT1D binding sites.舒马曲坦(GR 43175)选择性地与5-HT1B和5-HT1D结合位点相互作用。
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Neuropharmacology. 1990 Jun;29(6):511-3. doi: 10.1016/0028-3908(90)90061-u.