Schmidt G, Ahrén K, Brännström M, Kannisto P, Owman C, Sjöberg N O, Tenenbaum A
Neuroendocrinology. 1987 Jun;46(1):69-74. doi: 10.1159/000124798.
The effect of histamine on progesterone synthesis and cyclic adenosine 3',5'-monophosphate (cAMP) accumulation was studied in superfused and incubated follicles dissected free from immature rats treated with pregnant mare serum gonadotrophin (PMSG). Histamine, like LH, increased the progesterone synthesis, but to a smaller extent. The H2-antagonist, cimetidine, inhibited completely the histamine-induced progesterone increase while the H1-antagonist, pyrilamine, as well as propranolol and atropine did not affect the initial response but modified its duration. The specific H2-agonist, 4-methylhistamine, but not the H1-agonist, 2-methylhistamine, mimicked the effect of histamine on progesterone synthesis. In the presence of the phosphodiesterase inhibitor, IBMX, histamine increased tissue levels of cAMP. These results suggest that histamine stimulates progesterone synthesis via the H2-receptor with cAMP acting as secondary intracellular messenger.
在从用孕马血清促性腺激素(PMSG)处理的未成熟大鼠中分离出的、进行了灌流和孵育的卵泡中,研究了组胺对孕酮合成和环磷酸腺苷(cAMP)积累的影响。组胺与促黄体生成素(LH)一样,能增加孕酮的合成,但程度较小。H2拮抗剂西咪替丁完全抑制了组胺诱导的孕酮增加,而H1拮抗剂吡苄明以及普萘洛尔和阿托品并不影响初始反应,但改变了其持续时间。特异性H2激动剂4-甲基组胺能模拟组胺对孕酮合成的作用,而H1激动剂2-甲基组胺则不能。在磷酸二酯酶抑制剂异丁基甲基黄嘌呤(IBMX)存在的情况下,组胺增加了组织中的cAMP水平。这些结果表明,组胺通过H2受体刺激孕酮合成,cAMP作为细胞内的第二信使发挥作用。