Sastry B S, Phillis J W
Eur J Pharmacol. 1976 Aug;38(2):269-73. doi: 10.1016/0014-2999(76)90329-0.
Histamine (H) and H1 agonists 2-pyridylethylamine (PEA) and 2-methylhistamine (2-MH) produced a greater depression of the corticospinal and unidentified rat cerebral cortical neurones than did 4-methylhistamine (4-MH), an H2 agonist. Mepyramine antagonized the effects of 2-MH, PEA and H, and partially antagonized the depression induced by 4-MH. Metiamide and cimetidine, H2 antagonists, blocked 4-MH and H but not 2-MH- and PEA-induced depression. These results indicate that H-induced depression of cortical neurones involves activation of H1 and H2 receptors.
组胺(H)以及H1激动剂2-吡啶乙胺(PEA)和2-甲基组胺(2-MH)对大鼠皮质脊髓和未鉴定的大脑皮质神经元产生的抑制作用,比H2激动剂4-甲基组胺(4-MH)更强。美吡拉敏可拮抗2-MH、PEA和H的作用,并部分拮抗4-MH诱导的抑制作用。H2拮抗剂甲硫米特和西咪替丁可阻断4-MH和H的作用,但不能阻断2-MH和PEA诱导的抑制作用。这些结果表明,H诱导的皮质神经元抑制涉及H1和H2受体的激活。