Polanin A, McNeill J H
Can J Physiol Pharmacol. 1981 Jan;59(1):19-24. doi: 10.1139/y81-004.
The effects of selective histamine receptor analogs were studied in electrically paced rabbit left atria. Atrial tension was increased by histamine (an H1 and H2 agonist), 4-methylhistamine and impromidine (H2 agonists), and 2-pyridylethylamine (PEA) (an H1 agonist). The responses to histamine and impromidine were not altered by propranolol (1 x 10(-7) M) or reserpine pretreatment. However, the responses to 4-methylhistamine and PEA were significantly decreased upon pretreatment with propranolol or reserpine. Promethazine pretreatment (H1 receptor blockade) antagonized the inotropic effects of histamine and PEA but had no effect on the responses to 4-methylhistamine or impromidine. Cimetidine pretreatment (H2 receptor antagonism) competitively blocked the positive inotropic effects of histamine, 4-methylhistamine, and impromidine. These results suggest that the left atrial inotropic response is mediated through H1 and H2 receptor stimulation.
在电刺激的兔左心房中研究了选择性组胺受体类似物的作用。组胺(一种H1和H2激动剂)、4-甲基组胺和英普咪定(H2激动剂)以及2-吡啶乙胺(PEA,一种H1激动剂)可增加心房张力。普萘洛尔(1×10⁻⁷ M)或利血平预处理不改变对组胺和英普咪定的反应。然而,用普萘洛尔或利血平预处理后,对4-甲基组胺和PEA的反应显著降低。异丙嗪预处理(H1受体阻断)拮抗组胺和PEA的正性肌力作用,但对4-甲基组胺或英普咪定的反应无影响。西咪替丁预处理(H2受体拮抗)竞争性阻断组胺、4-甲基组胺和英普咪定的正性肌力作用。这些结果表明,左心房正性肌力反应是通过H1和H2受体刺激介导的。