Levi R, Malm J R, Bowman F O, Rosen M R
Circ Res. 1981 Aug;49(2):545-50. doi: 10.1161/01.res.49.2.545.
We used standard microelectrode techniques to study the effects of histamine on right atrial tissues from patients undergoing corrective cardiac surgery. In the 10(-6) to 10(-4) M range, histamine increased maximum diastolic potential, action potential amplitude, and automaticity. In some preparations, histamine also induced delayed afterdepolarizations and triggered activity. The potency of histamine in increasing automaticity was about 10 times less than that of epinephrine. Propranolol (2 x 10(-7)M), which abolished the chronotropic effect of epinephrine, did not alter the effect of histamine. Conversely, the effect of histamine but not that of epinephrine was antagonized by cimetidine (3 x 10(-6) to 1 x 10(-5) M). This suggests that H2 receptors mediate the chronotropic effects of histamine on the human heart. The slow channel blocker verapamil (2 x 10(-8) to 2 x 10(-6) M) counteracted the effects of histamine on automaticity, delayed afterdepolarizations, and triggered activity, suggesting that in human atrium histamine may act by increasing slow inward (presumably Ca2+) current. If one considers these arrhythmogenic effects of histamine and the fact that human cardiac tissue contains large amounts of histamine, our experiments lend further support to the concept that histamine release can induce arrhythmias.
我们采用标准微电极技术,研究组胺对接受心脏矫正手术患者右心房组织的影响。在10⁻⁶至10⁻⁴M范围内,组胺可增加最大舒张电位、动作电位幅度及自律性。在一些标本中,组胺还可诱发延迟后去极化及触发活动。组胺增加自律性的效能约为肾上腺素的十分之一。普萘洛尔(2×10⁻⁷M)可消除肾上腺素的变时作用,但不改变组胺的作用。相反,西咪替丁(3×10⁻⁶至1×10⁻⁵M)可拮抗组胺的作用,但不影响肾上腺素的作用。这表明H₂受体介导组胺对人心脏的变时作用。慢通道阻滞剂维拉帕米(2×10⁻⁸至2×10⁻⁶M)可抵消组胺对自律性、延迟后去极化及触发活动的影响,提示在人心房中组胺可能通过增加慢内向(可能是Ca²⁺)电流起作用。如果考虑到组胺的这些致心律失常作用以及人心脏组织中含有大量组胺这一事实,我们的实验进一步支持了组胺释放可诱发心律失常这一概念。