Institut Für Pharmakologie und Toxikologie, Medizinische Fakultät, Martin-Luther-Universität Halle-Wittenberg, 06097, Halle, Germany.
Medizinische Fakultät, Herzchirurgie, Martin-Luther-Universität Halle-Wittenberg, 06097, Halle, Germany.
Naunyn Schmiedebergs Arch Pharmacol. 2023 Sep;396(9):2137-2150. doi: 10.1007/s00210-023-02457-x. Epub 2023 Mar 23.
We investigated whether hypothermia and hyperthermia can alter the efficacy and potency of histamine at increasing the force of cardiac contractions in mice that overexpress the human H receptor only in their cardiac myocytes (labelled H-TG). Contractile studies were performed in an organ bath on isolated, electrically driven (1 Hz) left atrial preparations and spontaneously beating right atrial preparations from H-TG mice and wild-type (WT) littermate control mice. The basal beating rate in the right atrial preparations from H-TG mice was lowered by hypothermia (23 °C) and elevated by hyperthermia (42 °C). Furthermore, the efficacy of histamine (0.01-100 µM) at exerting positive inotropic effects was more severely attenuated in the left and right H-TG mouse atria under hypothermia and hyperthermia than under normothermia (37 °C). Similarly, the inotropic response to histamine was attenuated under hypothermia and hyperthermia in isolated electrically stimulated (1 Hz) right atrial preparations obtained from humans undergoing cardiac surgery. The phosphorylation state of phospholamban at serine 16 at 23 °C was inferior to that at 37 °C in left atrial preparations from H-TG mice in the presence of 10 µM histamine. In contrast, in human atrial preparations, the phosphorylation state of phospholamban at serine 16 in the presence of 100 µM histamine was lower at 42 °C than at 37 °C. Finally, under hyperthermia, we recorded more and longer lasting arrhythmias in right atrial preparations from H-TG mice than in those from WT mice. We conclude that the inotropic effects of histamine in H-TG mice and in human atrial preparations, as well as the chronotropic effects of histamine in H-TG mice, are temperature dependent. Furthermore, we observed that, even without stimulation of the H receptors by exogenous agonists, temperature elevation can increase arrhythmias in isolated right atrial preparations from H-TG mice. We propose that H receptors play a role in hyperthermia-induced supraventricular arrhythmias in human patients.
我们研究了在仅在心肌细胞中过表达人 H 受体的小鼠(标记为 H-TG)中,低温和高温是否会改变组胺增加心肌收缩力的效力和效价。在离体、电驱动(1 Hz)左心房标本和自发跳动的右心房标本上进行收缩研究,这些标本来自 H-TG 小鼠和野生型(WT)同窝对照小鼠。H-TG 小鼠右心房标本的基础跳动率在低温(23°C)下降低,在高温(42°C)下升高。此外,在低温和高温下,H-TG 小鼠左、右心房中组胺(0.01-100 μM)发挥正性变力作用的效力比在正常体温(37°C)下更严重减弱。同样,在低温和高温下,在接受心脏手术的人类离体电刺激(1 Hz)右心房标本中,组胺的变力反应也减弱。在存在 10 μM 组胺的情况下,H-TG 小鼠左心房标本中磷酸化酶蛋白 at 丝氨酸 16 的磷酸化状态在 23°C 下不如在 37°C 下好。相比之下,在人类心房标本中,在存在 100 μM 组胺的情况下,磷酸化酶蛋白 at 丝氨酸 16 的磷酸化状态在 42°C 下低于 37°C。最后,在高温下,我们记录到 H-TG 小鼠右心房标本中的心律失常比 WT 小鼠多且持续时间更长。我们得出结论,H-TG 小鼠和人类心房标本中组胺的变力作用以及 H-TG 小鼠中组胺的变时作用都依赖于温度。此外,我们观察到,即使没有外源性激动剂刺激 H 受体,温度升高也会增加 H-TG 小鼠离体右心房标本中的心律失常。我们提出 H 受体在人类患者中高温诱导的室上性心律失常中起作用。