Chang Ching-Ping, Chen Sheng-Hsien, Lin Mao-Tsun
Department of Biotechnology, Southern Taiwan University of Technology, Tainan, Taiwan 710.
Shock. 2005 Oct;24(4):336-40. doi: 10.1097/01.shk.0000175894.18168.66.
We assess the effects of ipsapirone (a 5-HT1A receptor agonist), ketanserin (a 5-HT2A receptor antagonist), (-)-pindolol (a 5-HT1A receptor antagonist), and DOI (a 5-HT2A receptor agonist) on heatstroke in a rat model. Animals, under urethane anesthesia, were exposed to high ambient temperature of 42 degrees C until mean arterial pressure and local cerebral blood flow in the striatum began to decrease, which was arbitrarily defined as the onset of heatstroke. Normothermic controls were exposed to room temperature of 24 degrees C. In rats treated with normal saline immediately before the initiation of heat stress, the values for survival time were found to be 21 to 25 min. Systemic administration of ipsapirone (10 mg/kg) or ketanserin (2 mg/kg) immediately before the initiation of heat stress significantly increased the survival time to new values of 92 to 104 min. Combined treatment with ipsapirone and ketanserin had additive effects (survival time of 156-194 min). In contrast, systemic administration of (-)-pindolol (2 mg/kg) or DOI (2 mg/kg) significantly decreased the survival time to new values of 2 to 3 min. In vehicle-treated heatstroke rats, the values for core temperature, intracranial pressure, and the extracellular levels of cellular ischemia (e.g., glutamate and lactate/pyruvate ratio) or damage (e.g., glycerol) markers and neuronal damage scores in striatum were significantly higher than those of normothermic controls. On the other hand, the values for mean arterial pressure, cerebral perfusion pressure, cerebral blood flow, and brain partial pressure of O2 were significantly lower than those of normothermic controls. The heatstroke-induced hyperthermia, arterial hypotension, intracranial hypertension, cerebral hypoperfusion and hypoxia, and increased levels of cellular ischemia and damage markers in striatum were all significantly attenuated by prior administration of ipsapirone or ketanserin. The present results strongly suggest that previous activation of 5-HT1A receptors or antagonism of 5-HT2A receptors protects against heatstroke by reducing circulatory shock and cerebral ischemia, whereas prior antagonism of 5-HT1A receptors or activation of 5-HT2A receptors exacerbates heatstroke.
我们评估了ipsapirone(一种5-HT1A受体激动剂)、酮色林(一种5-HT2A受体拮抗剂)、(-)-吲哚洛尔(一种5-HT1A受体拮抗剂)和DOI(一种5-HT2A受体激动剂)对大鼠热射病模型的影响。在乌拉坦麻醉下,将动物暴露于42℃的高环境温度下,直到平均动脉压和纹状体局部脑血流量开始下降,这被任意定义为热射病的发作。正常体温对照组暴露于24℃的室温下。在热应激开始前立即用生理盐水处理的大鼠中,存活时间为21至25分钟。在热应激开始前立即全身给予ipsapirone(10mg/kg)或酮色林(2mg/kg)可显著延长存活时间,新的存活时间为92至104分钟。ipsapirone和酮色林联合治疗具有相加作用(存活时间为156 - 194分钟)。相比之下,全身给予(-)-吲哚洛尔(2mg/kg)或DOI(2mg/kg)可显著缩短存活时间,新的存活时间为2至3分钟。在给予赋形剂处理的热射病大鼠中,核心温度、颅内压以及纹状体中细胞缺血(如谷氨酸和乳酸/丙酮酸比值)或损伤(如甘油)标志物的细胞外水平和神经元损伤评分显著高于正常体温对照组。另一方面,平均动脉压、脑灌注压、脑血流量和脑氧分压的值显著低于正常体温对照组。ipsapirone或酮色林预先给药可显著减轻热射病诱导的体温过高、动脉低血压、颅内高压、脑灌注不足和缺氧以及纹状体中细胞缺血和损伤标志物水平的升高。目前的结果强烈表明,先前激活5-HT1A受体或拮抗5-HT2A受体可通过减少循环性休克和脑缺血来预防热射病,而先前拮抗5-HT1A受体或激活5-HT2A受体则会加重热射病。