Akella Aparna, Tiwari Anil K, Patne Shashikant C U, Deshpande Shripad B
Department of Physiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, India.
Department of Physiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, India.
Toxicon. 2015 Apr;97:15-22. doi: 10.1016/j.toxicon.2015.02.004. Epub 2015 Feb 7.
The present study was undertaken to determine whether acute respiratory distress syndrome (ARDS) is produced after Mesobuthus tamulus (MBT) envenomation and compared it with oleic acid (OA)-induced ARDS. The trachea, jugular vein and femoral artery were cannulated in anesthetized adult rats. Lethal dose of MBT venom (5 mg/kg) or OA (75 μL) was administered intravenously and the time-dependent changes in respiratory frequency (RF), heart rate (HR) and mean arterial pressure (MAP) were recorded. Minute ventilation (MV) and the PaO2/FiO2 (P/F) ratio were also determined. At the end lungs were excised, one lung was used for histopathological examination and the other was used for determination of pulmonary water content physically. MBT venom or OA produced hypoxemia, pulmonary pathology (alveolar damage, infiltration of inflammatory cells, capillary damage and exudation) and pulmonary edema implicating for ARDS. However, the hypoxemia in MBT venom group was associated with decreased MV, apnea/bradypnea, and bradycardia whereas, in OA group it was seen with increased MV, tachypnea, and tachycardia. Lack of effect of hypoxemic drive on RF/MV or HR in MBT venom group unlike OA group, suggests the involvement of medullary centers. The present results demonstrate that MBT venom produces ARDS. However MBT venom-induced ARDS involves pulmonary as well as extrapulmonary mechanisms.
本研究旨在确定中华眼镜蛇(MBT)毒液注射后是否会引发急性呼吸窘迫综合征(ARDS),并将其与油酸(OA)诱导的ARDS进行比较。在麻醉的成年大鼠中插入气管、颈静脉和股动脉。静脉注射致死剂量的MBT毒液(5mg/kg)或OA(75μL),并记录呼吸频率(RF)、心率(HR)和平均动脉压(MAP)随时间的变化。还测定了分钟通气量(MV)和动脉血氧分压/吸入氧分数值(P/F)。实验结束时切除肺脏,一个肺用于组织病理学检查,另一个用于物理测定肺含水量。MBT毒液或OA可导致低氧血症、肺部病变(肺泡损伤、炎性细胞浸润、毛细血管损伤和渗出)以及肺水肿,提示发生了ARDS。然而,MBT毒液组的低氧血症与MV降低、呼吸暂停/呼吸过缓以及心动过缓有关,而在OA组中,低氧血症则与MV增加、呼吸急促和心动过速有关。与OA组不同,MBT毒液组低氧驱动对RF/MV或HR无影响,提示髓质中心参与其中。目前的结果表明,MBT毒液可引发ARDS。然而,MBT毒液诱导的ARDS涉及肺内和肺外机制。