Pourkhalili Khalil, Fatemikia Hossein, Kim Euikyung, Mashayekhy Navid Reza, Dounighi Naser Mohammadpour, Hajivandi Abdollah, Hassan Yaghoob, Seyedian Ramin
Department of Physiology, Faculty of Medicine, Bushehr University of Medical Sciences, Bushehr, Iran.
Department of Physiology, Faculty of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
J Arthropod Borne Dis. 2018 Mar 18;12(1):31-40. eCollection 2018 Mar.
We investigated the hemodynamic changes (Inotropic, chronotropic and arrhythmogenic) in intravenously envenomed anesthetized rats with venom. The neutralizing potencies of different drugs and commercial antivenom were assessed simultaneously.
Different doses of the crude venom (100, 200 and 400μg/rat) were injected during five minutes via the femoral vein and cardiovascular changes were recorded in rats in Razi Institute Corporation, Karaj, Iran in 2017. The drugs (Atropine, lidocaine, propranolol and prazosin) were injected before the venom for determination of the counteracting effects. Different volumes (100, 500 and 1000μl) of the antivenom were pre envenomed to neutralize cardiovascular changes.
Temporary hypertension and bradycardia with no arrhythmogenic effects were depicted within twenty minutes. There was a difference in arterial pressure between the venom (400μg/rat) and the vehicle at 8 minutes (114.68±5.1mmHg versus 70.2±4.3mmHg). Elevation of the mean arterial pressure was inhibited by propranolol (2 mg/kg) and neutralized by prazosin (1mg/kg) while lidocaine (4mg/kg) and atropine (1mg/kg) had no effects. Premedication with Iranian commercial antivenom (1000μl) produced surprisingly temporary hypertension compared to the vehicle (140.84±4.5 versus 84.3±3.2). It had no neutralizing properties on blood pressure variation before the venom injection. Volume-expanded hypertension phenomenon was ruled out in a parallel study.
This venom has vasoconstrictive effects in rats probably due to the presence of norepinephrine like materials in its content or liberated from adrenal gland inhibited by prazosin premedication. The neutralizing effects of antivenom on venom-induced hypertension are questionable.
我们研究了静脉注射毒液的麻醉大鼠的血流动力学变化(变力性、变时性和致心律失常性)。同时评估了不同药物和商业抗蛇毒血清的中和效力。
2017年在伊朗卡拉季的拉齐研究所公司,通过股静脉在五分钟内注射不同剂量的粗毒液(100、200和400μg/大鼠),并记录大鼠的心血管变化。在注射毒液前注射药物(阿托品、利多卡因、普萘洛尔和哌唑嗪)以确定其对抗作用。预先注射不同体积(100、500和1000μl)的抗蛇毒血清以中和心血管变化。
二十分钟内出现短暂性高血压和心动过缓,无致心律失常作用。在8分钟时,毒液(400μg/大鼠)和赋形剂之间的动脉压存在差异(114.68±5.1mmHg对70.2±4.3mmHg)。普萘洛尔(2mg/kg)抑制平均动脉压升高,哌唑嗪(1mg/kg)中和,而利多卡因(4mg/kg)和阿托品(1mg/kg)无作用。与赋形剂相比,预先注射伊朗商业抗蛇毒血清(1000μl)产生了令人惊讶的短暂性高血压(140.84±4.5对84.3±3.2)。它在注射毒液前对血压变化没有中和作用。在一项平行研究中排除了容量扩张性高血压现象。
这种毒液在大鼠中具有血管收缩作用,可能是由于其成分中存在去甲肾上腺素样物质或由哌唑嗪预处理抑制的肾上腺释放的物质。抗蛇毒血清对毒液诱导的高血压的中和作用值得怀疑。