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首页> 外文期刊>Toxicology mechanisms and methods >Reevaluation of arrhythmias and alterations of the autonomic nervous activity induced by T-2 toxin through telemetric measurements in unrestrained rats.
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Reevaluation of arrhythmias and alterations of the autonomic nervous activity induced by T-2 toxin through telemetric measurements in unrestrained rats.

机译:重新评估心律不齐和T-2毒素诱导的自主神经活动的变化,通过遥测法在不受约束的大鼠中进行。

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摘要

This study was conducted to clarify and reevaluate the cardiac and autonomic nervous effects of T-2 toxin, which had been previously examined by several acute experiments, in unrestrained and conscious rats implanted with telemetric transmitters. Two groups of rats were given two subcutaneous injections of 0.1 and 0.5?mg/kg of T-2 toxin with an interval of 3 days. Two other groups of rat were pre-implanted with osmotic minipumps by which atropine (20?mg/kg/day) or propranolol (100?mg/kg/day) was continuously administered preceding subcutaneous injection of T-2 toxin (0.5?mg/kg). The present study demonstrated that T-2 toxin caused marked arrhythmias, such as second-degree atrioventricular (AV) block, sinus bradycardia, supraventricular extrasystole, and ventricular extrasystole, which were accompanied by a significant increase in heart rate and a significant decrease in total power and low- and high-frequency power of heart rate variability, during 3 days of observation after the toxin administration. However, the occurrence of arrhythmia with conduction disturbance such as second-degree atrioventricular blocks was markedly diminished by pretreatment with atropine, while the occurrence of ventricular extrasystole was augmented by atropine. The present study with the telemetric measurement elucidated and confirmed that T-2 toxin produced significant cardiac dysfunctions involving disturbance of the conduction pathway influenced by the autonomic nervous activity and also possible direct effects on cardiac myocytes.
机译:进行这项研究的目的是阐明和重新评估T-2毒素对心脏和自主神经的影响,该作用先前已通过几次急性实验在植入遥测发射器的不受约束的清醒大鼠中进行了检验。两组大鼠分别皮下注射0.1和0.5?mg / kg的T-2毒素,间隔3天。另两组大鼠预先植入了渗透微泵,在皮下注射T-2毒素(0.5?mg)之前,连续服用阿托品(20?mg / kg /天)或普萘洛尔(100?mg / kg /天)。 /公斤)。本研究表明,T-2毒素可引起明显的心律失常,例如二级房室传导阻滞,窦性心动过缓,室上性早搏和室性早搏,并伴有心率的显着增加和总心律的明显降低。毒素给药后3天的观察期间,心率变异性的功率和低频和高频功率。但是,阿托品预处理可显着减少传导障碍(如二级房室传导阻滞)引起的心律不齐的发生,而阿托品可增加心室收缩期的发生。通过遥测技术进行的本研究阐明并证实,T-2毒素产生了严重的心脏功能障碍,涉及受自主神经活动影响的传导途径的干扰,还可能对心肌细胞产生直接影响。

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