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首页> 外文期刊>Pharmacological research: The official journal of The Italian Pharmacological Society >VERIFICATION OF PROTECTOR EFFECT OF THE NOREPINEPHRINE AND FELYPRESSIN UPON THE CARDIOVASCULAR SYSTEM UNDER ACTION OF THE LIDOCAINE HYDROCHLORIDE AND PRILOCAINE HYDROCHLORIDE IN ANESTHETIZED RATS.
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VERIFICATION OF PROTECTOR EFFECT OF THE NOREPINEPHRINE AND FELYPRESSIN UPON THE CARDIOVASCULAR SYSTEM UNDER ACTION OF THE LIDOCAINE HYDROCHLORIDE AND PRILOCAINE HYDROCHLORIDE IN ANESTHETIZED RATS.

机译:盐酸利多卡因和盐酸普利卡因在大鼠体内的作用下,验证去甲肾上腺素和草叶加压素对心血管系统的保护作用。

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Vasoconstrictor substances, as norepinephrine and epinephrine, were mixtured to local anesthetics to decrease their toxic effects and to prolong the depth of the anesthesia. However, these catecholamines produce systolic and diastolic hypertension. The effects of felypressin, a synthetic vasoconstrictor, upon arterial blood pressure and heart are lesser than those of norepinephrine or epinephrine, but due to its effects like oxytocin these catecholamines are yet the most used vasoconstrictors in association with lidocaine or another anesthetic salt. These vasoconstrictors are contraindicated for some physician, mainly for cardiac patients. But, are the catecholamines or is the salt the most dangerous components of the local anesthetic? The effects of the salt and catecholamines are opposite, but which of these exercises their effects first when inside blood vessel? Singi et al. [Pharmacol. Res. 44 (2001)] demonstrated that the first effect is always of the salt and that norepinephrine promotes protector effects upon guinea-pig isolated heart against lidocaine action. But, is this true for in vivo animals? The present study was performed with the aiming to answer this question and to verify if felypressin can induce the same effect of the norepinephrine. Fourteen Rattus norvegicus albinus, weighing 350g on average, were used. After being anesthetized with sodic thiopental, they were tracheostomizeds and one jugular and one carotid were cannuled for application of substances and to record the blood arterial pressure, respectively. The ECG was gotten through electrodes located in the front and back paws of the animals. The animals were separated in two groups, each one with seven rats. The lidocaine hydrochloride 2% in the doses of 600&mgr;g and 3% in the doses of 900&mgr;g acted on the cardiovascular system reducing the arterial pressure and modifying the electrocardiogram, while the prilocaine hydrochloride, in the same doses, also reduced the arterial pressure, but did not modify the electrocardiogram. When norepinephrine was associated to lidocaine 3% hydrochloride, it was possible to observe that this salt always exercised its effect first and a protective effect against the fall of pressure produced for the lidocaine. The same protective effect did not occur when felypressin was associated with prilocaine hydrochloride 3%.
机译:将去甲肾上腺素和肾上腺素等血管收缩物质混合到局部麻醉剂中以降低其毒性作用并延长麻醉深度。但是,这些儿茶酚胺会产生收缩期和舒张期高血压。非加压素(一种合成的血管收缩药)对动脉血压和心脏的作用要小于去甲肾上腺素或肾上腺素,但由于它们的作用像催产素一样,这些儿茶酚胺仍然是与利多卡因或另一种麻醉盐结合使用最多的血管收缩药。这些血管收缩剂对某些医生是禁忌的,主要是对心脏病患者。但是,儿茶酚胺或盐是局部麻醉药中最危险的成分吗?盐和儿茶酚胺的作用是相反的,但是在血管内时,这些盐和儿茶酚胺中的哪一种首先发挥作用? Singi等。 [Pharmacol。 Res。 [44(2001)]证明了第一个作用始终是盐,去甲肾上腺素对豚鼠离体心脏促进了利多卡因作用的保护作用。但是,对于体内动物而言,这是真的吗?进行本研究的目的是回答这个问题,并验证飞凌加压素是否可以诱导去甲肾上腺素的相同作用。使用了十四只褐家鼠,平均重350克。用钠硫喷妥钠麻醉后,将它们气管切开,分别给一个颈静脉和一个颈动脉插管以施用物质并记录血压。心电图是通过位于动物前后爪上的电极获得的。将动物分成两组,每组七只大鼠。盐酸利多卡因2mg(600mg / g)和3%(900mgg)对心血管系统起作用,降低了动脉压并改变了心电图,而盐酸丙胺卡因(相同剂量)也降低了动脉压力,但未修改心电图。当去甲肾上腺素与3%的利多卡因盐酸盐结合时,可以观察到该盐始终首先发挥其作用,并且对利多卡因产生的压力下降具有保护作用。当felypressin与3%盐酸丙胺卡因联合使用时,未发生相同的保护作用。

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