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首页> 外文期刊>Regulatory Toxicology and Pharmacology: RTP >Subchronic safety evaluation of CMS-1 (a botanical antihypertensive product derived from Semen Cnidium monnieri) in Sprague-Dawley rats and beagle dogs
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Subchronic safety evaluation of CMS-1 (a botanical antihypertensive product derived from Semen Cnidium monnieri) in Sprague-Dawley rats and beagle dogs

机译:CMS-1(一种源自精子念珠菌的植物降压产品)在Sprague-Dawley大鼠和beagle犬中的亚慢性安全性评估

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摘要

CMS-1, mainly composed of imperatorin as its active compound, is a partially purified fraction of a Chinese herbal medicine, Semen Cnidium monnieri. CMS-1 has the potential to be further developed as a new treatment for hypertension. Thus, we studied its toxicity in both Sprague-Dawley rats and beagle dogs. Rats (0-900. mg/kg/day) and dogs (0-450. mg/kg/day) received CMS-1 orally for 30 consecutive days, followed by a 15-day recovery period. The major target organs of CMS-1 toxicity are the GI (inappetence), liver (hepatocellular necrosis, enzyme elevation), thymus (atrophy), cardiovascular (hypotension), changes in ECG T and P waveforms, elevation of nitrous oxide levels and hematological (RBC parameters disturbances) systems. Most treatment-induced adverse effects were reversible or showed a progressive recovery upon discontinuation of the treatment. The No Observed Adverse Effect Level (NOAEL) was 100. mg/kg/day for rats and 50. mg/kg/day for dogs. This non-clinical study suggests that clinical monitoring of CMS-1 in patients should focus on the gastrointestinal system, blood tests for liver functions, electrolytes, and blood homeostasis, cardiovascular functions, and immune functions.
机译:CMS-1主要由欧前胡素为有效成分,是中草药精子猴头草的部分纯化成分。 CMS-1有可能被进一步开发为高血压的新疗法。因此,我们研究了它对Sprague-Dawley大鼠和beagle狗的毒性。大鼠(0-900。mg / kg /天)和狗(0-450。mg / kg /天)连续30天口服CMS-1,然后恢复15天。 CMS-1毒性的主要靶器官是GI(食欲不振),肝脏(肝细胞坏死,酶升高),胸腺(萎缩),心血管(低血压),ECG T和P波形变化,一氧化二氮水平升高和血液学(RBC参数扰动)系统。大多数治疗引起的不良反应是可逆的,或在治疗中止后逐渐恢复。大鼠的未观察到不良反应水平(NOAEL)为100. mg / kg /天,狗为50. mg / kg /天。这项非临床研究表明,对患者CMS-1的临床监测应集中在胃肠道系统,肝功能,电解质和血液稳态,血液功能,心血管功能和免疫功能的血液检查。

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