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An in vivo and in vitro study: High-dosage Danshen injection induces peripheral vascular endothelial cells injury

机译:体内和体外研究:大剂量丹参注射液诱导周围血管内皮细胞损伤

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摘要

Danshen injection, a pharmaceutical dosage form of Danshen, has been widely used in the treatment of coronary heart diseases, myocardial infarction, and hypertension. With more and more adverse drug reactions linked with Danshen injection, its safety comes under suspicion. To evaluate its safety, mice were divided into four groups: vehicle, low-, middle-, and high-Danshen group, and each group was intravenously administered with Danshen injection at a dose of 0, 0.64, 1.55, and 5.76 g/kg/day for 5 days, respectively (the low dosage was the recommended clinical dosage, the middle dosage was the most commonly used higher dosage, and the high dosage was the highest dosage used in clinic). Peripheral vascular toxicity wasn't observed in the low-dosage group, elevated serum endothelin-1 (ET-1) was observed in the middle-dosage group; and more peripheral vascular toxicities like increased vascular leakage, elevated serum nitrate and ET-1, and vascular endothelial cells apoptosis were detected in the high-dosage group. In vitro study, low-concentration Danshen injection showed protective effect to human umbilical vein endothelial cells (HUVECs), while high concentration displayed strong cytotoxic effects, including increase in nitric oxide and ET-1 production, inhibition of cell viability, and apoptosis induction. Further, the HUVECs' apoptosis induced by high-concentration Danshen injection was found along with the induction of reactive oxygen species. In conclusion, these results suggest that Danshen injection is nontoxic in its recommended clinical dosage, and the 2.4-fold as the recommended clinical dosage might be the highest safety dosage in clinic treatment. In addition, Danshen injection is a potential vascular toxic drug in its high dosage and shouldn't be used far beyond its recommended dosage in clinic treatment.
机译:丹参注射液是丹参的药物剂型,已广泛用于治疗冠心病,心肌梗塞和高血压。随着越来越多的不良反应与丹参注射液相关联,其安全性受到怀疑。为了评估其安全性,将小鼠分为四组:媒介物,低,中,高丹参组,每组分别以0、0.64、1.55和5.76 g / kg的剂量静脉内注射丹参注射液/天,分别为5天(低剂量是推荐的临床剂量,中剂量是最常用的较高剂量,高剂量是临床上使用的最高剂量)。低剂量组未见周围血管毒性,中剂量组未见血清内皮素-1(ET-1)升高。高剂量组检测到更多的外周血管毒性,如血管渗漏增加,血清硝酸盐和ET-1升高以及血管内皮细胞凋亡。在体外研究中,低浓度丹参注射液显示出对人脐静脉内皮细胞(HUVEC)的保护作用,而高浓度丹参注射液则显示出强大的细胞毒性作用,包括增加一氧化氮和ET-1的产生,抑制细胞活力以及诱导细胞凋亡。此外,还发现了高浓度丹参注射液诱导的HUVECs凋亡以及活性氧的诱导。总之,这些结果表明丹参注射液在其推荐的临床剂量中是无毒的,而作为推荐临床剂量的2.4倍可能是临床治疗中最高的安全剂量。此外,丹参注射液以高剂量是一种潜在的血管毒性药物,在临床治疗中不应超过推荐剂量使用。

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