地西泮对缺血再灌注大鼠肥厚心脏功能的影响

IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS International Cardiovascular Research Journal Pub Date : 2016-06-01 DOI:10.17795/ICRJ-10(2)89
D. Shackebaei, F. Feizollahi, M. Hesari, G. Bahrami
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引用次数: 3

摘要

背景:肥大的心脏易发生缺血性损伤。此外,心脏易损可以在安定存在下改变。目的:探讨地西泮对缺血再灌注条件下肥厚大鼠心脏的影响。材料与方法:雄性Wistar大鼠(体重210 ~ 270 g)单用异丙肾上腺素(4 mg/kg体重,腹腔注射7 d)或联合地西泮(1、5 mg/kg体重,腹腔注射5 d)。对照组大鼠腹腔注射生理盐水。按照langendorff法分离动物心脏,分别进行基线、缺血和再灌注阶段。然后测量心脏质量指数(心脏重量与体重之比)。心脏功能参数,包括左心室发育压和心率压产物,也在基线和缺血后进行评估。数据采用方差分析,P < 0.05为差异有统计学意义。结果:两种剂量地西泮均未达到对照组,但均能显著减轻异丙肾上腺素引起的心肌肥厚(P < 0.05)。然而,与对照组相比,地西泮(1和5 mg/kg)没有改变异丙肾上腺素诱导的加重的缺血再灌注损伤(P分别= 0.001和P = 0.013)。结论:地西泮对异丙肾上腺素引起的心肌肥厚有一定的预防作用。这种作用可能与氧化应激的改变和细胞内钙浓度的保持有关。考虑到地西泮在临床上的普遍应用,作为外周苯二氮卓类药物的配体,建议在临床试验中研究地西泮的抗肥厚作用。
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The Effect of Diazepam on the Function of Hypertrophied Rats’ Hearts in Ischemia-Reperfusion Conditions
Background : Hypertrophied hearts are susceptible to ischemic injury. Besides, cardiac vulnerability could be changed in the presence of diazepam. Objectives : The current study aimed to investigate the effect of diazepam on hypertrophied rats’ hearts in ischemia-reperfusion conditions. Materials and Methods : Male Wistar rats (body weight 210 - 270 gr) were administered with isoproterenol (4 mg/kg body weight, intraperitoneally for 7 days) alone or along with diazepam (1 and 5 mg/kg body weight, intraperitoneally for 5 days). The control rats received normal saline intraperitoneally. The animal s’ hearts were isolated according to langendorff setup and were passed through baseline, ischemia, and reperfusion stages. Then, cardiac mass index (ratio of heart weight to body weight) was measured. Cardiac functional parameters, including left ventricular developed pressure and rate pressure product, were also assessed at baseline and following ischemia. The data were analyzed using ANOVA and P < 0.05 was considered to be statistically significant. Results : Isoproterenol-induced cardiac hypertrophy was significantly reduced by both doses of diazepam compared to the group only treated with isoproterenol (P < 0.05) although it did not reach the control level. However, diazepam administration (1 and 5 mg/kg) did not change isoproterenol-induced exacerbated ischemia-reperfusion injury compared to the control group (P = 0.001 and P = 0.013, respectively). Conclusions : Diazepam relatively prevented the isoproterenol–induced cardiac hypertrophy in the animal model. This effect could be probably explained by the modification of oxidative stress and preservation of intracellular calcium concentration. Considering the common clinical usage of diazepam, as a peripheral benzodiazepine ligand, antihypertrophic effects of diazepam are recommended to be investigated in clinical trials.
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来源期刊
International Cardiovascular Research Journal
International Cardiovascular Research Journal CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
0.40
自引率
50.00%
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0
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