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单剂量镁预防对成年Wistar大鼠异丙肾上腺素诱导的心肌梗死缺乏心脏保护作用。

Lack of cardioprotection by single-dose magnesium prophylaxis on isoprenaline-induced myocardial infarction in adult Wistar rats.

作者信息

Garson Christie, Kelly-Laubscher Roisin, Blackhurst Dee, Gwanyanya Asfree

机构信息

Department of Human Biology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Department of Clinical Laboratory Sciences, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

出版信息

Cardiovasc J Afr. 2015 Nov-Dec;26(6):242-9. doi: 10.5830/CVJA-2015-055. Epub 2015 Jul 14.

Abstract

AIM

Magnesium (Mg(2+)) is effective in treating cardiovascular disorders such as arrhythmias and pre-eclampsia, but its role during myocardial infarction (MI) remains uncertain. In this study, we investigated the effects of Mg(2+)pre-treatment on isoprenaline (ISO) -induced MI in vivo.

METHODS

Rats divided into four groups were each pre-treated with either MgSO4 (270 mg/kg intraperitoneally) or an equivalent volume of physiological saline, prior to the ISO (67 mg/kg subcutaneously) or saline treatments. One day post-treatment, the electrocardiogram and left ventricular blood pressures were recorded. Infarcts were determined using 2,3,5-triphenyltetrazolium chloride staining, and serum markers of lipid peroxidation were measured with spectrophotometric assays.

RESULTS

Mg(2+) pre-treatment neither altered the ISO-induced infarct size compared with ISO treatment alone (p > 0.05), nor reversed the low-voltage electrocardiogram or the prominent Q waves induced by ISO, despite a trend to decreased Q waves. Similarly, Mg(2+) did not prevent the ISO-induced decrease in peak left ventricular blood pressure or the decrease in minimal rate of pressure change. Mg(2+) did not reverse the ISO-induced gain in heart weight or loss of body weight. Neither ISO nor Mg(2+) altered the concentrations of lipid peroxidation markers 24 hours post MI induction.

CONCLUSION

Although Mg(2+) had no detrimental effects on electrical or haemodynamic activity in ISO-induced MI, the lack of infarct prevention may detract from its utility in MI therapy.

摘要

目的

镁离子(Mg(2+))在治疗心律失常和先兆子痫等心血管疾病方面有效,但其在心肌梗死(MI)过程中的作用仍不明确。在本研究中,我们调查了Mg(2+)预处理对异丙肾上腺素(ISO)诱导的体内心肌梗死的影响。

方法

将大鼠分为四组,在进行ISO(67 mg/kg皮下注射)或生理盐水处理之前,分别用硫酸镁(270 mg/kg腹腔注射)或等量的生理盐水进行预处理。处理后一天,记录心电图和左心室血压。使用2,3,5-三苯基氯化四氮唑染色确定梗死面积,并用分光光度法测定脂质过氧化的血清标志物。

结果

与单独的ISO处理相比,Mg(2+)预处理既未改变ISO诱导的梗死面积(p > 0.05),也未逆转ISO诱导的低电压心电图或明显的Q波,尽管有Q波减小的趋势。同样,Mg(2+)也未阻止ISO诱导的左心室血压峰值降低或压力变化最小速率的降低。Mg(2+)未逆转ISO诱导的心脏重量增加或体重减轻。在心肌梗死诱导后24小时,ISO和Mg(2+)均未改变脂质过氧化标志物的浓度。

结论

尽管Mg(2+)对ISO诱导的心肌梗死的电活动或血流动力学活动没有不利影响,但缺乏对梗死的预防作用可能会降低其在心肌梗死治疗中的效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d48c/4780018/97a6f9eea420/cvja-26-243-g001.jpg

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