Division of Medical Physiology, Department of Biomedical Sciences, Faculty of Health Sciences, University of Stellenbosch, Tygerberg, Cape Town, South Africa.
Physiol Res. 2011;60(2):291-301. doi: 10.33549/physiolres.931999. Epub 2010 Nov 29.
Obesity is increasing at an alarming rate globally. Several studies have shown that premenopausal women have a reduced risk of CV disease and a reduced myocardial susceptibility to ischemia/reperfusion injury. The effect of obesity on myocardial tolerance to ischemia in women has not been established. To determine how obesity affects myocardial susceptibility to ischemia/reperfusion injury in both males and females, we fed male and female Wistar rats a high caloric diet (HCD) or a control rat chow diet (CD) for 18 weeks. Rats were subsequently fasted overnight, anesthetized and blood was collected. In separate experiments, 18-week-fed (HCD and CD) rats underwent 45 min in vivo coronary artery ligation (CAL) followed by 2 hours reperfusion. Hearts were stained with TTC and infarct size determined. Both male and female HCD fed rats had increased body and visceral fat weights. Homeostasis model assessment (HOMA) index values were 13.95+/-3.04 for CD and 33.58+/-9.39 for HCD male rats (p<0.01) and 2.98+/-0.64 for CD and 2.99+/-0.72 for HCD fed female rats. Male HCD fed rats had larger infarct sizes than CD fed littermates (43.2+/-9.3 % vs. 24.4+/-7.6 %, p<0.05). Female HCD and CD diet fed rats had comparable infarct sizes (31.8+/-4.3 % vs. 23.9+/-3.3 %). We conclude that male rats on the HCD became viscerally obese, dyslipidemic and insulin-resistant, while female HCD fed rats became viscerally obese without developing dyslipidemia or insulin resistance. Obesity increased myocardial infarct size in males but not the females.
肥胖在全球范围内以惊人的速度增长。多项研究表明,绝经前女性患心血管疾病的风险降低,心肌对缺血/再灌注损伤的敏感性降低。肥胖对女性心肌对缺血的耐受性的影响尚未确定。为了确定肥胖如何影响男性和女性的心肌对缺血/再灌注损伤的耐受性,我们用高热量饮食(HCD)或对照大鼠饲料(CD)喂养雄性和雌性 Wistar 大鼠 18 周。然后,大鼠禁食过夜,麻醉并采集血液。在单独的实验中,18 周喂养的(HCD 和 CD)大鼠进行了 45 分钟的体内冠状动脉结扎(CAL),随后进行 2 小时的再灌注。心脏用 TTC 染色,并确定梗死面积。雄性和雌性 HCD 喂养的大鼠体重和内脏脂肪重量均增加。稳态模型评估(HOMA)指数值分别为 CD 喂养大鼠的 13.95+/-3.04 和 HCD 喂养大鼠的 33.58+/-9.39(p<0.01),以及 CD 喂养大鼠的 2.98+/-0.64 和 HCD 喂养大鼠的 2.99+/-0.72。HCD 喂养的雄性大鼠的梗死面积大于 CD 喂养的同窝大鼠(43.2+/-9.3%对 24.4+/-7.6%,p<0.05)。HCD 和 CD 饮食喂养的雌性大鼠的梗死面积相当(31.8+/-4.3%对 23.9+/-3.3%)。我们得出结论,高热量饮食喂养的雄性大鼠变得内脏肥胖、血脂异常和胰岛素抵抗,而高热量饮食喂养的雌性大鼠变得内脏肥胖,但没有出现血脂异常或胰岛素抵抗。肥胖增加了雄性大鼠的心肌梗死面积,但对雌性大鼠没有影响。