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一氧化氮供体对高胆固醇饮食家兔心肌损伤严重程度的改善作用。

Amelioration of severity of myocardial injury by a nitric oxide donor in rabbits fed a cholesterol-rich diet.

作者信息

Hoshida S, Nishida M, Yamashita N, Igarashi J, Hori M, Kamada T, Kuzuya T, Tada M

机构信息

Division of Cardiology, First Department of Medicine, Osaka University School of Medicine, Japan.

出版信息

J Am Coll Cardiol. 1996 Mar 15;27(4):902-9. doi: 10.1016/0735-1097(95)00538-2.

Abstract

OBJECTIVES

This study compared the effect of a nitric oxide donor on limiting the size of infarct resulting from myocardial ischemia-reperfusion between atherosclerotic and nonatherosclerotic models.

BACKGROUND

Endothelial-derived relaxation in coronary arteries affected by ischemia is substantially impaired after reperfusion, and this impairment may exacerbate the myocardial ischemia-reperfusion injury. In animals with experimental atherosclerosis, release of endothelial-derived relaxing factor is also decreased, and the propagation of myocardial infarction could be exacerbated.

METHODS

We examined the extent of myocardial injury induced by ischemia (30 min) and reperfusion (48 hr) in rabbits fed a cholesterol-rich (1%) or normal diet for 10 weeks. We also evaluated the effect of a nitric oxide donor (S-nitroso-N-acetylpenicillamine [SNAP], a nitric oxide precursor (L-arginine) or a degradation product of SNAP (N-acetylpenicillamine) on infarct size in these models.

RESULTS

Severity of myocardial injury was significantly exacerbated in cholesterol-fed rabbits (75.2 +/- 4.4% [mean +/- SEM]) compared with that in non-cholesterol-fed rabbits (53.2 +/- 5.2%). This exacerbation was prevented by treatment with SNAP (50.2 +/- 6.4%) but not with L-arginine (70.5 +/- 6.0%) or N-acetylpenicillamine (70.4 +/- 4.8%) in cholesterol-fed-rabbits. However, SNAP did not limit infarct size in non-cholesterol-fed rabbits (60.8 +/- 4.2%). The rate-pressure product was similar during the course of the experiment in all the groups.

CONCLUSIONS

Myocardial damage induced by ischemia-reperfusion was significantly exacerbated in rabbits fed a long-term cholesterol-rich diet but was effectively reversed by treatment with a nitric oxide donor. However, this agent did not limit infarct size in normal rabbits. Thus, a nitric oxide donor reduces myocardial infarct size in atherosclerotic but not in nonatherosclerotic rabbits.

摘要

目的

本研究比较了一氧化氮供体在限制动脉粥样硬化模型和非动脉粥样硬化模型中因心肌缺血再灌注所致梗死面积方面的作用。

背景

缺血影响的冠状动脉内皮源性舒张在再灌注后会严重受损,这种损伤可能会加剧心肌缺血再灌注损伤。在实验性动脉粥样硬化动物中,内皮源性舒张因子的释放也会减少,心肌梗死的扩展可能会加剧。

方法

我们检查了喂食富含胆固醇(1%)或正常饮食10周的兔子在缺血(30分钟)和再灌注(48小时)后诱导的心肌损伤程度。我们还评估了一氧化氮供体(S-亚硝基-N-乙酰青霉胺[SNAP])、一氧化氮前体(L-精氨酸)或SNAP的降解产物(N-乙酰青霉胺)对这些模型中梗死面积的影响。

结果

与未喂食胆固醇的兔子(53.2±5.2%)相比,喂食胆固醇的兔子(75.2±4.4%[平均值±标准误])心肌损伤的严重程度显著加剧。在喂食胆固醇的兔子中,用SNAP治疗(50.2±6.4%)可预防这种加剧,但用L-精氨酸(70.5±6.0%)或N-乙酰青霉胺(70.4±4.8%)则不能。然而,SNAP并没有限制未喂食胆固醇的兔子的梗死面积(60.8±4.2%)。在实验过程中,所有组的心率血压乘积相似。

结论

长期喂食富含胆固醇饮食的兔子因缺血再灌注诱导的心肌损伤显著加剧,但用一氧化氮供体治疗可有效逆转。然而,该药物并没有限制正常兔子的梗死面积。因此,一氧化氮供体可减少动脉粥样硬化兔子的心肌梗死面积,但不能减少非动脉粥样硬化兔子的心肌梗死面积。

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