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丙泊酚可减轻过氧化氢诱导的离体大鼠心脏机械和代谢紊乱。

Propofol attenuates hydrogen peroxide-induced mechanical and metabolic derangements in the isolated rat heart.

作者信息

Kokita N, Hara A

机构信息

Department of Anesthesiology, Sapporo Medical University School of Medicine, Japan.

出版信息

Anesthesiology. 1996 Jan;84(1):117-27. doi: 10.1097/00000542-199601000-00014.

Abstract

BACKGROUND

Oxygen-derived free radicals are involved in tissue damage during myocardial ischemia and reperfusion. Recent in vitro studies have demonstrated that a beneficial effect of propofol lies on its free radical scavenging properties. The current study, therefore, examined whether propofol is effective against the mechanical and metabolic damage induced by exogenously administered hydrogen peroxide in the isolated rat heart.

METHODS

Rat hearts were perfused aerobically with Krebs-Henseleit bicarbonate buffer at a constant flow rate according to Langendorff's technique, while being paced electrically. Hearts were studied in control Krebs-Henseleit bicarbonate buffer, with Intralipid vehicle, with 25 microM or 50 microM propofol for 40 min, and with 50 microM propofol for 30 min followed by Intralipid for 10 min. A similar set of hearts was treated with hydrogen peroxide for 4 min, either in the absence of or beginning 10 min after Intralipid or propofol infusion. Left ventricular pressure was recorded as an index of mechanical function. The tissue concentrations of adenosine triphosphate, adenosine diphosphate, adenosine monophosphate, and creatine phosphate were measured as indices of energy metabolism. The tissue concentration of malondialdehyde was measured to evaluate lipid peroxidation.

RESULTS

Hydrogen peroxide (600 microM) significantly increased the left ventricular end-diastolic pressure, decreased the left ventricular developed pressure (i.e., it produced mechanical dysfunction), and decreased tissue concentrations of adenosine triphosphate and creatine phosphate (i.e., metabolic damage). Hydrogen peroxide also increased the tissue concentration of malondialdehyde. These mechanical and metabolic alterations induced by hydrogen peroxide were significantly attenuated by propofol (25 microM or 50 microM), while the increase in malondialdehyde was completely suppressed by propofol.

CONCLUSIONS

The current study demonstrates that in the isolated heart, propofol attenuates both mechanical and metabolic changes induced by exogenously applied hydrogen peroxide. The beneficial action of propofol is probably correlated with reduction of the hydrogen peroxide-induced lipid peroxidation.

摘要

背景

氧衍生的自由基参与心肌缺血和再灌注期间的组织损伤。最近的体外研究表明,丙泊酚的有益作用在于其自由基清除特性。因此,本研究检测了丙泊酚对外源性过氧化氢诱导的离体大鼠心脏机械和代谢损伤是否有效。

方法

根据Langendorff技术,以恒定流速用Krebs-Henseleit碳酸氢盐缓冲液对大鼠心脏进行有氧灌注,同时进行电起搏。在对照Krebs-Henseleit碳酸氢盐缓冲液、含脂质乳剂载体、含25微摩尔或50微摩尔丙泊酚的情况下对心脏进行40分钟的研究,以及在含50微摩尔丙泊酚的情况下进行30分钟的研究,随后含脂质乳剂10分钟。另一组相似的心脏在脂质乳剂或丙泊酚输注前或输注开始10分钟后,用过氧化氢处理4分钟。记录左心室压力作为机械功能指标。测量三磷酸腺苷、二磷酸腺苷、一磷酸腺苷和磷酸肌酸的组织浓度作为能量代谢指标。测量丙二醛的组织浓度以评估脂质过氧化。

结果

过氧化氢(600微摩尔)显著增加左心室舒张末期压力,降低左心室发展压力(即产生机械功能障碍),并降低三磷酸腺苷和磷酸肌酸的组织浓度(即代谢损伤)。过氧化氢还增加丙二醛的组织浓度。丙泊酚(25微摩尔或50微摩尔)显著减轻过氧化氢诱导的这些机械和代谢改变,而丙泊酚完全抑制丙二醛的增加。

结论

本研究表明,在离体心脏中,丙泊酚减轻外源性过氧化氢诱导的机械和代谢变化。丙泊酚的有益作用可能与减少过氧化氢诱导的脂质过氧化有关。

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