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首页> 外文期刊>Journal of pineal research >Therapeutic effects of melatonin on peritonitis-induced septic shock with multiple organ dysfunction syndrome in rats.
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Therapeutic effects of melatonin on peritonitis-induced septic shock with multiple organ dysfunction syndrome in rats.

机译:褪黑素对腹膜炎诱发的多器官功能不全综合征大鼠感染性休克的治疗作用。

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摘要

The pathogenesis of multiple organ dysfunction syndrome (MODS) in septic shock is complicated and not fully understood. Some studies show that an overproduction of nitric oxide (NO) leads to the refractory hypotension and multiple organ failure, while other studies suggest that free radicals, e.g. superoxide (O(2)(-)), contribute to the detrimental effect on vascular responsiveness and tissue/organ damage. Thus, this study was performed on the Wistar rat by using cecal ligation and puncture (CLP) to induce septic shock-associated MODS. We evaluated the effect of an antioxidant melatonin in CLP-induced septic rats and demonstrated that melatonin (3 mg/kg, i.v. at 3, 6, 12 hr after CLP) significantly (a) attenuated hyporeactivity to norepinephrine and delayed hypotension, (b) reduced plasma index of hepatic and renal dysfunction, (c) diminished plasma NO and interleukin-1beta (IL-1beta) concentrations as well as aortic O(2)(-) levels, (d) reduced marked infiltration of polymorphonuclear neutrophils (PMNs) in the lung and liver tissues, and (e) promoted the survival rate at 18 hr to twofold compared with the CLP alone group. The current study underlined the inhibition of plasma NO and IL-1beta as well as aortic O(2)(-) production and the reduction of PMN infiltration may lead to the amelioration of MODS, which may contribute to the beneficial effect of antioxidants (e.g. melatonin in this study) in conscious rats with peritonitis-induced lethality. Thus, the antioxidant could be a novel agent for the treatment of septic animals or patients in the early stage.
机译:败血性休克中的多器官功能障碍综合症(MODS)的发病机制很复杂,尚未完全了解。一些研究表明一氧化氮(NO)的过量产生会导致难治性低血压和多器官功能衰竭,而其他研究则表明自由基,例如超氧化物(O(2)(-)),有助于对血管反应性和组织/器官损伤的有害作用。因此,这项研究是通过盲肠结扎和穿刺(CLP)诱导败血性休克相关MODS在Wistar大鼠上进行的。我们评估了抗氧化剂褪黑激素在CLP诱导的脓毒性大鼠中的作用,并证明褪黑激素(3 mg / kg,在CLP后3、6、12 hr静脉注射)显着(a)减弱了对去甲肾上腺素的反应性降低和低血压,(b)降低肝和肾功能不全的血浆指数,(c)降低血浆NO和白介素1beta(IL-1beta)浓度以及主动脉O(2)(-)水平,(d)减少多形核中性粒细胞(PMN)的显着浸润(e)将CHR组的18小时生存率提高了两倍。当前的研究强调血浆NO和IL-1β的抑制以及主动脉O(2)(-)的产生和PMN渗透的减少可能导致MODS的改善,这可能有助于抗氧化剂的有益作用(例如褪黑素在这项研究中)在患有腹膜炎致死的清醒大鼠中。因此,抗氧化剂可能是早期治疗败血性动物或患者的新型药物。

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