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脂质体抗氧化剂对大鼠脑缺血再灌注损伤的防治作用

Liposomal antioxidants in combating ischemia-reperfusion injury in rat brain.

作者信息

Sinha J, Das N, Basu M K

机构信息

Biomembrane Division, Indian Institute of Chemical Biology, Calcutta, India.

出版信息

Biomed Pharmacother. 2001 Jun;55(5):264-71. doi: 10.1016/s0753-3322(01)00060-9.

Abstract

Liposome-encapsulated antioxidants have been tested in vivo to prevent oxidative attack during cerebral ischemia and reperfusion. Oxidative stress is a causal factor in the neuropathogenesis of ischemic-reperfusion injury. From the therapeutic point of view free chemical antioxidants were almost ineffective to protect cerebral tissues from those oxidative attacks. Thus an attempt has been made to prevent the oxidative damage due to the cerebral ischemic insult by the introduction of chemical antioxidants, ascorbic acid and alpha-tocopherol either encapsulated or intercalated in small unilamellar liposomes. The effectiveness of antioxidant-loaded liposomes was tested against an experimental in vivo rat model of global cerebral ischemia. Oxidative free radical attack on cerebral tissues by the ischemic insult and brief reperfusion was accounted for by the amount of diene production per unit of tissue protein. Diene production in ischemic reperfused rat brain increases almost twofold over that of the normal rats. Prevention of excess diene production has been attributed to rats when they were treated either with L-ascorbic acid-encapsulated liposomes or alpha-tocopherol intercalated liposomes 2 hours prior to the cerebral ischemic insult. Complete restriction of excess diene generation has also been achieved when a mixture of alpha-tocopherol and L-ascorbic acid-encapsulated liposomes were injected 3 hours before the ischemic infraction.

摘要

脂质体包裹的抗氧化剂已在体内进行测试,以预防脑缺血和再灌注期间的氧化攻击。氧化应激是缺血再灌注损伤神经发病机制中的一个致病因素。从治疗角度来看,游离化学抗氧化剂几乎无法有效保护脑组织免受这些氧化攻击。因此,人们尝试通过引入化学抗氧化剂(如包裹或嵌入小单层脂质体中的抗坏血酸和α-生育酚)来预防因脑缺血损伤引起的氧化损伤。针对整体脑缺血的实验性体内大鼠模型测试了负载抗氧化剂的脂质体的有效性。缺血损伤和短暂再灌注对脑组织的氧化自由基攻击通过每单位组织蛋白的二烯生成量来衡量。缺血再灌注大鼠脑内的二烯生成量比正常大鼠增加了近两倍。当在脑缺血损伤前2小时用包裹L-抗坏血酸的脂质体或嵌入α-生育酚的脂质体治疗大鼠时,已将二烯生成过量的预防归因于这些脂质体。当在缺血性梗死前3小时注射α-生育酚和包裹L-抗坏血酸的脂质体混合物时,也实现了对过量二烯生成的完全抑制。

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