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血管紧张素Ⅳ类似物Dihexa对脑出血小鼠的神经保护作用及其机制
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作者 胡燕 郑晓梅 张佳丽 《山东医药》 CAS 2023年第8期38-42,共5页
目的观察血管紧张素Ⅳ类似物Dihexa对脑出血小鼠的神经保护作用,并探讨作用机制。方法将110只C57BL/6J小鼠随机分为假手术组、模型组、药物1组、药物2组、抑制剂组,每组22只。模型组、药物1组、药物2组、抑制剂组采用胶原酶法制备脑出... 目的观察血管紧张素Ⅳ类似物Dihexa对脑出血小鼠的神经保护作用,并探讨作用机制。方法将110只C57BL/6J小鼠随机分为假手术组、模型组、药物1组、药物2组、抑制剂组,每组22只。模型组、药物1组、药物2组、抑制剂组采用胶原酶法制备脑出血模型,假手术组以生理盐水代替胶原酶进行注射,其余操作与其他组一致。造模成功后,药物1组、药物2组分别予Dihexa 1.44、2.88 mg/(kg·d)灌胃,抑制剂组先后予wortmannin(PI3K选择性抑制剂)0.5 mg/(kg·d)、Dihexa 2.88 mg/(kg·d)灌胃,模型组和假手术组给予等体积生理盐水,连续3 d。给药结束后采用改良Garcia评分评估神经功能缺损情况,检测脑组织含水量,HE染色观察脑组织病理改变,ELISA法检测脑组织中的肿瘤坏死因子α(TNF-α)、白细胞介素1β(IL-1β),TUNEL法检测神经细胞凋亡情况,Western blotting法检测脑组织中的凋亡相关蛋白(cleaved-Caspase3、Bcl-2)及磷脂酰激醇-3-激酶(PI3K)/丝氨酸/苏氨酸蛋白激酶B(AKT)通路蛋白。结果与假手术组相比,模型组、药物1组、药物2组、抑制剂组的脑组织含水量、脑组织中TNF-α、IL-1β、cleaved-Caspase3表达及神经细胞凋亡率增高,神经功能评分、脑组织中Bcl-2表达及p-PI3K/PI3K、p-AKT/AKT降低(P均<0.05)。模型组、药物1组、药物2组的的脑组织含水量、脑组织中TNF-α、IL-1β、cleavedCaspase3表达及神经细胞凋亡率依次降低,神经功能评分、脑组织中Bcl-2表达及p-PI3K/PI3K、p-AKT/AKT依次增高(P均<0.05)。抑制剂组脑组织含水量、脑组织中TNF-α、IL-1β、cleaved-Caspase3表达及神经细胞凋亡率高于药物2组,神经功能评分、脑组织中Bcl-2表达及p-PI3K/PI3K、p-AKT/AKT低于药物2组(P均<0.05)。结论血管紧张素Ⅳ类似物Dihexa可以剂量依赖性减轻脑出血小鼠神经细胞凋亡和炎症反应,保护神经功能;其作用机制可能与调控PI3K-AKT通路有关。 展开更多
关键词 dihexa 血管紧张素Ⅳ类似物 脑出血 细胞凋亡 炎症反应 PI3K-AKT信号通路 动物实验
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Small molecule activation of the neurotrophin hepatocyte growth factor to treat Alzheimer disease
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作者 John W.Wright Joseph W.Harding 《Neuroimmunology and Neuroinflammation》 2021年第2期70-80,共11页
Alzheimer's disease(AD)is a neurodegenerative disease characterized by progressive neuron loses in memory-related brain structures.Five drugs have been approved by the FDA to treat Alzheimer's disease;however,... Alzheimer's disease(AD)is a neurodegenerative disease characterized by progressive neuron loses in memory-related brain structures.Five drugs have been approved by the FDA to treat Alzheimer's disease;however,these drugs have failed to modify or significantly slow disease progression.New therapies are needed to delay the course of this disease and hopefully prevent further neuron losses.This review describes available AD drugs and several novel approaches presently being investigated.We next describe relevant biomarkers and urge greater research interest in the potential utilization of neurotrophic agents to treat AD.Neurotrophins such as nerve growth factor,brain-derived neurotrophic factor and hepatocyte growth factor(HGF)are capable of stimulating dendritic arborization,synaptogenesis,stem cell differentiation,neurogenesis,and decreases in neuroinflammation,oxidative stress-induced damage and neurotoxicity due to a wide range of cellular insults.We present the strategy of utilizing small molecule analogs specifically designed to penetrate the blood-brain barrier and facilitate dimerization and activation of the HGF/Met receptor system.These molecules have been shown to encourage the formation of new functional synaptic connections,induce long-term potentiation and augment memory consolidation and retrieval in animal models of AD.Such molecules may be appropriate for use at the first indication of mild cognitive impairment,and perhaps prophylactically in those individuals who are most likely to develop dementia due to genetic,health,behavioral and life-style predisposing factors. 展开更多
关键词 Alzheimer's disease brain-derived neurotrophic factor hepatocyte growth factor Trk receptor Met receptor angiotensin IV dihexa
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