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中医认为痰瘀互结是肝纤维化(hepaticfibrosis,HF)的病机关键,治疗应化痰行瘀法为主。结合临床体会论述了肝纤维化的中医发病机制和治法方药,为中医药治疗肝纤维化从化痰行瘀法来研究提供理论依据。 相似文献
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目的 探讨不同制备方法对痴呆大鼠模型学习记忆能力的影响,为药效评价提供老年期痴呆大鼠模型.方法 40只Wistar雄性大鼠随机分为5组:分期双侧颈总动脉永久结扎后D-半乳糖注射组(A组);D-半乳糖注射后分期双侧颈总动脉永久结扎组(B组);单次双侧颈总动脉永久结扎组(C组);D-半乳糖注射组(D组),正常对照组(E组),每组8只.除E组外,A组左侧颈总动脉结扎,间隔1周后行右侧颈总动脉结扎术;并于结扎术1周后行D-半乳糖腹腔注射(60 mg/kg体重,每天1次),共连续注射42 d;B组腹腔连续注射D-半乳糖(60 mg/kg体重)42 d后,再行双侧颈总动脉永久结扎术;C组仅行双侧颈总动脉永久结扎术42 d,腹腔不注射半乳糖;D组:仅连续腹腔注射D-半乳糖(60 mg/kg体重)42 d,不接扎其双侧颈总动脉.最后采用Morris水迷宫行为学测试法进行定位航行及空间探索实验;取各组大鼠海马CA1区进行电镜观察.结果 与C、E组相比,A、B及D组游泳时间与距离均明显缩短,差异有统计学意义(P<0.01);而A组与B、D组之间差异无统计学意义(P>0.05);比较正常组各模型组海马CA1区锥体细胞有不同程度的丢失,且脑组织病理学改变明显.结论 采用双侧颈总动脉永久结扎联合半乳糖腹腔注射方法,制备的老年期痴呆大鼠模型,记忆力明显减退,且脑组织病理学显著改变,能有效重现老年期痴呆患者的发病特点. 相似文献
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BACKGROUND: Studies on electrical signals of hippocampal brain slices in vivo have shown that matrine inhibits benzylpenicillin sodium-induced activation of neuronal signal transduction.
OBJECTIVE: To verify the inhibition effect of matrine on activation of electrical signals in rat brain slices and the role rnatrine plays in hippocampal amino acid transmitter release.
DESIGN, TIME AND SETTING: The in vitro, neurophysiological, controlled experiment was performed in the Zhejiang Province Key Laboratory of Cardio-cerebrovascular Disease and Nerve System Drugs Appraisement and Chinese Traditional Medicine Screening and Research between July 2003 and May 2004. The in vivo, neuronal, biochemical experiment was performed in the Zhejiang Province Key Laboratory of Chinese Traditional Medicine Quality Standardization from July 2005 to December 2006.
MATERIALS: Forty healthy, Sprague Dawley rats, 7-8 weeks old, and 120 healthy, ICR mice, 5-6 weeks old, were included in this study, irrespective of gender. Matrine powder was provided by the National Institute for the Control of Pharmaceutical and Biological Products, China. Matrine injection was purchased from Zhuhai Biochemical Pharmaceutical Factory, China. Penicillin was bought from Shijiazhuang Pharmaceutical Group Co., Ltd., China.
METHODS: (1) Rats were randomly assigned to four groups: control, penicillin model, and matrine high-dose and low-dose, with 10 rats in each group. The control group was perfused with artificial cerebrospinal fluid. In the remaining three groups, hippocampal brain slices were perfused with normal artificial cerebrospinal fluid containing 1 × 106 U/L penicillin for the first 10 minutes. The penicillin model group received artificial cerebrospinal fluid for an additional 30 minutes, while the matrine high-dose and low-dose groups received 0.1 g/L and 0.05 g/L matrine, respectively, for an additional 30 minutes. (2) Mice were randomly assigned to four groups (n = 30). The matrine high-, medium-, and low-dose groups were separately injected with 58.5, 39.0, and 19.5 mg/kg matrine via caudal vein, respectively. No intervention was administered to the normal group.
MAIN OUTCOME MEASURES: The field potential value in the CA1 region of penicillin-induced rat hippocampal brain slices was analyzed using the evoked field potential technique; chromatography was utilized to determine y-aminobutyric acid and glutamic acid content in the mouse hippocampus.
RESULTS: (1) Both 0.1 g/L and 0.05 g/L matrine reduced the number of evoked field potentials in the penicillin-induced rat hippocampal brain slices (P 〈 0.05 or P 〈 0.01 ). In addition, 0.1 g/L matrine led to a reduction of evoked field potential amplitude (P 〈 0.05). (2) Compared with normal mice, γ-aminobutyric levels were dramatically increased at 20 minutes after high-dose matrine treatment (P 〈 0.05). In addition, significantly increased γ-aminobutyric acid levels were observed at 40 minutes after medium- and low-dose matrine treatments (P 〈 0.05 or P 〈 0.01 ). The glutamic acid/γ-aminobutyric acid ratio was significantly less at 20 minutes after high-dose matrine treatment compared with the normal mice group (P 〈 0.05).
CONCLUSION: Matrine exerts a central inhibitory effect via increased inhibitory neurotransmitter γ-aminobutyric acid levels in the hippocampus. 相似文献
OBJECTIVE: To verify the inhibition effect of matrine on activation of electrical signals in rat brain slices and the role rnatrine plays in hippocampal amino acid transmitter release.
DESIGN, TIME AND SETTING: The in vitro, neurophysiological, controlled experiment was performed in the Zhejiang Province Key Laboratory of Cardio-cerebrovascular Disease and Nerve System Drugs Appraisement and Chinese Traditional Medicine Screening and Research between July 2003 and May 2004. The in vivo, neuronal, biochemical experiment was performed in the Zhejiang Province Key Laboratory of Chinese Traditional Medicine Quality Standardization from July 2005 to December 2006.
MATERIALS: Forty healthy, Sprague Dawley rats, 7-8 weeks old, and 120 healthy, ICR mice, 5-6 weeks old, were included in this study, irrespective of gender. Matrine powder was provided by the National Institute for the Control of Pharmaceutical and Biological Products, China. Matrine injection was purchased from Zhuhai Biochemical Pharmaceutical Factory, China. Penicillin was bought from Shijiazhuang Pharmaceutical Group Co., Ltd., China.
METHODS: (1) Rats were randomly assigned to four groups: control, penicillin model, and matrine high-dose and low-dose, with 10 rats in each group. The control group was perfused with artificial cerebrospinal fluid. In the remaining three groups, hippocampal brain slices were perfused with normal artificial cerebrospinal fluid containing 1 × 106 U/L penicillin for the first 10 minutes. The penicillin model group received artificial cerebrospinal fluid for an additional 30 minutes, while the matrine high-dose and low-dose groups received 0.1 g/L and 0.05 g/L matrine, respectively, for an additional 30 minutes. (2) Mice were randomly assigned to four groups (n = 30). The matrine high-, medium-, and low-dose groups were separately injected with 58.5, 39.0, and 19.5 mg/kg matrine via caudal vein, respectively. No intervention was administered to the normal group.
MAIN OUTCOME MEASURES: The field potential value in the CA1 region of penicillin-induced rat hippocampal brain slices was analyzed using the evoked field potential technique; chromatography was utilized to determine y-aminobutyric acid and glutamic acid content in the mouse hippocampus.
RESULTS: (1) Both 0.1 g/L and 0.05 g/L matrine reduced the number of evoked field potentials in the penicillin-induced rat hippocampal brain slices (P 〈 0.05 or P 〈 0.01 ). In addition, 0.1 g/L matrine led to a reduction of evoked field potential amplitude (P 〈 0.05). (2) Compared with normal mice, γ-aminobutyric levels were dramatically increased at 20 minutes after high-dose matrine treatment (P 〈 0.05). In addition, significantly increased γ-aminobutyric acid levels were observed at 40 minutes after medium- and low-dose matrine treatments (P 〈 0.05 or P 〈 0.01 ). The glutamic acid/γ-aminobutyric acid ratio was significantly less at 20 minutes after high-dose matrine treatment compared with the normal mice group (P 〈 0.05).
CONCLUSION: Matrine exerts a central inhibitory effect via increased inhibitory neurotransmitter γ-aminobutyric acid levels in the hippocampus. 相似文献
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苦参碱(MAtrine)是豆科槐属植物苦参(Sophora flavescnes Ait)、苦豆子(S.Alopecuroides L)、广豆根(S、subprostrata Chunet T、Chen)等中草药的活性成分。作为苦参碱类生物碱的代表,它具有多种药理活性,注射制剂已被广泛用于临床治疗慢性肝炎。近年来国内外在研究苦参碱的过程中,进一步发现了其多方面的药理作用,具有很大的再开发价值。本文在中药苦参醇提取液镇静催眠药理学实验基础上,进行了苦参碱注射液对小鼠脑海马内氨基酸神经递质的作用研究。 相似文献
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