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| 1 | Anti-amnestic and anti-aging effects of ginsenoside Rg1 and Rb1 and its mechanism of action显示文摘In the present paper, we overview the discovery of new biological activities induced by ginsenoside Rg 1 and Rb 1 and discuss possible mechanisms of action. Both compounds could increase neural plasticity in efficacy and structure; especially Rg 1, as one small molecular drug, can increase proliferation and differentiation of neural progenitor cells in dentate gyrus of hippocampus of normal adult mice and global ischemia model in gerbils. This finding has great value for treatment of Alzheimer's disease and other neurodegenerative disorders which is characterized by neurons loss. Increase of expression of brain derived neurotrophic factor, Bcl-2 and antioxidant enzyme, enhanced new synapse formation, inhibition of apoptosis and calcium overload are also important neuron protective factors. Rgl and Rbl have common effects, but there are some differences in pharmacology and mechanism. These differences may attribute to their different chemical structure. Rg 1 is panaxtriol with two sugars, while Rb 1 is panaxtriol with four | YongCHENG Li-hongSHEN Jun-tianZHANG | 2005 | Acta Pharmacologica Sinica2005，26，2： | 86 |
| 2 | Therapeutic effects of berberine in impaired glucose tolerance rats and its influence on insulin secretion显示文摘AIM: To explore the anti-diabetic effects of berberine and its influence on insulin secretion. METHODS: Impaired glucose tolerance rats induced by iv injection of streptozotocin 30 mg/kgwere treated with berberine 187.5 and 562.5 mg/kg while fed with high fat laboratory chow. After rats were treated for 4 weeks, oral glucose tolerance was determined, and for 8 weeks, the fasting blood glucose, insulin, lipid series were determined. In insulin secretion experiments, berberine 93.75, 187.5, and 562.5 mg/kg was administered orally to BALB/c mice at a bolus. The murine serum was collected 2 h after the berberine administration for insulin determination. Insulin released from HIT-T15 cells and pancreatic islets incubated with berberine 1-100 μmol/L for 12 h was determined. RESULTS: The levels of fasting blood glucose (7.4±1.5 or 7.3±1.3 vs 9.3±1.3 mmol/L), triglycerides (0.61±0.22 or 0.63± 0.17 vs 1.8±0.7 mmol/L), total cholesterol (1.8±0.3 or 1.9±0.3 vs 2.2±0.2 mmol/L), free fatty acid (456±93 or 460±72 vs 550±113 μmol/L) and apolipoprotein B (0.37±0.02 or 0.42±0.05 vs 0.46±0.04 g/L) were reduced greatly in berberine-treated groups at doses of 187.5 and 562.5 mg·kg-1·d-1, respectively as compared with those in control group (P<0.05 or P<0.01),whereas high densitylipoprotein-cholesterol (1.5±0.3 or 1.4±0.3vs 1.1±0.1 g/L), apolipoprotein AI (0.80±0.08 or 0.87±0.08 vs 0.71±0.06 g/L) were significantly increased (P<0.05 or P<0.01), and oral glucose tolerance was improved. In vitro experiment showed that berberine 1-10 μmol/L facilitated insulin secretion of HIT-T15 cells and murine pancreatic islets in a dose-dependent manner. Meanwhile murine serum insulin level (27.5±2.7 or 29±4 or 29±4 vs 24.3±2.8 pIU/L) was undoubtedly promoted and blood glucose (4.52±0.31 or 4.45±0.29 or 4.30±0.19 vs 4.87±0.21 mmol/L) was reduced after berberine administration at doses of 93.75, 187.5, and 562.5 mg/kg, respectively in the BALB/c mice. CONCLUSION: Berberine possesses anti-diabetic effects, which is related to the property of stimulating insulin secretion and modulating lipids. | San-huaLENG Fu-erLU Li-junXU | 2004 | Acta Pharmacologica Sinica2004，25，4： | 133 |
| 3 | Anti-tumor and immunoregulatory activities of Ganoderma lucidum and its possible mechanisms显示文摘Ganoderma lucidum (G lucidum) is a medicinal fungus with a variety of biological activities. It has long been used as a folk remedy for promotion of health and longevity in China and other oriental countries. The most attractive character of this kind of medicinal fungus is its immunomodulatory and anti-tumor activities. Large numbers of studies have shown that G lucidum modulate many components of the immune system such as the antigen-presenting cells, NK cells, T and B lymphocytes. The water extract and the polysaccharides fraction of G lucidum exhibited significant anti-tumor effect in several tumor-bearing animals mainly through its immunoenhancing activity. Recent studies also showed that the alcohol extract or the triterpene fraction of G lucidum possessed antitumor effect, which seemed to be related to the cytotoxic activity against tumor cells directly. Preliminary study indicated that antiangiogenic effect may be involved antitumor activity of G lucidum. | Zhi-binLIN Hui-naZHANG | 2004 | Acta Pharmacologica Sinica2004，25，11： | 72 |
| 4 | Hypoxla inducible factor 1 (HIF-1) and cardioprotection显示文摘 | Demet TEKIN Ali D DURSUN Lei XI | 2010 | Acta Pharmacologica Sinica2010，31，9： | 62 |
| 5 | Endoplasmic reticulum stress: a novel mechanism and therapeutic target for cardiovascular diseases显示文摘Endoplasmic 蜂窝胃是负责合拢, translational 以后修正和运输的一个主要细胞器能分泌,钠和膜蛋白质,这样 palys 在维持细胞的动态平衡的重要罗音。Endoplasmic 蜂窝胃应力(ERS ) 是被 unfolded/misfolded 蛋白质的累积在 endoplasmic 蜂窝胃环境骚乱以后加速的一个条件,由许多生理、病理学的因素被触发例如滋养的剥夺,改变了 glycosylation,钙弄空,氧化压力, DNA 损坏和精力骚乱,等等。ERS 们可以开始展开的蛋白质反应(UPR ) 恢复细胞的动态平衡或导致 apoptosis。众多的研究澄清了在 ERS 和心血管的疾病之间的连接。这评论集中于参予的嗯联系分子的机制生理并且心和血容器的 pathophysiological 过程。另外,调整 ERS 的很多药被介绍,它可以被用来治疗心血管的疾病。这评论可以为学习心血管的疾病的致病并且发现指向 ERS 的新奇的药打开新大街。 | Mei-qing LIU Zhe CHEN Lin-xi CHEN | 2016 | Acta Pharmacologica Sinica2016，37，4： | 65 |
| 6 | New knowledge of the mechanisms of sorafenib resistance in liver cancer显示文摘Sorafenib 是压制肿瘤房间增长和 angiogenesis 并且支持肿瘤房间 apoptosis 的一个口头的 multikinase 禁止者。它被 FDA 在 2006 为先进肾的房间癌的治疗同意,并且作为为在 2007 的先进 hepatocellular 癌(HCC ) 的唯一的目标药。Sorafenib 能显著地扩大病人,但是仅仅由 3-5 月的中部的幸存时间。而且,它与抵抗经常开发的严肃的不利副作用,和药被联系。因此,探索位于 sorafenib 抵抗下面的机制并且为应付这些问题开发个性化的治疗学的策略是很重要的。最近的研究表明了除了主要抵抗,几机制正在位于获得的抵抗下面到 sorafenib,例如包含 PI3K/Akt 和 JAK-STAT 小径,组织缺氧可诱导的小径的激活,和上皮间充质的转变的串音。这里,我们简短为药抵抗描述 sorafenib,它的临床的应用程序,和分子的机制的函数,特别为 HCC 病人。 | Yan-jing ZHU Bo ZHENG Hong-yang WANG Lei CHEN | 2017 | Acta Pharmacologica Sinica2017，38，5： | 65 |
| 7 | Salvia miltiorrhiza Burge (Danshen): a golden herbal medicine in cardiovascular therapeutics显示文摘鼠尾草植物 miltiorrhiza Burge (Danshen ) 是拥有宽广心血管、脑血管的保护的行动的著名药用的植物并且为许多世纪在亚洲国家被使用了。积累的证据建议特别地, Danshen 和它的部件阻止脉管的疾病动脉粥样硬化和心脏病,包括的心肌的梗塞,心肌的 ischemia/reperfusion 损害,心律不齐,心脏的肥大和心脏的纤维变性。出版文学显示那脂性的成分( tanshinone 我, tanshinone IIa , tanshinone IIb , cryptotanshinone , dihydrotanshinone ,等等)象吸水的成分一样( danshensu , salvianolic 酸 A 和 B , protocatechuic 醛,等等)贡献 Danshen 的心血管的保护的行动,在这些成分之中建议潜在的协同。此处,我们在心血管的行动和 Danshen 的主要 pharmacologically 活跃的成分的治疗学的潜力以后提供系统的新评论。这些 bioactive 混合物将在小分子的心血管的药发现用作优秀的药候选人。这篇文章也为在心血管的治疗学理解 Danshen 的传统的使用提供一个科学基本原理。 | Zhuo-ming LI Suo-wen XU Pei-qing LIU | 2018 | Acta Pharmacologica Sinica2018，39，5： | 75 |
| 8 | Heart-type fatty acid binding protein (H-FABP) as a biomarker for acute myocardial injury and long-term post-ischemic prognosis显示文摘尖锐心肌的梗塞(AMI ) 是一个威胁生活的事件。甚至与及时处理,尖锐 ischemic 心肌的损害和随后的局部缺血灌注损害(IRI ) 能仍然是困难的问题处理。除了放射学并且另外的辅助考试,适用的心脏的 biomarkers 的实验室测试为这混乱监视的早诊断和结束也是必要的。心类型丰满的酸绑定蛋白质(H-FABP ) 主要在 cardiomyocytes 内存在,最近为心肌的损害作为潜在地有希望的 biomarker 出现了。在这评论,我们在对心肌的损害和 IRI 的评价讨论 H-FABP 的敏感和特性,特别在早阶段,和它与另外的通常使用的心脏的 biomarkers 比较的长期的预示的价值,包括肌球素( Mb ),心脏的 troponin 我( cTnI ),肌酸 kinase MB ( CK-MB ),C反应的蛋白质( CRP ),肝糖 phosphorylase isoenzyme BB ( GPBB ),和高敏感的心脏的 troponin T ( hs-cTnT )。有另外的 biomarkers 的 H-FABP 的联合申请的潜力和值也被讨论。最后, H-FABP 的前景被总结;几个技术问题被讨论在临床的实践便于 H-FABP 的更宽的申请。 | Xiao-dong YE Yi HE Sheng WANG Gordon T WONG Michael G IRWIN Zhengyuan XIA | 2018 | Acta Pharmacologica Sinica2018，39，7： | 72 |
| 9 | Morinda citrifolia (Noni): A literature review and recent advances in Noni research^1显示文摘Morinda citrifolia L(Noni) has been used in folk remedies by Polynesians for over 2000 years,and is reported to have a broad range of therapeutic effects,including antibacterial,antiviral,antifungal,antitumor,antihelmin,analgesic,hypotensive,anti-inflammatory,and immune enhancing effects.In order to reveal the nutritional and medicinal value of the Noni plant,and to summarize scientific evidence that supports the Polynesians' claim,a literature review and recent advances in Noni research is given below. | Brett J WEST CJarakae JENSEN Diane NOWICKI SU Chen Afa K PALU Gary ANDERSON | 2002 | Acta Pharmacologica Sinica2002，23，12： | 80 |
| 10 | Learning of medical pharmacology via innovation:a personal experience at McMaster and in Asia显示文摘Pharmacology in the traditional medical curriculum has been treated as a discrete “preclinical” discipline identifying itself distinctly different from the other preclinical sciences or clinical subjects in knowledge base as well as learning/teaching instructions. It is usually run in series with other pre-clinical courses (eg, anatomy, biochemistry, physiology etc), but in parallel with other paraclinical courses such as pathology, microbiology and community medicine. Clinical pharmacology was only introduced relatively recently designed to overcome the perceived deficiency in “preclinical” pharmacology regarding its therapeutic relevance and application to medicine. In many universities, both preclinical and clinical pharmacology courses co-exist, usually independently offered by two separate, sometimes non-interacting Departments of Pharmacology and Clinical Pharmacology. In this model, pharmacology is generally taught in a teacher-centered, discipline-oriented, and knowledge-based curriculum. Furthermore, pharmacology courses are commonly taught by “expert” teachers, who usually engage in excessive-teaching, often adopt a knowledge-based approach in both instruction and assessment, and frequently evade or ignore clinical relevance. The clinical relevance of the pharmacological sciences is sometimes also taught in a didactic and problem-solving manner, although it is usually case-oriented. In recent years, problem-based medical curricula have emerged, in varying forms, as a platform in which pharmacology is viewed as an integrated component in a holistic approach to medical education. In this problem-based learning (PBL) model, pharmacology is learned in a student-centered environment, based on self-directed, clinically relevant and case-oriented approach, usually in a small-group tutorial format. In PBL, pharmacology is learned in concert with other subject issues relevant to the case-problem in question, such as anatomy, physiology, pathology, microbiology, population health, behavior science, etc. Students learn via problem-evoked curiosity and motivation, in an environment which encourages free inquiries and intensive discussions in a cooperative rather than competitive atmosphere. Teachers facilitate students' learning objectives rather than deliver pre-packed knowledge and dictate what they think students should learn. Based on the above two models, a change towards PBL curriculum appears to be beneficial in better preparing the medical students as life-long learners capable of coping with changes in knowledge and skills associated with the progressive and dynamic social/economic transformation in the Asia-Pacific regions. Evidence is presented that this is indeed happening. | Chiu-yin KWAN | 2004 | Acta Pharmacologica Sinica2004，25，9： | 56 |
| 11 | Hypoglycemic effect of Astragalus polysaccharide and its effect on PTP1B显示文摘Aim: To examine the effects ofAstragalus polysaccharide (APS), a component of an aqueous extract ofAstragalus membranaceus roots, on protein tyrosine phosphatase 1B (PTP1B), a negative regulator of insulin-receptor (IR) signal transduction, and its potential role in the amelioration of insulin resistance. Methods: Ten-week-old fat-fed streptozotocin (STZ)-treated rats, an animal model of type Ⅱ diabetes mellitus (TIIDM), were treated with APS (400 mg/kg po) for 5 weeks. Insulin sensitivity was identified by the insulin-tolerance test. Further analyses on the possible changes in insulin signaling occurring in skeletal muscle and liver were performed by immunoprecipitation or Western blotting. PTP1B activity was measured by an assay kit. Results: The diabetic rats responded to APS with a significant decrease in body weight, plasma glucose, and improved insulin sensitivity. The activity and expression of PTP1B were elevated in the skeletal muscle and liver of TIIDM rats. Thus the insulin signaling in target tissues was diminished. APS reduced both PTP1B protein level and activity in the muscle, but not in the liver of TIIDM rats. Insulin-induced tyrosine phosphorylation of the IR β-subunit and insulin receptor substrate-1 (IRS-1) were increased in the muscle, but not in the liver of APS-treated TIIDM rats. There was no change in the activity or expression of PTP1B in APS-treated normal rats, and blood insulin levels did not change in TIIDM rats after treatment with APS. Conclusion: APS enables insulin-sensitizing and hypoglycemic activity at least in part by decreasing the elevated expression and activity of PTP1B in the skeletal muscles of TIIDM rats. | YongWU Jing-pingOU-YANG KeWU YaWANG Yun-fengZHOU Chong-yuanWEN | 2005 | Acta Pharmacologica Sinica2005，26，3： | 58 |
| 12 | Advances in the study of berberine and its derivatives: a focus on anti-inflammatory and anti- tumor effects in the digestive system显示文摘它广泛地被认出了那发炎,特别地长期的发炎,能增加癌症的风险并且发炎和癌症的同时的治疗可以生产优秀治疗学的效果。Berberine,从根茎 coptidis 孤立的碱,有宽广应用程序,特别地作为在有长历史的诊所的一个抗菌剂代理人。在过去的十年,许多报告证明了这个自然产品和它的衍生物对癌症和发炎举办高活动。在这评论,我们在在消化系统装饰 berberine 和它同样反煽动性的衍生物和反肿瘤代理人总结进展;我们也讨论他们的结构活动关系。这些数据应该作为有反发炎活动的新奇 anticancer 药为这个自然产品的发展是有用的。 | Kun ZOU Zhao LI Yong ZHANG Hao-yue ZHANG Bo LI Wei-liang ZHU Ji-ye SHI Qi JIA Yi-ming LI | 2017 | Acta Pharmacologica Sinica2017，38，2： | 58 |
| 13 | 杜仲和西伯利亚人参的化学成分及药理作用(英文)显示文摘The bark and leaves of Eucommia ulmoides Oliv(Eucommiaceae) and 'Siberian ginseng' (Ezoukogi inJapanese) prepared from the root bark or stem bark ofEleutherococcus senticosus Maxim (Acanthopanax senti-cosus Harms) have been used as tonic and anti-stressdrug. The extracts of Eucommia showed anti-hyperten-sive, anti-complementary, anti-oxidative, and anti-gastric ulcer effects, and promting collagen synthesis,accelating granuloma formation, and other pharmacologi-cal effects. The Siberian ginseng exhibited anti-fatigue,anti-stress, immuno-enhancing effect, CNS activity, andanti-depressive effect. By now, 40, 28, and 10 com-pounds have been isolated from Eucommia ulmoidesbark, Eucommia ulmoides leavs, and Siberian ginseng,respectively, and their structures were elucidated. Theirpharmacological activities were mainly due to lignans andiridoid glycosides. | DEYAMA Takeshi NISHIBE Sansei NAKAZAWA Yoshihisa | 2001 | Acta Pharmacologica Sinica2001，22，12： | 52 |
| 14 | Effect of curcumin on multidrug resistance in resistant human gastric carcinoma cell line SGC7901/VCR显示文摘瞄准:调查杂种狗枯茗的颠倒效果在上多,在一个抵抗的人的胃的癌房间的药抵抗(MDR ) 排队。方法:长春新碱(VCR ) 的细胞毒素的效果被 MTT 试金评估。VCR 导致的房间 apoptosis 被染色的 propidium 碘化物(PI ) 决定流动血细胞计数(FCM ) 和用吖啶橙(AO ) 的词法试金 /ethidium 溴化物(EB ) 双染色。P-glycoprotein (P-gp ) 功能被 rhodamine123 (Rh123 ) 的累积和流出用 FCM 表明。P-gp 的表示和 caspase-3 的激活被 FCM 用结合的荧光黄异硫氰酸盐(FITC ) 测量 anti-P-gp 和劈开反的 caspase-3 抗体分别地。结果:在 5 micromol/L, 10 micromol/L,或 20 micromol/L 的集中,姜黄色素没在胃的癌房间线(SGC7901 ) 或它的 VCR 抵抗的变体房间衬里的一个父母人(SGC7901/VCR ) 上有细胞毒素的效果。SGC7901/VCR 房间的 VCR-IC50 价值是多于 SGC7901cells 的 45 次, SGC7901/VCR 房间显示出 apoptotic 抵抗到 VCR。与 5 micromol/L, 10 micromol/L,或 20 micromol/L 杂种狗枯茗对待的 SGC7901/VCR 房间减少了以一种剂量依赖者方式的 VCR 和支持的调停 VCR 的 apoptosis 的 IC50 价值。姜黄色素(10 micromol/L ) 增加了 Rh123 累积并且在 SGC7901/VCR 房间禁止了 Rh123 的流出,但是没在 SGC7901 房间改变 Rh123 的累积和流出。P-gp 完了在 SGC7901/VCR 表示了房间,而它低与杂种狗枯茗(10 micromol/L ) 在一个 24-h 处理以后调整了。独自与 1 mumol/L VCR 对待的抵抗房间在 44% 增加的抵抗房间线相对 caspase-3 的 SGC7901 房间,而是激活看了 caspase-3 激活的 77% 底层房间什么时候与杂种狗枯茗在联合与 VCR 被对待。结论:姜黄色素能颠倒人的胃的癌 SGC7901/VCR 房间线的 MDR。这可能与减少的 P-gp 被联系函数和表达式,和在 MDR 房间的 caspase-3 激活的提升。 | Xiao-qing TANG Hu BI Jian-qiang FENG Jian-guo CAO | 2005 | Acta Pharmacologica Sinica2005，26，8： | 49 |
| 15 | Molecular mechanism and regulation of autophagy显示文摘Autophagy 在真核细胞的房间是为长寿蛋白质和细胞质的细胞器的降级的一条主要细胞的小径。包括氨基酸饥饿和微生物的侵略,很多细胞内部 / 细胞外的刺激能在房间导致 autophagic 反应。在酵母的基因极大地预付我们参予 autophagy 和基因的分子的机制的理解的 ATG 的发现在调整 autophagic 小径包含了。许多酵母基因有哺乳动物的相当或相同的事物,建议为 autophagy 的基本机械 evolutionarily 沿着真核细胞的门被保存了。autophagy 的规定是一个很复杂的过程。许多发信号的小径包括 rapamycin (岩山) 的目标或 rapamycin (mTOR ) 的哺乳动物的目标, phosphatidylinositol 3-kinase-I (PI3K -- 我)/PKB, GTPases,钙和蛋白质合成都在调整 autophagy 起重要作用。autophagy 的分子的机制和规定在这评论被讨论。 | 2Ya-ping YANG Zhong-qin LIANG Zhen-lun GU Zheng-hong QIN | 2005 | Acta Pharmacologica Sinica2005，26，12： | 50 |
| 16 | Effect of TGF-β/Smad signaling pathway on lung myofibroblast differentiation显示文摘目的: Myofibroblasts 玩在 lungfibrosis.Transforming 生长的致病的重要角色因素( TGF ) -beta1 广泛地作为表明 TGF-beta1 的小径的一个关键 fibrogeniccytokine.The 学生被认出了通过细胞质的 Smad proteins.Our studyinvestigated 单个TGF-的角色(在调停的 beta1/Smad 信号蛋白质alpha光滑的 muscleactin ( alpha-SMA )基因表示,它是 myofibroblastdifferentiation.Methods 的一个著名关键标记:我们短暂地,在 TGF-beta1-treated 人的 fetallung fibroblasts.We 的 cotransfected a-SMA 倡导者酶熔化 plasmid (p895-Luc ) 和 Smad 表达式 plasmids 和测量 Luc 活动由 bleomycin.alpha-SMA proteinexpression 导致了 Smad3 猛烈鼠标肺纤维变性被西方的 blotting.Collagen 估计蛋白质被 measuringhydroxyprolin.Myofibroblast 形态学分析被 immunohistochemistry.Results 估计:我们发现 thatthe Smad3 的 overexpression ,不是而主导的 negativemutant Smad3 和 Smad7 的在表示上镇压了, Smad2 显著地在 vitro 增加了 TGF-beta1-induced alpha-SMA promoteractivity 和 a-SMA 蛋白质表示 TGF-beta1 导致了 alpha-SMA 基因 expression.Compared 到 wild-typemice , Smad3 猛烈老鼠在 bleomycin 处理以后显示出稀释的肺纤维变性,表明的 bylower 骨胶原生产和 myofibroblast differentiation.Conclusion :我们的学习 suggestedTGF-beta1/Smad3 是调整了为未来的潜在的意义 attenuating 尝试的 myofibroblast differentiation.This resultindicates 的一条主要小径由 Smad3 串联的抑制的人的 lungfibrosis 的前进。 | Li GU Yuan-jue ZHU Xiao YANG Zi-Jian GUO Wen-bing XU Xin-lun TIAN | 2007 | Acta Pharmacologica Sinica2007，28，3： | 47 |
| 17 | Cardioprotection of sevoflurane postconditioning by activating extracellular signal-regulated kinase 1/2 in isolated rat hearts^1显示文摘瞄准:1/2 免于的细胞外的调整信号的 kinase (英皇家空军之阶级最低之兵) 的激活是化学家灌注损害。ERK1/2 是否调停 sevoflurane 柱子调节的 cardioprotection 是未知的。我们测试了 sevoflurane 柱子调节是否经由 ERK1/2-depen-dent 机制生产 cardioprotection。方法:在协议 1 , 酒Langendorff 的 Sprague Dawley 老鼠心( n=84 , 12 每组)与假冒的组的异常,受到 90 min 灌注跟随的 30 min 局部缺血并且被分到未经治疗(控制)组,由 4 个周期列在后面是化学家帖子调节(各个的 25 s ),3%( v/v ) sevoflurane 帖子调节(为 5 min 和冲刷的 10 min ),并且 PD98059 溶剂 DMSO (<0.2%), ERK1/2 禁止者 PD98059 ( 20 μmol/L ),和 Sevo+PD 管理。在平衡的 30 min 的左室的 hemodynamics 和冠的流动分别地在灌注的 30, 60,和 90 min 被记录。尖锐梗塞尺寸被 triphenyltetrazolium 氯化物染色测量。线粒体的配置被一台电子显微镜观察。西方的污点分析被用来在灌注的结束决定 cytosolic 和 mitochondrial 细胞色素 c 的内容。在协议 2,在灌注的 15 min 以后,总数的表示和 ERK1/2 和它的下游的目标 p70S6K 的 phosphorylated 形式由西方的弄污是坚定的。结果:在基线 hemodynamics 的差别都没在试验性的组(P>0.05 ) 之中被观察。在灌注以后,与控制组相比, sevoflurane 柱子调节并且显著地是化学家柱子调节(P<0.05 ) 改进了功能的恢复并且(P<0.05 ) 大部分减少了心肌的梗塞尺寸(22.9%± 4 .6% 和 21.2%± 3 .8% ,对 39.4%± 5 .7% ,两 P<0.05 ) 。调停 Sevoflurane 的保护被 PD98059 废除。结论:由 sevoflurane 的麻药柱子调节有效地由在 vitro 激活 ERK1/2 免于灌注损坏。 | Hong-tao CHEN Cheng-xiang YANG Heng LI Cheng-jing ZHANG Xian-jie WEN Jun ZHOU You-ling Fan Teng HUANG Yin-ming ZENG | 2008 | Acta Pharmacologica Sinica2008，29，8： | 41 |
| 18 | RNA interference-mediated downregulation of Beclinl attenuates cerebral ischemic injury in rats显示文摘 | Yong-qiu ZHENG Jian-xun LIU Xin-zhi LI Li XU Yong-gang XU | 2009 | Acta Pharmacologica Sinica2009，30，7： | 42 |
| 19 | Pharmacological actions and therapeutic applications of Salvia miltiorrhiza depside salt and its active components显示文摘鼠尾草植物 miltiorrhiza,作为 danshen 知道的传统的医药植物,广泛地在中国被使用了到改进血循环,减轻血壅滞,并且治疗冠的心疾病。S miltiorrhiza depside 盐是最近在 Materia Medica 的上海研究所开发的新奇的药;它包含镁 lithospermate B (MLB ) 和它的类似物, rosmarinic 酸(RA ) 和 lithospermic 酸(LA ) ,活跃部件。这药在诊所被使用了改进血循环并且治疗冠的心疾病。从 S miltiorrhiza 和它的部件的 depside 盐的药理学效果广泛地被调查了。试验性的研究证明了镁 lithospermate B 拥有许多生物活动,在象对心肌的 ischemia-reperfusion 损害的动脉粥样硬化和保护的变细那样的心血管的系统的特别保护的效果。Rosmarinic 酸和 lithospermic 酸也在心血管的系统上显示出有益的效果。这份报纸关于位于 S miltiorrhiza depside 盐的活跃部件的药理学行动下面的机制考察最近的调查结果,基于出版工作和我们的自己的观察。 | Wen-yu WU Yi-ping WANG | 2012 | Acta Pharmacologica Sinica2012，33，9： | 47 |
| 20 | Inflammatory responses in hypoxic ischemic encephalopathy显示文摘 | Fudong Liu Louise D McCullough | 2013 | Acta Pharmacologica Sinica2013，34，9： | 45 |
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