神经药理学报 ›› 2016, Vol. 6 ›› Issue (2): 37-45.DOI: 10.3969/j.issn.2095-1396.2016.02.007
冯小叶,宋修云,陈乃宏
出版日期:
2016-04-26
发布日期:
2016-05-10
通讯作者:
陈乃宏,男,研究员,博士生导师;研究方向:神经药理学和神经分子生物学;Tel:+86-010-63165177,Fax:+86-010-63165211,E-mail:chennh@imm.ac.cn
作者简介:
冯小叶,女,学士;E-mail:649201711@qq.com
基金资助:
国家自然科学基金项目(No.81274122、No.81373997、No.U1402221),国家“重大新药创制”科技重大专项(No.2012ZX09301002),新药作用机制研究与药效评价北京市重点实验室资助项目(No.BZ0150)
FENG Xiao-ye,SONG Xiu-yun,CHEN Nai-hong
Online:
2016-04-26
Published:
2016-05-10
Contact:
陈乃宏,男,研究员,博士生导师;研究方向:神经药理学和神经分子生物学;Tel:+86-010-63165177,Fax:+86-010-63165211,E-mail:chennh@imm.ac.cn
About author:
冯小叶,女,学士;E-mail:649201711@qq.com
Supported by:
国家自然科学基金项目(No.81274122、No.81373997、No.U1402221),国家“重大新药创制”科技重大专项(No.2012ZX09301002),新药作用机制研究与药效评价北京市重点实验室资助项目(No.BZ0150)
摘要: 缺血性脑卒中具有高发病率、高致死率和高致残率的特点,是严重威胁人类健康的常见疾病之一。中药治疗缺血性脑卒中是中医药学历代积累下来的宝贵财富。牡丹是毛茛科芍药属植物,主要活性部位为牡丹皮和种子,尤其是牡丹皮。中医理论认为,牡丹皮是活血化瘀的良药。现代药理学研究发现,多种牡丹提取单体对缺血性脑卒中具有显著改善作用,提示牡丹活性提取物作为缺血性脑疾病的潜在治疗药物,具有广阔的开发前景和临床应用价值。因此,该文综述近年来牡丹中主要活性单体抗缺血性脑卒中研究进展。
中图分类号:
冯小叶,宋修云,陈乃宏. 牡丹中主要活性单体抗缺血性脑卒中研究进展[J]. 神经药理学报, 2016, 6(2): 37-45.
FENG Xiao-ye,SONG Xiu-yun,CHEN Nai-hong. Research Progress of Peony Main Active Monomers on Cerebral Ischemia[J]. Acta Neuropharmacologica, 2016, 6(2): 37-45.
[1]许舜军, 杨柳, 张勉, 等. 牡丹皮化学成分的液相色谱-飞行时间串联质谱分析[J]. 药学学报, 2006, 41(9): 852-856.[2]He Chun-nian, Yong Peng, Xu Li-jia, et al. Three new oligostilbenes from the seeds of paeonia suffruticosa[J]. Chemical & Pharmaceutical Bulletin, 2010, 41(47): 843-847.[3]刘筱蔼, 吴伟康. 中药防治脑缺血再灌注损伤的研究[J]. 中国中西医结合杂志, 2001, 21(10): 794-796.[4]Cross J L, Meloni B P, Bakker A J, et al. Modes of neuronal calcium entry and homeostasis following cerebral ischemia[J]. Stroke Research & Treatment, 2010, 2010(1): 9.[5]Chen Xing-miao, Chen Han-sen, Xu Ming-jing, et al. Targeting reactive nitrogen species: a promising therapeutic strategy for cerebral ischemia-reperfu-sion injury[J]. Acta Pharmacologica Sinica, 2013, 34(1): 67-77. [6]Ching-Liang Hsieh, Chin-Yi Cheng, Tung-Hu Tsai, et al. Paeonol reduced cerebral infarction involving the superoxide anion and microglia activation in ischemia-reperfusion injured rats[J]. J Ethnopharmacol, 2006, 106(2): 208-215.[7]杨青, 武继彪, 张岫美. 丹皮酚对大鼠脑缺血再灌注损伤炎性细胞因子的作用[J]. 中国生化药物杂志, 2010, 31(2): 111-113.[8]张硕, 高海青, 张岫美. 丹皮酚抑制大鼠局灶性脑缺血再灌注损伤脑组织细胞间黏附分子-1和血管细胞黏附分子-1的表达[J]. 中国生化药物杂志, 2008, 29(1): 5-8.[9]Wu Ji-biao, Song Ning-ning, Wei Xin-bing, et al. Protective effects of paeonol on cultured rat hippocampal neurons against oxygen-glucose deprivation-induced injury[J]. J Neurol Sci, 2008, 264(1-2): 50-55.[10]Zhang G, Yu Z, Zhao H. Protective effect of paeonol on repeated cerebral ischemia in rats[J]. Zhong Yao Cai, 1997, 20(12): 626-628.[11]Su Shan-yu, Cheng Chin-yi, Tsai Tung-Hu, et al. Paeonol protects memory after ischemic stroke via inhibiting β-secretase and apoptosis[J]. Evid Based Complement Alternat Med, 2012, 2012: 932823.[12]杨青, 武继彪, 张岫美. 丹皮酚对大鼠脑缺血再灌注损伤后TLR4及神经细胞凋亡的影响[J]. 中国药学杂志, 2010, 45(17): 1327-1331.[13]韩永涛, 张硕, 张岫美. 丹皮酚减少大鼠局灶性脑缺血再灌注损伤后一氧化氮和内皮素的生成[J]. 中国药学杂志, 2007, 42(16): 1218-1221.[14]Xiao Liang, Wang Ya-zhou, Liu Jing, et al. Effects of paeoniflorin on the cerebral infarction, behavioral and cognitive impairments at the chronic stage of transient middle cerebral artery occlusion in rats[J]. Life Sci, 2005, 78(4): 413-20.[15]刘杰, 华赟鹏, 谭敏谊, 等. 芍药苷注射液对脑缺血-再灌注沙土鼠脑组织中兴奋性氨基酸及腺苷含量的影响[J]. 中药材, 2010, 33(9): 1456-1460.[16]孙蓉, 衣银萍, 吕丽莉, 等. 芍药苷对大鼠全脑缺血模型的影响[J]. 中国中药杂志, 2007, 32(23): 2518-2522.[17]何锦悦, 饶梦琳. 芍药苷对局灶性大鼠脑缺血再灌注脑组织中SOD、Nrf2表达的影响及神经保护作用[J]. 重庆医科大学学报, 2014, 39(2): 178-182.[18]Guo Ruo-bing, Wang Guo-feng, Zhao An-peng, et al. Paeoniflorin protects against ischemia-induced brain damages in rats via inhibiting MAPKs/NF-κB-mediated inflammatory responses[J]. PLoS One, 2012, 7(11): e49701.[19]Jin Lei, Zhang Li-min, Xie Ke-qiang, et al. Paeoniflorin suppresses the expression of intercellular adhesion molecule-1 (ICAM-1) in endotoxin-treated human monocytic cells[J]. Br J Pharmacol, 2011, 164(2b): 694-703.[20]Tang Nou-ying, Chung-Hsiang Liu, Ching-Tou Hsieh, et al. The anti-inflammatory effect of paeoniflorin on cerebral infarction induced by ischemia-reperfusion injury in Sprague-Dawley rats[J]. Am J Chin Med, 2010, 38(1): 51-64.[21]Zhang Guang-qin, Hao Xue-mei, Chen Shi-zhong, et al. Blockade of paeoniflorin on sodium current in mouse hippocampal CA1 neurons[J]. Acta Pharmacol Sin, 2003, 24(12): 1248-1252.[22]王君萍, 韦颖梅. 芍药苷对大鼠脑缺血再灌注损伤细胞凋亡相关基因的影响[J]. 中西医结合心脑血管病杂志, 2008, 6(3): 310-312.[23]Sun Rong, Lv Li-li, Liu Guo-qing. Effects of paeoniflorin on cerebral energy metabolism, nitric oxide and nitric oxide synthase after cerebral ischemia in mongoliagerbils[J]. Zhongguo Zhong Yao Za Zhi, 2006, 31(10): 832-835.[24]Rao Meng-lin, Tang Mi, He Jin-yue, et al. Effects of paeoniflorin on cerebral blood flow and the balance of PGI2/TXA2 of rats with focal cerebral ischemia-reperfusion injury[J]. Yao Xue Xue Bao, 2014, 49(1): 55-60.[25]孙蓉, 吕丽莉. 芍药苷对局灶性脑缺血模型及血脑屏障的影响[J]. 哈尔滨商业大学学报:自然科学版, 2005, 21(4): 405-410.[26]Yuh-Fung Chen, Kuo-Jen Wu, W Gibson Wood. Paeonia lactiflora extract attenuating cerebral ischemia and arterial intimal hyperplasia is mediated by paeoniflorin via modulation of VSMC migration and Ras/MEK/ERK signaling pathway[J]. Evid Based Complement Alternat Med, 2013, 2013(10): 1280-1287.[27]Liu Da-zhi, Xie Ke-qiang, Ji Xin-quan, et al. Neuroprotective effect of paeoniflorin on cerebral ischemic rat by activating adenosine A1 receptor in a manner different from its classical agonists[J]. Br J Pharmacol, 2005, 146(4): 604-611.[28]Hu Zeng-yao, Xu Lan, Yan Rong, et al. Advance in studies on effect of paeoniflorin on nervous system[J]. Zhongguo Zhong Yao Za Zhi, 2013, 38(3): 297-301.[29]Zhong Min, Song Wan-ling, Xu Ye-chun, et al. Paeoniflorin ameliorates ischemic neuronal damage in vitro via adenosine A1 receptor-mediated transactivation of epidermal growth factor receptor[J]. Acta Pharmacol Sin, 2015, 36(3): 298-310.[30]Cai Jiang-hui, Rao Meng-lin, Tang Mi, et al. Protective effect of paeoniflorin on the hippocampus in rats with cerebral ischemia-reperfusion through activating cannabinoid receptor 2[J]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, 2015, 31(4): 443-447.[31]He Xi-hui, Xing Dong-ming, Ding Yi, et al. Effects of cerebral ischemia-reperfusion on pharmacokinetic fate of paeoniflorin after intravenous administration of Paeoniae Radix extract in rats[J]. J Ethnopharmacol, 2004, 94(2-3): 339-344.[32]Cao Chunai, He Xi-hui, Wang Wei, et al. Kinetic distribution of paeoniflorin in cortex of normal and cerebral ischemia-reperfusion rats after intravenous administration of Paeoniae Radix extract[J]. Biomed Chromatogr, 2006, 20(12): 1283-1288.[33]Sun Jing, Li Yun-zi, Ding Yin-hui, et al. Neuroprotective effects of gallic acid against hypoxia/reoxygenation-induced mitochondrial dysfunctions in vitro and cerebral ischemia/reperfusion injury in vivo[J]. Brain Res, 2014, 1589: 126-139.[34]Mehrdad Shahrani Korani, Yaghoub Farbood, Alireza Sarkaki, et al. Protective effects of gallic acid against chronic cerebral hypoperfusion-induced cognitive deficit and brain oxidative damage in rats[J]. Eur J Pharmacol, 2014, 733(3): 62-67.[35]Alireza Sarkaki, H Fathimoghaddam, Seyyed Mohammad Mansouri, et al. Gallic acid improves cognitive, hippocampal long-term potentiation deficits and brain damage induced by chronic cerebral hypoperfusion in rats[J]. Pak J Biol Sci, 2014, 17(8): 978-990.[36]Hyo-Jin Kim, Sang-Chul Ha, Sang-Won Choi. Inhibition of tyrosinase and lipoxygenase activities by resveratrol and its derivatives from seeds of paeonia lactiflora[J]. Journal of Food Science & Nutrition, 2002, 7(4): 447-450.[37]Hyo Jin Kim, Eun Ju Chang, Sung Hee Cho, et al. Antioxidative activity of resveratrol and its derivatives isolated from seeds of Paeonia lactiflora [J]. Biosci Biotechnol Biochem, 2002, 66(9): 1990-1993.[38]Mary S Lopez, Robert J Dempsey, Raghu Vemuganti. Resveratrol neuroprotection in stroke and traumatic CNS injury[J]. Neurochem Int, 2015, 89: 75-82.[39]Veysel Haktan Ozacmak, Hale Sayan-Ozacmak, Figen Barut. Chronic treatment with resveratrol, a natural polyphenol found in grapes, alleviates oxidative stress and apoptotic cell death in ovariectomized female rats subjected to chronic cerebral hypoperfusion[J]. Nutr Neurosci, 2016, 19(4): 176-186.[40]Kevin B Koronowski, Kunjan R Dave, Isabel Saul, et al. Resveratrol preconditioning induces a novel extended window of ischemic tolerance in the mouse brain[J]. Strok, 2015, 46(8): 2293-2298.[41]Meng Zhuang-zhi, Li Jian-guo, Zhao Hong-lin, et al. Resveratrol relieves ischemia-induced oxidative stress in the hippocampus by activating SIRT1[J]. Exp Ther Med, 2015, 10(2): 525-530.[42]Li Wei-na, Tan Chang-hong, Liu Yi, et al. Resveratrol ameliorates oxidative stress and inhibits aquaporin 4 expression following rat cerebral ischemia-reperfusion injury[J]. Mol Med Rep, 2015, 12(5): 7756-7762.[43]Fang Li-qun, Gao Hong-mei, Zhang Wei-na, et al. Resveratrol alleviates nerve injury after cerebral ischemia and reperfusion in mice by inhibiting inflammation and apoptosis[J]. Int J Clin Exp Med, 2015, 8(3): 3219-3226.[44]Anand Kumar Pandey, Pallab Bhattacharya, Sudip Shukla, et al. Resveratrol inhibits matrix metalloproteinases to attenuate neuronal damage in cerebral ischemia: a molecular docking study exploring possible neuroprotection[J]. Neural Regen Res, 2015, 10(4): 568-575.[45]Jeong-Ho Hong, Hyung Lee, Seong-Ryong Lee. Protective effect of resveratrol against neuronal damage following transient global cerebral ischemia in mice[J]. J Nutr Biochem, 2016, 27: 146-152.[46]Dirk M Hermann, Anil Zechariah, Britta Kaltwasser, et al. Sustained neurological recovery induced by resveratrol is associated with angioneurogenesis rather than neuroprotection after focal cerebral ischemia[J]. Neurobiol Dis, 2015, 83: 16-25.[47]Liang Guo-juan, Shi Bin, Luo Wei-nan, et al. The protective effect of caffeic acid on global cerebral ischemia-reperfusion injury in rats[J]. Behav Brain Funct, 2015, 11(1): 1-10.[48]Zhou Yu, Fang San-hua, Ye Yi-lu, et al. Caffeic acid ameliorates early and delayed brain injuries after focal cerebral ischemia in rats[J]. Acta Pharmacologica Sinica, 2006, 27(9): 1103–1110.[49]Woo Seok Yang, Deok Jeong, Young-Su Yi, et al. IRAK1/4-targeted anti-inflammatory action of caffeic acid[J]. Mediators Inflamm, 2013, 2013(1): 153-163. [50]Yu Lu, Chen Chu, Wang Liang-fen, et al. Neuroprotective effect of kaempferol glycosides against brain injury and neuroinflammation by inhibiting the activation of NF-κB and STAT3 in transient focal stroke[J]. Plos One, 2013, 8(2): e55839.[51]Park S E, Sapkota K, Kim S, et al. Kaempferol acts through mitogen-activated protein kinases and protein kinase B/AKT to elicit protection in a model of neuroinflammation in BV2 microglial cells[J]. British J Pharmacology, 2011, 164(3): 1008-1025.[52]Saebyeol Jang, Keith W Kelley, Rodney W Johnson. Luteolin reduces IL-6 production in microglia by inhibiting JNK phosphorylation and activation of AP-1[J]. Proceedings of the National Academy of Sciences USA, 2008, 105(21): 7534-7539.[53]Zhu Li-hong, Bi Wei, Lu Dan, et al. Luteolin inhibits SH-SY5Y cell apoptosis through suppression of the nuclear transcription factor-κB, mitogen-activated protein kinase and protein kinase B pathways in lipopolysaccharide-stimulated cocultured BV2 cells[J]. Experimental & Therapeutic Medicine, 2014, 7(5): 1065-1070.[54]Xu Tong-da, Zhu Hong, Li Dong-ye, et al. Luteolin inhibits angiotensin II-stimulated VSMC proliferation and migration through downregulation of Akt phosphorylation[J]. Evidence-based Complementary and Alternative Medicine, 2015, 2015(1): 9.[55] Carlo Caltagirone, Carlo Cisari, Carlo Schievano, et al. Co-ultramicronized palmitoylethanolamide/luteolin in the treatment of cerebral ischemia: from rodent to man[J]. Translational Stroke Research, 2016, 7(1): 54-69.[56]Irene Paterniti, Daniela Impellizzeri, Rosanna Di Paola, et al. A new co-ultramicronized composite including palmitoylethanolamide and luteolin to prevent neuroinflammation in spinal cord injury[J]. J Neuroinflammation, 2013, 10(1): 12543-12552.[57]Matsuda H, Ohta T, Kawaguchi A, et al. Bioactive constituents of Chinese natural medicines. VI. Moutan cortex. (2): structures and radical scavenging effects of suffruticosides A, B, C, D, and E and galloyl-oxypaeoniflorin[J]. Chem Pharm Bull (Tokyo), 2001, 49(1): 69-72. [58]Lin B. Polyphenols and neuroprotection against ischemia and neurodegeneration[J]. Mini Rev Med Chem, 2011, 11(14): 1222-1238.[59]Liu Ji-kai, Ma Yun-bao, Wu Da-gang, et al. Paeonilide, a novel anti-PAF-active monoterpenoid-derived metabolite from Paeonia delavayi[J]. Biosci Biotechnol Biochem, 2000, 64(7): 1511-1514.[60]吴少华, 马云保, 罗晓东, 等. 丹皮的化学成分研究[J]. 中草药, 2002, 33(8): 9-10.[61]Qian Ling-bo, Fu Jia-yin, Cai Xin, et al. Betulinic acid inhibits superoxide anion-mediated impairment of endothelium-dependent relaxation in rat aortas[J]. J Indian Pharmacology, 2012, 44(5): 588-592.[62]Laura Caltana, Maria Luisa Nieto, Alicia Brusco. Oleanolic acid: a promising neuroprotective agent for cerebral ischemia[J]. Neural Regen Res, 2015, 10(4): 540-541.[63]Kazuo Yamagata, Takuya Kitazawa, Masahiro Shinoda, et al. Stroke status evoked adhesion molecule genetic alterations in astrocytes isolated from stroke-prone spontaneously hypertensive rats and the apigenin inhibition of their expression[J]. Stroke Research & Treatment, 2010, 2010(4).11[64]Myungsuk Kim, Sue Ji Lim, Sarangerel Oidovsambuu, et al. Gnetin H isolated from Paeonia anomala inhibits FcεRI-mediated mast cell signaling and degranulation[J]. J Ethnopharmacol, 2014, 154(3): 798-806. |
[1] | 都保泽, 谭晓虹. 白藜芦醇纳米粒的制备与药理活性研究[J]. 神经药理学报, 2020, 10(3): 8-16. |
[2] | 许家其, 张海红. 广藿香作用的研究进展[J]. 神经药理学报, 2020, 10(3): 27-32. |
[3] | 孙逸, 侯雪芹, 王福刚. 当归芍药散改善认知功能的研究进展[J]. 神经药理学报, 2020, 10(3): 42-46. |
[4] | 张健美, 张丹参. 马勃的化学成分及其药理作用的研究进展[J]. 神经药理学报, 2020, 10(2): 11-14. |
[5] | 钟伟权, 刘佑波, 周才杰, 郑银驹, 邬明利, 梁敏, 张媛媛. 基于网络药理学探讨人参有效成分对骨关节炎的保护作用机制研究[J]. 神经药理学报, 2020, 10(1): 10-16. |
[6] | 宋宜蕾,侯雪芹,郝吉福. 蛇床子现代药理学作用及临床应用的研究进展[J]. 神经药理学报, 2019, 9(6): 58-63. |
[7] | 詹佳虹,简文轩,万江帆,等. 天然化合物治疗缺血性脑卒中抗氧化作用机制的研究进展[J]. 神经药理学报, 2017, 7(6): 60-64. |
[8] | 庞学波,薛茜,邹玉安. 人血浆脂蛋白磷脂酶A2 与缺血性脑卒中的研究进展[J]. 神经药理学报, 2017, 7(4): 31-35. |
[9] | 苏晓梅,张丹参. 人参皂苷-Rg3 的药理作用研究进展[J]. 神经药理学报, 2017, 7(1): 38-44. |
[10] | 李双双,郭春燕. 桃红四物汤化学成分及药理作用研究进展[J]. 神经药理学报, 2016, 6(4): 42-49. |
[11] | 张涛, 张斌, 王佩义, 周涛, 秦雪梅. 定坤丹组方药物化学成分与药理作用研究进展[J]. 神经药理学报, 2015, 5(6): 40-50. |
[12] | 梅艳飞, 张丹参. 丹参酮ⅡA的药理作用及治疗应用研究进展[J]. 神经药理学报, 2014, 4(5): 55-64. |
[13] | 曹欣欣,王书华. 金莲花药理活性及临床应用研究进展[J]. 神经药理学报, 2014, 4(4): 59-64. |
[14] | 郑立卿, 张力, 董晓华,王金. 蛇床子素的药理作用研究进展[J]. 神经药理学报, 2013, 3(6): 33-39. |
[15] | 田慧, 张丹参. 天麻素神经保护机制的研究进展[J]. 神经药理学报, 2013, 3(5): 58-64. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||