中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Novel Sodium Channel Inhibitor From Leeches

文献类型:期刊论文

作者Lu, Qiumin1,4; Meng, Ping1; Li, Dongsheng1; Luo, Xiaodong3; Sun, Zhaohui5; Rong, Mingqiang1; Wang, Gan1; Long, Chengbo1; Liu, Weihui1; Xu, Cheng1
刊名FRONTIERS IN PHARMACOLOGY
出版日期2018-03-06
卷号9页码:9
ISSN号1663-9812
关键词leech therapy blood-sucking sodium channel pain analgesia
DOI10.3389/fphar.2018.00186
英文摘要Considering blood-sucking habits of leeches from surviving strategy of view, it can be hypothesized that leech saliva has analgesia or anesthesia functions for leeches to stay undetected by the host. However, no specific substance with analgesic function has been reported from leech saliva although clinical applications strongly indicated that leech therapy produces a strong and long lasting pain-reducing effect. Herein, a novel family of small peptides (HSTXs) including 11 members which show low similarity with known peptides was identified from salivary glands of the leech Haemadipsa sylvestris. A typical HSTX is composed of 22-25 amino acid residues including four half-cysteines, forming two intra-molecular disulfide bridges, and an amidated C-terminus. HSTX-I exerts significant analgesic function by specifically inhibiting voltage-gated sodium (Nay) channels (Nav1.8 and Nav1.9) which contribute to action potential electrogenesis in neurons and potential targets to develop analgesics. This study reveals that sodium channel inhibitors are analgesic substances in the leech. HSTXs are excellent candidates or templates for development of analgesics.
资助项目National Natural Science Foundation of China[31630075] ; National Natural Science Foundation of China[31600721] ; National Natural Science Foundation of China[21761142002] ; Chinese Academy of Sciences[SAJC201606] ; Chinese Academy of Sciences[2015CASEABRI002] ; Chinese Academy of Sciences[ZSTH-017] ; Yunnan Province[2016FA006] ; Yunnan Province[2015BC005]
WOS研究方向Pharmacology & Pharmacy
语种英语
出版者FRONTIERS MEDIA SA
WOS记录号WOS:000426696000001
源URL[http://202.127.146.157/handle/2RYDP1HH/4677]  
专题中国科学院武汉植物园
通讯作者Luo, Xiaodong; Sun, Zhaohui; Lai, Ren
作者单位1.Chinese Acad Sci, Kunming Inst Zool, Key Lab Anim Models & Human Dis Mech, Key Lab Bioact Peptides Yunnan Prov, Kunming, Yunnan, Peoples R China
2.Univ Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
3.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming, Yunnan, Peoples R China
4.Chinese Acad Sci, Sino African Joint Res Ctr, Wuhan, Hubei, Peoples R China
5.Guangzhou Gen Hosp Guangzhou Mil Command PLA, Dept Clin Lab, Guangzhou, Guangdong, Peoples R China
6.Nanjing Agr Univ, Life Sci Coll, Nanjing, Jiangsu, Peoples R China
推荐引用方式
GB/T 7714
Lu, Qiumin,Meng, Ping,Li, Dongsheng,et al. Novel Sodium Channel Inhibitor From Leeches[J]. FRONTIERS IN PHARMACOLOGY,2018,9:9.
APA Lu, Qiumin.,Meng, Ping.,Li, Dongsheng.,Luo, Xiaodong.,Sun, Zhaohui.,...&Li, Qiong.(2018).Novel Sodium Channel Inhibitor From Leeches.FRONTIERS IN PHARMACOLOGY,9,9.
MLA Lu, Qiumin,et al."Novel Sodium Channel Inhibitor From Leeches".FRONTIERS IN PHARMACOLOGY 9(2018):9.

入库方式: OAI收割

来源:武汉植物园

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