Analgesic and anti-inflammatory effects of the amphibian neurotoxin, anntoxin

被引:20
作者
Wei, Lin [1 ]
Dong, Li [2 ,3 ]
Zhao, Tongyan [4 ]
You, Dewen [2 ]
Liu, Rui [1 ]
Hu, Huan [2 ]
Yang, Hailong [2 ]
Lai, Ren [1 ,2 ]
机构
[1] Nanjing Agr Univ, Life Sci Coll, Minist Agr, Key Lab Microbiol Engn Agr Environm, Nanjing 210095, Jiangsu, Peoples R China
[2] Chinese Acad Sci, Kunming Inst Zool, Key Lab Anim Models & Human Dis Mech, Kunming 650223, Yunnan, Peoples R China
[3] Chinese Acad Sci, Grad Sch, Beijing 100009, Peoples R China
[4] Acad Mil Med Sci, Beijing Inst Microbiol & Epidemiol, Beijing, Peoples R China
关键词
Amphibian; Skin; Neurotoxin; Analgesic; Anti-inflammation; GATED SODIUM-CHANNELS; TOAD BOMBINA-MAXIMA; ANTIMICROBIAL PEPTIDES; SKIN SECRETIONS; LEAF EXTRACT; PAIN; PRECURSOR; MODELS; RATS; MICE;
D O I
10.1016/j.biochi.2011.02.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Anntoxin is the first gene-encoded neurotoxin identified from amphibians, which is a 60-residue neurotoxin peptide, acting as an inhibitor of tetrodotoxin-sensitive (TTX-S) voltage-gated sodium channel (VGSC). Sodium channels have been considered as therapeutic targets for pain. Several animal models of persistent inflammatory and neuropathic pain (tail-flick test, hot plate test, acetic acid-induced writhing test, formalin-induced paw licking, carrageenan-induced paw edema) were used to test analgesic functions of recombinant anntoxin (r-anntoxin). In all these animal models, r-anntoxin showed strong analgesic functions. R-anntoxin obviously inhibited secretions of both tumor necrosis factor alpha (TNF-alpha) and cyclooxygenase-2 (COX-2). Histopathological study indicated that r-anntoxin reduced the edematous epidermis induced by carrageenan. All these results indicate that r-anntoxin has strong analgesic and anti-inflammatory activities. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:995 / 1000
页数:6
相关论文
共 35 条
[1]  
BEUTLER B, 1989, ANNU REV IMMUNOL, V7, P625, DOI 10.1146/annurev.iy.07.040189.003205
[2]   Animal peptides targeting voltage-activated sodium channels [J].
Billen, Bert ;
Bosmans, Frank ;
Tytgat, Jan .
CURRENT PHARMACEUTICAL DESIGN, 2008, 14 (24) :2492-2502
[3]   International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels [J].
Catterall, WA ;
Goldin, AL ;
Waxman, SG .
PHARMACOLOGICAL REVIEWS, 2005, 57 (04) :397-409
[5]   Multiple bradykinin-related peptides from the skin of the frog, Rana temporaria [J].
Conlon, JM ;
Aronsson, U .
PEPTIDES, 1997, 18 (03) :361-365
[6]   Antimicrobial peptides from ranid frogs: taxonomic and phylogenetic markers and a potential source of new therapeutic agents [J].
Conlon, JM ;
Kolodziejek, J ;
Nowotny, N .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2004, 1696 (01) :1-14
[7]   Sodium Channels in Normal and Pathological Pain [J].
Dib-Hajj, Sulayman D. ;
Cummins, Theodore R. ;
Black, Joel A. ;
Waxman, Stephen G. .
ANNUAL REVIEW OF NEUROSCIENCE, VOL 33, 2010, 33 :325-347
[8]   Voltage-Gated Sodium Channels: Therapeutic Targets for Pain [J].
Dib-Hajj, Sulayman D. ;
Black, Joel A. ;
Waxman, Stephen G. .
PAIN MEDICINE, 2009, 10 (07) :1260-1269
[9]   STUDIES OF MEDIATORS OF ACUTE INFLAMMATORY RESPONSE INDUCED IN RATS IN DIFFERENT SITES BY CARRAGEENAN AND TURPENTINE [J].
DIROSA, M ;
GIROUD, JP ;
WILLOUGHBY, DA .
JOURNAL OF PATHOLOGY, 1971, 104 (01) :15-+
[10]   Roles of diversifying selection and coordinated evolution in the evolution of amphibian antimicrobial peptides [J].
Duda, TF ;
Vanhoye, D ;
Nicolas, P .
MOLECULAR BIOLOGY AND EVOLUTION, 2002, 19 (06) :858-864