Drugs From the Sea: Conotoxins as Drug Leads for Neuropathic Pain and Other Neurological Conditions

被引:56
作者
Alonso, D. [1 ]
Khalil, Z. [2 ]
Satkunanathan, N. [2 ]
Livett, B. G. [3 ]
机构
[1] NeuroPharma SA, Avda Ind 52, Madrid 28760, Spain
[2] Univ Melbourne, Natl Aging Res Inst, Melbourne, Vic 3010, Australia
[3] Univ Melbourne, Dept Biochem & Mol Biol, Melbourne, Vic 3010, Australia
关键词
D O I
10.2174/1389557033487746
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The oceans are a source of a large group of structurally unique natural products that are mainly found in invertebrates such as sponges, tunicates, bryozoans, and molluscs. It is interesting to note that the majority of marine compounds currently in clinical trials or under preclinical evaluation are produced by these species rather than as secondary metabolites from algae [1]. Through the combined efforts of marine natural products chemists and pharmacologists a number of promising compounds have been identified that are either already at advanced stages of clinical trials such as the new anti-cancer drug marine alkaloid ecteinascidin 743 [2], or have been selected as promising candidates for extended preclinical evaluation [3]. This is the case for conotoxins, (Table 1) where a number of conopeptides are currently being developed as analgesics for the treatment of neuropathic pain.
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收藏
页码:785 / 787
页数:3
相关论文
共 36 条
[1]   ω-conotoxin CVID inhibits a pharmacologically distinct voltage sensitive calcium channel associated with transmitter release from preganglionic nerve terminals [J].
Adams, DJ ;
Smith, AB ;
Schroeder, CI ;
Yasuda, T ;
Lewis, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (06) :4057-4062
[2]  
Adams DJ, 1999, DRUG DEVELOP RES, V46, P219
[3]   α-Conotoxins [J].
Arias, HR ;
Blanton, MP .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (10) :1017-1028
[4]   Ziconotide, a new N-type calcium channel blocker, administered intrathecally for acute postoperative pain [J].
Atanassoff, PG ;
Hartmannsgruber, MWB ;
Thrasher, J ;
Wermeling, D ;
Longton, W ;
Gaeta, R ;
Singh, T ;
Mayo, M ;
McGuire, D ;
Luther, RR .
REGIONAL ANESTHESIA AND PAIN MEDICINE, 2000, 25 (03) :274-278
[5]  
BINGHAM JP, 1996, BIOCH ASPECTS MARINE, P13
[6]   Pharmacotherapeutic potential of omega-conotoxin MVIIA (SNX-111), an N-type neuronal calcium channel blocker found in the venom of Conus magus [J].
Bowersox, SS ;
Luther, R .
TOXICON, 1998, 36 (11) :1651-1658
[7]   δ-conotoxin structure/function through a cladistic analysis [J].
Bulaj, G ;
DeLaCruz, R ;
Azimi-Zonooz, A ;
West, P ;
Watkins, M ;
Yoshikami, D ;
Olivera, BM .
BIOCHEMISTRY, 2001, 40 (44) :13201-13208
[8]   Origins of diverse feeding ecologies within Conus, a genus of venomous marine gastropods [J].
Duda, TF ;
Kohn, AJ ;
Palumbi, SR .
BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, 2001, 73 (04) :391-409
[9]   α-conotoxins:: Nicotinic acetylcholine receptor antagonists as pharmacological tools and potential drug leads [J].
Dutton, JL ;
Craik, DJ .
CURRENT MEDICINAL CHEMISTRY, 2001, 8 (04) :327-344
[10]   A novel conotoxin from Conus betulinus, κ-BtX, unique in cysteine pattern and in function as a specific BK channel modulator [J].
Fan, CX ;
Chen, XK ;
Zhang, C ;
Wang, LX ;
Duan, KL ;
He, LL ;
Cao, Y ;
Liu, SY ;
Zhong, MN ;
Ulens, C ;
Tytgat, J ;
Chen, JS ;
Chi, CW ;
Zhou, Z .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (15) :12624-12633