نتایج جستجو برای: spider venoms

تعداد نتایج: 14870  

Journal: :Neuroscience Letters 2013
Erica A. Gelfuso José L. Liberato Alexandra O.S. Cunha Márcia R. Mortari Renê O. Beleboni Norberto P. Lopes Wagner F. dos Santos

The aims of the present work were to investigate the effects of the repeated administration of Parawixin2 (2-amino-5-ureidopentanamide; formerly FrPbAII), a novel GABA and glycine uptake inhibitor, in rats submitted to PTZ-induced kindling. Wistar rats were randomly divided in groups (n=6-8) for different treatments. Systemic injections of PTZ were administered every 48 h in the dose of 33 mg/k...

2017
Jennifer R. Deuis Zoltan Dekan Joshua S. Wingerd Jennifer J. Smith Nehan R. Munasinghe Rebecca F. Bhola Wendy L. Imlach Volker Herzig David A. Armstrong K. Johan Rosengren Frank Bosmans Stephen G. Waxman Sulayman D. Dib-Hajj Pierre Escoubas Michael S. Minett Macdonald J. Christie Glenn F. King Paul F. Alewood Richard J. Lewis John N. Wood Irina Vetter

Human genetic studies have implicated the voltage-gated sodium channel NaV1.7 as a therapeutic target for the treatment of pain. A novel peptide, μ-theraphotoxin-Pn3a, isolated from venom of the tarantula Pamphobeteus nigricolor, potently inhibits NaV1.7 (IC50 0.9 nM) with at least 40-1000-fold selectivity over all other NaV subtypes. Despite on-target activity in small-diameter dorsal root gan...

Journal: :Molecular pharmacology 2015
Julie K Klint Yanni K-Y Chin Mehdi Mobli

Many spider-venom peptides are known to modulate the activity of the voltage-gated sodium (NaV) subtype 1.7 (NaV1.7) channel, which has emerged as a promising analgesic target. In particular, a class of spider-venom peptides (NaSpTx1) has been found to potently inhibit NaV1.7 (nanomolar IC50), and has been shown to produce analgesic effects in animals. However, one member of this family [µ-TRTX...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1978
M C Tzeng R S Cohen P Siekevitz

The effect of alpha-latrotoxin on cerebral cortex slices was studied by both biochemical and morphological methods. This toxin greatly stimulates the release of preloaded gamma-amino[3H]butyric acid from cortex slices. The response increases linearly with dose. The release is not dependent on the presence of extracellular Ca2+, and therefore it is not mediated by the release of other transmitte...

Journal: :Toxicon : official journal of the International Society on Toxinology 2004
Natalie G Lumsden Bryan G Fry R Manjunatha Kini Wayne C Hodgson

In this study, venoms from species in the Colubrinae, Homalopsinae, Natricinae, Pseudoxyrhophiinae and Psammophiinae snake families were assayed for activity in the chick biventer cervicis skeletal nerve muscle preparation. Boiga dendrophila, Boiga cynodon, Boiga dendrophila gemincincta, Boiga drapiezii, Boiga irregularis, Boiga nigriceps and Telescopus dhara venoms (10 microg/ml) displayed pos...

2012
Rong Chen Anna Robinson Shin-Ho Chung

Hanatoxin 1 (HaTx1) is a polypeptide toxin isolated from spider venoms. HaTx1 inhibits the voltage-gated potassium channel kv2.1 potently with nanomolar affinities. Its receptor site has been shown to contain the S3b-S4a paddle of the voltage sensor (VS). Here, the binding of HaTx1 to the VSs of human Kv2.1 in the open and resting states are examined using a molecular docking method and molecul...

Journal: :Molecular biology and evolution 2009
Greta J Binford Melissa R Bodner Matthew H J Cordes Katherine L Baldwin Melody R Rynerson Scott N Burns Pamela A Zobel-Thropp

The venom enzyme sphingomyelinase D (SMase D) in the spider family Sicariidae (brown or fiddleback spiders [Loxosceles] and six-eyed sand spiders [Sicarius]) causes dermonecrosis in mammals. SMase D is in a gene family with multiple venom-expressed members that vary in functional specificity. We analyze molecular evolution of this family and variation in SMase D activity among crude venoms usin...

Journal: :Molecular pharmacology 2006
Frank Bosmans Lachlan Rash Shunyi Zhu Sylvie Diochot Michel Lazdunski Pierre Escoubas Jan Tytgat

Four novel peptide toxins that act on voltage-gated sodium channels have been isolated from tarantula venoms: ceratotoxins 1, 2, and 3 (CcoTx1, CcoTx2, and CcoTx3) from Ceratogyrus cornuatus and phrixotoxin 3 (PaurTx3) from Phrixotrichus auratus. The pharmacological profiles of these new toxins were characterized by electrophysiological measurements on six cloned voltage-gated sodium channel su...

Journal: :The Journal of Cell Biology 1972
B. Ceccarelli W. P. Hurlbut A. Mauro

Curarized cutaneous pectoris nerve muscle preparations from frogs were subjected to prolonged indirect stimulation at 2/sec while recording from end plate regions. At the ends of the periods of stimulation, the curare was removed and the preparations were fixed for electron microscopy or treated with black widow spider venom to determine the degree to which their stores of transmitter had been ...

2015
Chun Yuen Chow Ben Cristofori-Armstrong Eivind A. B. Undheim Glenn F. King Lachlan D. Rash Jean-Marc Sabatier

Voltage-gated sodium (NaV) channels are responsible for propagating action potentials in excitable cells. NaV1.7 plays a crucial role in the human pain signalling pathway and it is an important therapeutic target for treatment of chronic pain. Numerous spider venom peptides have been shown to modulate the activity of NaV channels and these peptides represent a rich source of research tools and ...

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