Paxilline |
| Katalog-Nr.GC11082 |
Blocker für hochleitfähige Ca2+-aktivierbare K+ (BKCa, KCa1.1) Kanäle
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 57186-25-1
Sample solution is provided at 25 µL, 10mM.
;)
,-1-7$$$37316672.jpg');)
;)
;)
$$$36806353.jpg');)
;33(7)%EF%BC%9A546-561$$$37156877.jpg');)
;)
;)
;)
%201124-1138.$$$35908550.jpg');)
%20766-780.$$$37100057.jpg');)
%20418-432.$$$36893736.jpg');)
%EF%BC%9A-240-255.$$$35108512.jpg');)
533-545$$$36543525.jpg');)
%201-13.$$$36600053.jpg');)
;)
Paxilline is a tremor-causing fungal alkaloid that can effectively inhibit high-conductance Ca2+-activated K+ (BK) channels, with IC50 of approximately 10nM and Ki=1.9nM[1]. Paxilline affects the dynamic balance of intracellular calcium ions and the transmission of electrical signals by blocking BK channels, and is used to explore the reaction and mechanism of BK channels in cellular processes[2]. Paxilline also inhibits muscle/endoplasmic reticulum Ca2+ ATPase, IC50 = 5-50µM[3].
In vitro, Paxilline (4µM) treated HT 22 cells for 18 h had significant cytoprotective effects against glutamate-induced toxicity, independent of BKCa channel activity and oxidative stress induced by glutamate treatment[4]. Paxilline (30µM) treatment of U251 MG, U87 MG, U343 and U251 N glioma cell lines can enhance the TRAIL sensitivity of cells and induce cell apoptosis [5].
In vivo, Paxilline (2.2 and 4.4 µg/kg) administered intraperitoneally to C57BL/6 mice could eliminate tonic-clonic seizures in mice and also reduce the duration and intensity of epileptic seizures[6]. Paxilline (3µg/kg) significantly alleviated thalidomide-induced synaptic and cognitive dysfunction in mice via intraperitoneal injection[7].
References:
[1] Zhou Y, et al. Paxilline inhibits BK channels by an almost exclusively closed-channel block mechanism[J]. Gen Physiol. 2014 Nov;144(5):415-40.
[2] Jackson-Weaver, O., Paredes, D.A., Gonzalez Bosc, L.V., et al. Intermittent hypoxia in rats increases myogenic tone through loss of hydrogen sulfide activation of large-conductance Ca2+-activated potassium channels.[J].Circulation Research 108(12), 2011:1439-1447 .
[3] Knaus H G, McManus O B, Lee S H, et al. Tremorgenic indole alkaloids potently inhibit smooth muscle high-conductance calcium-activated potassium channels. [J]Biochemistry, 1994, 33(19): 5819-5828.
[4] Szewczyk K A .Glutamate-induced cell death in HT22 mouse hippocampal cells is attenuated by paxilline, a BK channel inhibitor[J].Mitochondrion, 2012.
[5]Kang Y J , Kim I Y , Kim E H ,et al.Paxilline enhances TRAIL-mediated apoptosis of glioma cells via modulation of c-FLIP, survivin and DR5[J].Experimental & Molecular Medicine, 2011, 43(1):24.
[6]Sheehan JJ, et al. Anticonvulsant effects of the BK-channel antagonist paxilline. Epilepsia [J].2009. 50(4):711-20.
[7]Tae-Yong Choi, Seung-Hyun Lee, Soo-Jeong Kim, et al. BK channel blocker paxilline attenuates thalidomide-caused synaptic and cognitive dysfunctions in mice[J].Scientific Reports volume 8, 2018: 17653.
Average Rating: 5 (Based on Reviews and 29 reference(s) in Google Scholar.)
GLPBIO products are for RESEARCH USE ONLY. Please make sure your review or question is research based.
Required fields are marked with *