Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.4161/chan.21628 http://scihub22266oqcxt.onion/10.4161/chan.21628 22922232!3508775!22922232     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=22922232&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215       Channels+(Austin) 2012 ; 6 (5): 362-9 Nephropedia Template TP {{tp|p=22922232|t=2012. 2-aminoethyl diphenyl borinate (2-APB) inhibits TRPM7 channels through an intracellular acidification mechanism |pdf=|usr=}}{{22922232}} gab.com Text 2-aminoethyl diphenyl borinate (2-APB) inhibits TRPM7 channels through an intracellular acidification mechanism JO: Channels (Austin) http://www.kidney.de/pget.php?&tw=1&pmid=22922232 #FOAvip 2-APB is a widely used compound in ion channel research. It affects numerous channels including inositol 1,4,5-trisphosphate receptors, store-operated calcium channels and TRP channels, TRPV3 and TRPM7 among them. A characteristic property of TRPM7 channels is their sensitivity to intracellular Mg ( 2+) and pH. Using patch clamp electrophysiology we find that in Jurkat T lymphocytes, 100-300 microM extracellular 2-APB reversibly inhibits TRPM7 channels when internal HEPES concentration is low (1 mM). Increasing the concentration to 140 mM abolishes the 2-APB effect. Using single-cell fluorescence pH video imaging, we show that at concentrations of 100 microM and higher, 2-APB potently acidifies the cytoplasm. We conclude that TRPM7 sensitivity to 2-APB is not direct but rather, can be explained by cytoplasmic acidification and a resulting channel inhibition. Twit Text FOAVip 2-aminoethyl diphenyl borinate (2-APB) inhibits TRPM7 channels through an intracellular acidification mechanism ????Channels (Austin) http://www.kidney.de/pget.php?&tw=1&pmid=22922232 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=22922232 #FOAvip English Wikipedia <ref>{{Cite pmid|22922232}}</ref> 2-aminoethyl diphenyl borinate (2-APB) inhibits TRPM7 channels through an intracellular acidification mechanism #MMPMID22922232 Chokshi R; Fruasaha P; Kozak JA Channels (Austin) 2012[Sep]; 6 (5): 362-9 PMID22922232show ga 2-APB is a widely used compound in ion channel research. It affects numerous channels including inositol 1,4,5-trisphosphate receptors, store-operated calcium channels and TRP channels, TRPV3 and TRPM7 among them. A characteristic property of TRPM7 channels is their sensitivity to intracellular Mg ( 2+) and pH. Using patch clamp electrophysiology we find that in Jurkat T lymphocytes, 100-300 microM extracellular 2-APB reversibly inhibits TRPM7 channels when internal HEPES concentration is low (1 mM). Increasing the concentration to 140 mM abolishes the 2-APB effect. Using single-cell fluorescence pH video imaging, we show that at concentrations of 100 microM and higher, 2-APB potently acidifies the cytoplasm. We conclude that TRPM7 sensitivity to 2-APB is not direct but rather, can be explained by cytoplasmic acidification and a resulting channel inhibition. |Boron Compounds/*pharmacology[MESH] |Humans[MESH] |Hydrogen-Ion Concentration[MESH] |Ion Channel Gating/drug effects[MESH] |Jurkat Cells[MESH] |Magnesium/metabolism[MESH] |Patch-Clamp Techniques[MESH] |Protein Serine-Threonine Kinases[MESH]2-aminoethyl diphenyl borinate (2-APB) inhibits TRPM7 channels through(epmc).pdf DeepDyve Pubget Overpricing