Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2004-7-20
pubmed:abstractText
Because many studies rely upon detergents to solubilize lipophilic agents such as cannabinoid drugs, we examined the effect of commonly employed detergents on the function of the cloned alpha(7) subunit of the nicotinic ACh receptor. Homomeric alpha(7) receptors were expressed in Xenopus oocytes and the two-microelectrode voltage-clamp technique was used to assess their electrophysiological properties. The detergents Tween 80 and Triton X-100 reversibly inhibited ACh (100 microM)-induced inward currents in a concentration-dependent manner, with IC(50) values of 610 nM and 1.4 microM, respectively. The effects of these detergents were independent of membrane potential, and they were not mediated by endogenous Ca(2+)-dependent Cl(-) channels, since they were unaffected by intracellularly injected BAPTA, and recorded in Ca(2+)-free bathing solution containing 2 mM Ba(2+). Both detergents also decreased the maximal effect of ACh, without significantly affecting its EC(50), indicating a non-competitive interaction with the nACh alpha(7) receptors. In contrast to the effects of these detergents, we found that cholic acid (10 microM), DMSO (10 microM) and Tocrisol (0.01% v/v) did not cause a significant effect on nicotinic responses. In conclusion, we demonstrate that the detergents Tween 80 and Triton X-100 are potent inhibitors of neuronal nACh alpha(7) receptors expressed in Xenopus oocytes, and we suggest that studies utilizing these detergents to solubilize lipophilic drugs should be scrutinized for such effects.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/1,2-bis(2-aminophenoxy)ethane-N,N,N'..., http://linkedlifedata.com/resource/pubmed/chemical/Acetylcholine, http://linkedlifedata.com/resource/pubmed/chemical/Atropine, http://linkedlifedata.com/resource/pubmed/chemical/Barium, http://linkedlifedata.com/resource/pubmed/chemical/Chelating Agents, http://linkedlifedata.com/resource/pubmed/chemical/Detergents, http://linkedlifedata.com/resource/pubmed/chemical/Egtazic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Muscarinic Antagonists, http://linkedlifedata.com/resource/pubmed/chemical/Octoxynol, http://linkedlifedata.com/resource/pubmed/chemical/Polysorbates, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Complementary, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Nicotinic, http://linkedlifedata.com/resource/pubmed/chemical/alpha7 nicotinic acetylcholine...
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0165-0270
pubmed:author
pubmed:issnType
Print
pubmed:day
30
pubmed:volume
137
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
167-73
pubmed:dateRevised
2010-6-4
pubmed:meshHeading
pubmed-meshheading:15262057-Acetylcholine, pubmed-meshheading:15262057-Animals, pubmed-meshheading:15262057-Atropine, pubmed-meshheading:15262057-Barium, pubmed-meshheading:15262057-Chelating Agents, pubmed-meshheading:15262057-Chickens, pubmed-meshheading:15262057-Cloning, Molecular, pubmed-meshheading:15262057-Detergents, pubmed-meshheading:15262057-Dose-Response Relationship, Drug, pubmed-meshheading:15262057-Drug Interactions, pubmed-meshheading:15262057-Egtazic Acid, pubmed-meshheading:15262057-Female, pubmed-meshheading:15262057-Membrane Potentials, pubmed-meshheading:15262057-Muscarinic Antagonists, pubmed-meshheading:15262057-Neural Inhibition, pubmed-meshheading:15262057-Octoxynol, pubmed-meshheading:15262057-Oocytes, pubmed-meshheading:15262057-Patch-Clamp Techniques, pubmed-meshheading:15262057-Polysorbates, pubmed-meshheading:15262057-RNA, Complementary, pubmed-meshheading:15262057-Receptors, Nicotinic, pubmed-meshheading:15262057-Xenopus laevis
pubmed:year
2004
pubmed:articleTitle
The solubilizing detergents, Tween 80 and Triton X-100 non-competitively inhibit alpha 7-nicotinic acetylcholine receptor function in Xenopus oocytes.
pubmed:affiliation
National Institute on Drug Abuse, NIH/DHHS, Intramural Research Program, Cellular Neurobiology Branch, Cellular Neurophysiology Section, 5500 Nathan Shock Drive, Baltimore, MD 21224, USA.
pubmed:publicationType
Journal Article, Comparative Study