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18篇 您的检索式:作者名="Whiteaker J"
    题名 作者 年代 出处 被引量
1Integrated Pipe- line for Mass Spectrometry-Based Discovery and Confirmation of Biomarkers Demonstrated in a Mouse Model of Breast Cancer显示文摘Whiteaker J Zhang H Zhao L 2007J Proteome Res2007,6,:1
2^125I-α-Conotoxin MII identifies a novel nicotinic acetylcholine receptor population in mouse brain显示文摘Whiteaker P McIntosh J M Luo S 2000Mol Pharmacol2000,57,:1
3Antibody-based enrichment of peptides on magnetic beads for mass-spectrometry-based quantification of serum biomarkers显示文摘Whiteaker J Zhao L Zhang HY 2007Anal Biochem2007,362,:1
4Integrated pipeline for mass spectrometry-based discovery and confirmation of biomarkers demonstrated in a mouse model of breast cancer显示文摘Whiteaker J R Zhang H Zhao L 2007J Proteome Res2007,6,10:1
5A targeted proteomics-based pipeline for verification of biomarkers in plasma显示文摘Whiteaker JR Lin C Kennedy J 2011Nat Biotechnol2011,29,7:1
6A first approach to Web services for the national water information system显示文摘GOODALL J L HORSBURGH J S WHITEAKER T L 2008Environmental Modelling & Software2008,23,4:1
7Explaining packet de- lays under virtualization 显示文摘Whiteaker J Schneider F Teixeira R 2011Computer Communication Re-view2011,41,1:1
8Effects ofmeteorological conditions on aerosol composition and mixing statein bakersfield,CA 显示文摘Whiteaker J R Suess D T Prather K A 2002Environmental Science Technology2002,36,11:1
9Antibody-based enrichment of peptides on magnetic beads for mass-spectrometry-based quantification of serum biomarkers显示文摘WHITEAKER J R ZHAO L ZHANG H Y 2007Anal Biochem2007,362,1:1
10Pharmacological and immunochemical characterization of α2* nicotinic acetylcholine receptors (nAChRs) in mouse brain显示文摘Paul WHITEAKER Jennifer A WILKING Robert WB BROWN Robert J BRENNAN Allan C COLLINS Jon M LINDSTROM Jim BOULTER 2009Acta Pharmacologica Sinica2009,30,6:1
11Antibody-based enrichment of peptides on magnetic beads for mass-spectrometry- based quantification of serum biomarkers 显示文摘WHITEAKER J R ZHAO L ZHANG H Y 2007Anal Biochem2007,362,1:1
12Explaining Packet I)e- lays under Virtualization 显示文摘Whiteaker J Schneider F Teixeira R 2011Computer Communication Re- view2011,41,1:1
13Pharmacological and functional comparisons of α6/ α31β2β3-nAChRs and (α4β2-nAChRs heterologously expressed in the human epithelial SH-EP1 cell line显示文摘De-jie CHEN Fen-fei GAO Xiao-kuang MA Gang-gang SHI Yuan-bing HUANG Quang-xi SU Sterling SUD- WEEKS Ming GAO Turner DHARSHAUN Jason Brek EATON Yong-chang CHANG J Michael MClNTOSH Ronald J LUKAS Paul WHITEAKER Scott C STEFFENSEN Jie WU 2018Acta Pharmacologica Sinica2018,39,10:1
14A first approach to web services for the National Water Information System显示文摘Goodall J L Horsburgh J S Whiteaker T L 2008Environmental Modelling & Software2008,,:1
15A first approach to Web services for the national water information system显示文摘GOODALL J L HORSBURGII J S WHITEAKER T L 2008Environmental Modelling & Software2008,23,4:1
16A targeted proteomics-based pipeline for verification of biomarkers in plasma显示文摘Whiteaker J R Lin C Kennedy J 2011Nat Biotechnol2011,29,7:1
17Nicotinic acetylcholine receptor α7 subunits with a C2 cytoplasmic loop yellow fluorescent protein insertion form functional receptors显示文摘Teresa A MURRAY Qiang LIU Paul WHITEAKER Jie WU Ronald J LUKAS 2009Acta Pharmacologica Sinica2009,30,6:0
18Cocaine potently blocks neuronal α_(3)β_(4) nicotinic acetylcholine receptors in SH-SY5Y cells显示文摘Cocaine is one of the most abused illicit drugs worldwide.It is well known that the dopamine(DA)transporter is its major target;but cocaine also acts on other targets including nicotinic acetylcholine receptors(nAChRs).In this study,we investigated the effects of cocaine on a special subtype of neuronal nAChR,α3β4-nAChR expressed in native SH-SY5Y cells.α3β4-nAChR-mediated currents were recorded using whole-cell recordings.Drugs were applied using a computer-controlled U-tube drug perfusion system.We showed that bath application of nicotine induced inward currents in a concentration-dependent manner with an EC50 value of 20μM.Pre-treatment with cocaine concentration-dependently inhibited nicotine-induced current with an IC50 of 1.5μM.Kinetic analysis showed that cocaine acceleratedα3β4-nAChR desensitization,which caused a reduction of the amplitude of nicotine-induced currents.Co-application of nicotine and cocaine(1.5μM)depressed the maximum response on the nicotine concentration-response curve without changing the EC50 value,suggesting a non-competitive mechanism.The cocaine-induced inhibition of nicotine response exhibited both voltage-and use-dependence,suggesting an open-channel blocking mechanism.Furthermore,intracellular application of GDP-βS(via recording electrode)did not affect cocaine-induced inhibition,suggesting that cocaine did not alter receptor internalization.Moreover,intracellular application of cocaine(30μM)failed to alter the nicotine response.Finally,cocaine(1.5μM)was unable to inhibit the nicotine-induced inward current in heterologous expressedα6/α3β2β3-nAChRs andα4β2-nAChRs expressed in human SH-EP1 cells.Collectively,our results suggest that cocaine is a potent blocker for nativeα3β4-nAChRs expressed in SH-SY5Y cells.Ze-gang Ma Nan Jiang Yuan-bing Huang Xiao-kuang Ma Jason Brek Eaton Ming Gao Yong-chang Chang Ronald J Lukas Paul Whiteaker Janet Neisewander Jie Wu 2020Acta Pharmacologica Sinica2020,41,2:0
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