نتایج جستجو برای: terfenadine

تعداد نتایج: 282  

Journal: :Mediators of Inflammation 1995
Marianela de Azevedo

Levocabastine is a new H(1)-receptor antagonist specifically developed for the topical treatment of seasonal allergic rhinoconjunctivitis. Clinical experience to date clearly demonstrates that levocabastine eye drops and nasal spray are effective and well tolerated for the treatment of this allergic disorder. Analysis of data from a number of comparative trials reveals that topical levocabastin...

Journal: :Journal of pharmacological and toxicological methods 2010
Shengde Peng Antonio E Lacerda Glenn E Kirsch Arthur M Brown Andrew Bruening-Wright

INTRODUCTION The cardiac action potential (CAP) of stem cell-derived human cardiomyocytes (SC-hCMs) is potentially the most powerful preclinical biomarker for cardiac safety and efficacy in humans. Our experiments tested this hypothesis by examining the CAP and relevant pharmacology of these cells. METHODS The electrophysiological and pharmacological profiles of SC-hCMs were compared to rabbi...

Journal: :Journal of pharmacological and toxicological methods 2015
Keiichi Asakura Seiji Hayashi Atsuko Ojima Tomohiko Taniguchi Norimasa Miyamoto Chiaki Nakamori Chiho Nagasawa Tetsuo Kitamura Tomoharu Osada Yayoi Honda Chieko Kasai Hiroyuki Ando Yasunari Kanda Yuko Sekino Kohei Sawada

INTRODUCTION Multi-electrode array (MEA) systems and human induced pluripotent stem (iPS) cell-derived cardiomyocytes are frequently used to characterize the electrophysiological effects of drug candidates for the prediction of QT prolongation and proarrhythmic potential. However, the optimal experimental conditions for obtaining reliable experimental data, such as high-pass filter (HPF) freque...

Journal: :The Journal of pharmacology and experimental therapeutics 1997
C M Ko I Ducic J Fan Y M Shuba M Morad

Nonsedating H1 receptor (H1-R) antagonists exert variable effects on QT interval, most likely mediated through modulation of cardiac K+ channels. We examined the effects of a novel H1-R antagonist, ebastine, on a family of K+ currents in isolated rat and guinea pig ventricular cardiomyocytes as well as on HERG-induced rapidly delayed rectifier K+ current (I(Kr)) in Xenopus laevis oocytes. The e...

Journal: :Antimicrobial agents and chemotherapy 2013
Anna C Jacobs Louis Didone Jennielle Jobson Madeline K Sofia Damian Krysan Paul M Dunman

Adenylate kinase (AK) is a ubiquitous intracellular enzyme that is released into the extracellular space upon cell lysis. We have shown that AK release serves as a useful reporter of bactericidal agent activity and can be exploited for antimicrobial screening purposes. The AK assay exhibits improved sensitivity over that of growth-based assays and can detect agents that are active against bacte...

Journal: :American journal of physiology. Cell physiology 2008
Heather Francis Shannon Glaser Sharon Demorrow Eugenio Gaudio Yoshiyuki Ueno Julie Venter David Dostal Paolo Onori Antonio Franchitto Marco Marzioni Shelley Vaculin Bradley Vaculin Khurshed Katki Monique Stutes Jennifer Savage Gianfranco Alpini

Cholangiopathies are characterized by the heterogeneous proliferation of different-sized cholangiocytes. Large cholangiocytes proliferate by a cAMP-dependent mechanism. The function of small cholangiocytes may depend on the activation of inositol trisphosphate (IP(3))/Ca(2+)-dependent signaling pathways; however, data supporting this speculation are lacking. Four histamine receptors exist (HRH1...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2010
Keiko Maekawa Noriko Harakawa Takuya Yoshimura Su-Ryang Kim Yoshiyuki Fujimura Fumika Aohara Kimie Sai Noriko Katori Masahiro Tohkin Mikihiko Naito Ryuichi Hasegawa Haruhiro Okuda Jun-ichi Sawada Takuro Niwa Yoshiro Saito

CYP3A4, the major form of cytochrome P450 (P450) expressed in the adult human liver, is involved in the metabolism of approximately 50% of commonly prescribed drugs. Several genetic polymorphisms in CYP3A4 are known to affect its catalytic activity and to contribute in part to interindividual differences in the pharmacokinetics and pharmacodynamics of CYP3A4 substrate drugs. In this study, cata...

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