نتایج جستجو برای: coadministration

تعداد نتایج: 2844  

Journal: :Cardiovascular research 2010
Hiroshi Ohkawara Toshiyuki Ishibashi Shu-ichi Saitoh Nobutaka Inoue Koichi Sugimoto Masashi Kamioka Hironori Uekita Takashi Kaneshiro Katsuya Ando Yoh Takuwa Yukio Maruyama Yasuchika Takeishi

AIMS Small GTPases RhoA and Rac1 play crucial roles in endothelial dysfunction and reactive oxygen species (ROS) generation. We reported evidence that in thrombin-stimulated endothelial cells, rapid geranylgeranylation is an essential process for full activation of unprocessed RhoA, which is blocked by statin. In this study, we examined the effects of intravenous administration of pravastatin o...

2012
Leonid Kagan Donald E. Mager

Absorption of monoclonal antibodies (mAbs) after s.c. injection results from the interplay among several kinetic processes. The aims of this study were to investigate the absorption mechanisms of rituximab in rats by using slow s.c. infusion and coadministration with nonspecific IgG or hyaluronidase, and to evaluate the predictive performance of the pharmacokinetic model previously developed to...

Journal: :Neurology 2012
G L Birbeck J A French E Perucca D M Simpson H Fraimow J M George J F Okulicz D B Clifford H Hachad R H Levy

OBJECTIVE To develop guidelines for selection of antiepileptic drugs (AEDs) among people with HIV/AIDS. METHODS The literature was systematically reviewed to assess the global burden of relevant comorbid entities, to determine the number of patients who potentially utilize AEDs and antiretroviral agents (ARVs), and to address AED-ARV interactions. RESULTS AND RECOMMENDATIONS AED-ARV adminis...

2011
Girija Dasmahapatra Dmitry Lembersky Minkyeong P. Son Elisa Attkisson Paul Dent Richard I. Fisher Jonathan W. Friedberg Steven Grant

Interactions between the proteasome inhibitor carfilzomib and the histone deacetylase (HDAC) inhibitors vorinostat and SNDX-275 were examined in mantle cell lymphoma (MCL) cells in vitro and in vivo. Coadministration of very low, marginally toxic carfilzomib concentrations (e.g., 3–4 nmol/L) with minimally lethal vorinostat or SNDX-275 concentrations induced sharp increases in mitochondrial inj...

2014
Martha Kampp Nøhr Zia I Thale Birger Brodin Steen H Hansen René Holm Carsten Uhd Nielsen

Vigabatrin is an antiepileptic drug substance mainly used in pediatric treatment of infantile spasms. The main source of nutrition for infants is breast milk and/or infant formula. Our hypothesis was that infant formula may affect the intestinal absorption of vigabatrin. The aim was therefore to investigate the potential effect of coadministration of infant formula with vigabatrin on the oral a...

Journal: :Neuro-Signals 2014
Xiao-Peng Mei Yasushi Sakuma Cheng Xie Dan Wu Ichinyo Ho Junichiro Kotani Li-Xian Xu

Our previous study indicated that coadministration of tramadol and minocycline exerted synergistic effects on spinal nerve ligation (SNL)-induced neuropathic mechanical allodynia. However, the underlying mechanisms are still unclear. Recent reports indicated that spinal proinflammatory factor interleukin-1β (IL-1β) contributed to the development of neuropathic pain and the positive feedback com...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2016
Kenji Ikemura Yugo Hamada Chinatsu Kaya Tomoyuki Enokiya Yuichi Muraki Hiroki Nakahara Hajime Fujimoto Tetsu Kobayashi Takuya Iwamoto Masahiro Okuda

Pemetrexed, a multitargeted antifolate, is eliminated by tubular secretion via human organic anion transporter 3 (hOAT3). Although proton pump inhibitors (PPIs) are frequently used in cancer patients, the drug interaction between PPIs and pemetrexed remains to be clarified. In this study, we examined the drug interaction between pemetrexed and PPIs in hOAT3-expressing cultured cells, and retros...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2013
Leonid Kagan Donald E Mager

Absorption of monoclonal antibodies (mAbs) after s.c. injection results from the interplay among several kinetic processes. The aims of this study were to investigate the absorption mechanisms of rituximab in rats by using slow s.c. infusion and coadministration with nonspecific IgG or hyaluronidase, and to evaluate the predictive performance of the pharmacokinetic model previously developed to...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2000
K Komatsu K Ito Y Nakajima S i Kanamitsu S Imaoka Y Funae C E Green C A Tyson N Shimada Y Sugiyama

Drug-drug interactions between tolbutamide and sulfonamides have extensively been reported. We attempted to predict the in vivo interaction between tolbutamide and sulfonamides from the in vitro metabolic inhibition studies. The inhibition constant (K(i)) was derived from the inhibitory effects of eight sulfonamides (sulfaphenazole, sulfadiazine, sulfamethizole, sulfisoxazole, sulfamethoxazole,...

Journal: :Progress in neuro-psychopharmacology & biological psychiatry 2006
Takuya Masui Ichiro Kusumi Yoshito Takahashi Tsukasa Koyama

Perospirone is a serotonin 5-HT(2A) and dopamine D(2) receptor antagonist which originated in Japan. It has been shown that perospirone is metabolized to ID-15036 mainly by CYP3A4 based on an in vitro study. To investigate the metabolism of perospirone in humans, the authors measured the concentration of perospirone and ID-15036 after a single oral dose of perospirone (8 mg) in 10 healthy male ...

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