Journal of Pharmacological Sciences

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LYG-202, a Newly Synthesized Flavonoid, Exhibits Potent Anti-angiogenic Activity In Vitro and In Vivo
Journal of Pharmacological Sciences - Tập 112 - Trang 37-45 - 2010
Yan Chen, Na Lu, Yun Ling, Ling Wang, Qidong You, Zhiyu Li, Qinglong Guo
Antiproliferative Effect of Echinacoside on Rat Pulmonary Artery Smooth Muscle Cells Under Hypoxia
Journal of Pharmacological Sciences - Tập 126 - Trang 155-163 - 2014
Xiang-Yun Gai, Feng Tang, Jing Ma, Ke-Wu Zeng, Sheng-Lan Wang, Ya-Ping Wang, Ta-Na Wuren, Dian-Xiang Lu, Yi Zhou, Ri-Li Ge
Oxazolone-Induced Colitis in BALB/C Mice: a New Method to Evaluate the Efficacy of Therapeutic Agents for Ulcerative Colitis
Journal of Pharmacological Sciences - Tập 96 - Trang 307-313 - 2004
Ryotaro Kojima, Satoko Kuroda, Tomiko Ohkishi, Koichi Nakamaru, Shigeki Hatakeyama
Inhibition of α 1E Ca2+ Channels by Carbonic Anhydrase Inhibitors
Journal of Pharmacological Sciences - Tập 95 - Trang 240 - 2004
Nicolle C.L. McNaughton, Andrew Randall, Ceri H. Davies
We examined if a range of carbonic anhydrase inhibitors (CAIs) interacted with the high-voltage activated voltage-sensitive calcium channels (VSCCs) encoded by the human α 1E subunit. Whole-cell recordings were made from HEK293 cells stably expressing human α 1E β 3-mediated calcium channels. SNX-482 (an α 1E inhibitor) blocked α 1E-mediated VSCCs with an IC50 close to 10 nM. The anticonvulsant CAI ethoxyzolamide also inhibited these currents, with an IC50 close to 1 μM, and produced an accompanying 20-mV hyperpolarizing shift in the steady-state inactivation profile. Other structurally diverse CAIs (e.g., acetazolamide and benzolamide) produced approximately 30 – 40% inhibition of α 1E β 3-mediated Ca2+ currents at 10 μM. Topiramate (10 μM), an anticonvulsant with CAI activity, inhibited these currents by 68 ± 7%. This off-target activity of CAIs at VSCCs may contribute to some of the effects they produce both in vitro and in vivo.
#voltage-sensitive calcium channel #carbonic anhydrase inhibitor #ethoxyzolamide #human Ca2+ channel subunit α 1E #human recombinant
Contribution of TRPV1 Receptor^|^ndash;Expressing Fibers to Spinal Ventral Root After-Discharges and Mechanical Hyperalgesia in a Spared Nerve Injury (SNI) Rat Model
Journal of Pharmacological Sciences - Tập 121 - Trang 9-16 - 2013
Shohei Yamamoto, Masahiro Ohsawa, Hideki Ono
Involvement of 5-HT2A receptor hyperfunction in the anxiety-like behavior induced by doxorubicin and cyclophosphamide combination treatment in rats
Journal of Pharmacological Sciences - Tập 138 - Trang 192-197 - 2018
Yuka Nakamura, Yoshihisa Kitamura, Yusuke Sumiyoshi, Nanami Naito, Shiho Kan, Soichiro Ushio, Ikuko Miyazaki, Masato Asanuma, Toshiaki Sendo
Impairment of endothelium-dependent vasodilator function of retinal blood vessels in adult rats with a history of retinopathy of prematurity
Journal of Pharmacological Sciences - Tập 146 - Trang 233-243 - 2021
Asami Mori, Daiki Sumida, Ryo Kondo, Ayuki Nakano, Shiho Arima, Daiki Asano, Akane Morita, Kenji Sakamoto, Tohru Nagamitsu, Tsutomu Nakahara
Lactucin & Lactucopicrin ameliorates FFA-induced steatosis in HepG2 cells via modulating lipid metabolism
Journal of Pharmacological Sciences - Tập 150 - Trang 110-122 - 2022
Yilizere Aibaidula, Mutalifu Aimaiti, Huiwen Tan, Bingting Chen, Jian Yang, Xiaoli Ma
Protective Effect of Prostaglandin EP4-Receptor Agonist on Anti-glomerular Basement Membrane Antibody-Associated Nephritis
Journal of Pharmacological Sciences - Tập 102 - Trang 182-188 - 2006
Tadashi Nagamatsu, Hirohito Imai, Michiyo Yokoi, Tsutomu Nishiyama, Yasushi Hirasawa, Toshiyuki Nagao, Yoshio Suzuki
The effects of rabeprazole on metformin pharmacokinetics and pharmacodynamics in Chinese healthy volunteers
Journal of Pharmacological Sciences - Tập 132 - Trang 244-248 - 2016
Guojing Liu, Jiagen Wen, Dong Guo, Zhenmin Wang, Xiaolei Hu, Jie Tang, Zhaoqian Liu, Honghao Zhou, Wei Zhang
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