نتایج جستجو برای: naftopidil

تعداد نتایج: 104  

Journal: :Iryo Yakugaku (Japanese Journal of Pharmaceutical Health Care and Sciences) 2005

2011
Takaki Mizusawa Noboru Hara Kenji Obara Etsuko Isahaya Yuki Nakagawa Kota Takahashi

Objectives. To examine the feature of men who benefit from dose escalation of naftopidil for lower urinary tract symptoms (LUTSs). Methods. Based on the IPSS, men reporting LUTS were prospectively studied using 50 mg/day of naftopidil for the first 4 weeks; satisfied patients continued its 50 mg/day (n = 11), and those reporting unsatisfactory improvement received its 75 mg/day (n = 35) for the...

2017
Tsuyoshi Hattori Philippe Lluel Céline Rouget Moèz Rekik Mitsuharu Yoshiyama

PURPOSE The aim of this study was to assess the potential involvement of a specific subtype of 5-hydroxytryptamine (5-HT), 5HT2 receptors in neurally-induced contractions of the human detrusor. METHODS Contractile responses to electrical field stimulation (EFS) were examined in human isolated urinary bladder muscle strips. The potentiation of EFS-induced detrusor contraction was examined by a...

2014
Nobumichi Tanaka Kazumasa Torimoto Isao Asakawa Makito Miyake Satoshi Anai Akihide Hirayama Masatoshi Hasegawa Noboru Konishi Kiyohide Fujimoto

BACKGROUND To evaluate the effect of two different alpha-1 adrenoceptor antagonists on lower urinary tract symptoms in patients who underwent LDR-brachytherapy. METHODS A total of 141 patients who had been clinically diagnosed with localized prostate cancer and underwent LDR-brachytherapy were enrolled. Patients were randomized and allocated to two groups (silodosin 8 mg vs. naftopidil 75 mg)...

Journal: :Pharmacology 2013
Takeshi Kanno Akito Tanaka Tadashi Shimizu Takashi Nakano Tomoyuki Nishizaki

The aim of the present study was to assess the anticancer effect of several naftopidil analogues on human malignant mesothelioma cell lines NCI-H28, NCI-H2052, NCI-H2452, and MSTO-211H, human lung cancer cell lines A549, SBC-3, and Lu-65, human hepatoma cell lines HepG2 and HuH-7, human gastric cancer cell lines MKN-28 and MKN-45, and human bladder cancer cell lines 253J, 5637, KK-47, TCCSUP, T...

Journal: :The Journal of urology 2012
Saori Nishijima Kimio Sugaya Katsumi Kadekawa Katsuhiro Ashitomi Hideyuki Yamamoto

PURPOSE We assessed the influence of the medial frontal lobe on micturition after chemical stimulation. We also examined the relation between the medial frontal lobe and the rostral pontine reticular formation, which has a strong inhibitory effect on micturition. MATERIALS AND METHODS A total of 35 female rats underwent continuous cystometry. Bladder activity changes were examined after physi...

Journal: :iranian journal of analytical chemistry 2015
alankar shrivastava

benign prostatic hyperplasia generally affects males above fourty years of age and has significant effect in overall quality of life (qol). this is one of the cause of millions of dollors in healthcare expenditure. alpha one adrenoreceptor blockers are frequently used for the benign prostatic enlargement because of their significant effect on storage and voiding symptoms, qol, flow rate and pos...

2014
Yoshiko Kaku Hisao Nagaya Ayako Tsuchiya Takeshi Kanno Akinobu Gotoh Akito Tanaka Tadashi Shimizu Syuhei Nakao Chiharu Tabata Takashi Nakano Tomoyuki Nishizaki

The newly synthesized naftopidil analogue HUHS1015 reduced cell viability in malignant pleural mesothelioma cell lines MSTO-211H, NCI-H28, NCI-H2052, and NCI-H2452, with the potential greater than that for the anticancer drugs paclitaxel or cisplatin at concentrations higher than 30 μM. HUHS1015 induced both necrosis and apoptosis of MSTO-211H and NCI-H2052 cells. HUHS1015 upregulated expressio...

Journal: :Biological & pharmaceutical bulletin 2012
Shuichi Sato Toshiki Hatanaka Hironori Yuyama Masashi Ukai Yukiko Noguchi Akiyoshi Ohtake Katsunari Taguchi Masao Sasamata Keiji Miyata

We determined the binding affinity of tamsulosin, a selective α(1)-adrenoceptor antagonist, for human α(1)-adrenoceptor subtypes in comparison with those of other α(1)-adrenoceptor antagonists including silodosin, prazosin, 5-methylurapidil, terazosin, alfuzosin, nafopidil, urapidil and BMY7378. The association and dissociation kinetics of [(3)H]tamsulosin for recombinant human α(1)-adrenocepto...

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