Kazuaki Kuroda
Nihon University
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Featured researches published by Kazuaki Kuroda.
Folia Endocrinologica Japonica | 1989
Motohisa Ishizaki; Kazuaki Kuroda; Nagao Kajiwara
Histamine H2-receptor antagonists administered into the central nervous system have been shown to increase arterial pressure (AP) in anaesthetized animals (Paakkari et al., 1982). Few studies have been reported on the effects of centrally administered cimetidine (CIM), one of the histamine H2-receptor antagonists, in conscious animals. However, the mechanism of the pressor action of histamine H2-receptor antagonists remains unclear. The present study was designed to investigate the hemodynamic effects of intracerebroventricular (i.c.v.) CIM and the interaction between the sympathetic nervous system and histamine receptor system in conscious rats. Male Wistar rats weighing 200 gr were prepared for the experiment under a conscious and minimally restricted state. Five micrograms of i.c.v. saline (SAL-ICV group, n = 5) did not produce significant changes in mean arterial pressure (MAP) or heart rate (HR) (MAP from 85.6 +/- 3.4 to 86.0 +/- 4.3 mmHg and HR from 395.0 +/- 13.9 to 395.2 +/- 8.2 bpm, respectively). Twenty micrograms of i.c.v. phenoxybenzamine (POB-ICV group, n = 6) decreased MAP from 95.8 +/- 4.1 to 85.2 +/- 3.1 mmHg, -10.7 +/- 2.2 mmHg as delta MAP, and increased HR from 392.5 +/- 8.5 to 435.3 +/- 13.9 bpm, +42.8 +/- 6.8 bpm as delta HR. Two-hundred micrograms of intravenous (i.v.) POB (POB-IV group, n = 5) also decreased MAP from 96.0 +/- 4.3 to 71.0 +/- 5.1 mmHg, -25.0 +/- 2.7 mmHg as delta MAP, and increased HR from 395.8 +/- 10.5 to 473.0 +/- 12.4 bpm, +77.2 +/- 7.6 bpm as delta HR. The changes in MAP and HR were much greater in the POB-IV group than those in the other two groups. The subsequent i.c.v. administration of 250 micrograms of CIM induced an increase in MAP (+19.4 +/- 1.7 mmHg as delta MAP) and a decrease in HR (-36.4 +/- 3.1 bpm as delta HR) in the SAL-ICV group, which continued for at least 30 minutes producing peak effects 2 minutes after i.c.v. administration of CIM. However, an elevation of MAP caused by i.c.v. CIM was much more inhibited in the POB-ICV group than in the POB-IV group (+2.5 +/- 0.7 mmHg as delta MAP in the POB-ICV group and +5.0 +/- 1.3 mmHg as delta MAP in the POB-IV group, respectively).(ABSTRACT TRUNCATED AT 400 WORDS)
Artificial Organs | 1982
Genjiro Kimura; Makoto Satani; Schunichi Kojima; Kazuaki Kuroda; Keiichi Itoh; Masao Ikeda
Japanese Circulation Journal-english Edition | 1981
Masayuki Tsuchiya; Shunichi Kojima; Masahiro Nakagawa; Akira Sakaguchi; Takashi Natsume; Genjiro Kimura; Kazuaki Kuroda; Masanobu Uda; Noboru Sakamoto; Makoto Satani; Keiichi Ito; Masao Ikeda
Journal of Japanese Society for Dialysis Therapy | 1980
Genjiro Kimura; Kazuaki Kuroda; Shunichi Kojima; Makoto Satani; Akiko Irie; Kimiaki Kadono; Hideto Kushiro; Junzo Kodama
日大醫學雜誌 | 2002
Tomoyoshi Yokose; Toru Hino; Kazuaki Kuroda; Katsuo Kanmatsuse
Kampo Medicine | 2002
Tomoyoshi Yokose; Toru Hino; Kazuaki Kuroda; Yumi Sakurai; Hisako Yamamoto; Tsuguto Yoshizawa; Tsunehide Oka; Katsuo Kanmatsuse
Japanese Heart Journal | 1993
Hiroshi Shirai; Yuichi Sato; Kazuaki Kuroda; Yasuhiro Akamine; Tatsuharu Sato; Masatsugu Fujii; Shigeru Wakayama; Masaaki Koizumi; Katsuo Kanmatsuse; Nagao Kajiwara
Japanese Circulation Journal-english Edition | 1993
Yasuhiro Akamine; Yuichi Sato; Kazuaki Kuroda; Hiroshi Shirai; Masatsugu Fujii; Shigeru Wakayama; Masaaki Koizumi; Hisako Okubo; Yumi Sakurai; Tsuguto Yoshizawa; Nagao Kajiwara; Katsuo Kanmatsuse
Japanese Circulation Journal-english Edition | 1990
Tatsuharu Sato; Yuichi Sato; Takashi Sasaki; Kazuaki Kuroda; Haruka Kammatsuse; Kazuhige Tsujikawa; Takatomo Kikuchi; Sachiko Ogawa; Hiroshi Shirai; Masafumi Furusaka; Yasuhiro Akamine; Masatsugu Fujii; Nagao Kajiwara
Japanese Circulation Journal-english Edition | 1989
Kazuaki Kuroda; Takashi Sasaki; Haruka Kamimatsuse; Kazushige Tsujikawa; Shunichi Yabuki; Sachiko Ogawa; Masafumi Furusawa; Hiroshi Shirai; Yasuhiro Akamine; Tatsuharu Satoh; Nagao Kajiwara