Inhibitory actions of cilostazol on electrical responses of smooth muscle isolated from the guinea-pig stomach antrum
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概要
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We have investigated the effects of cilostazol, a type III phosphodiesterase inhibitor, on the electrical responses of smooth muscle tissue isolated from the guinea-pig stomach antrum. Cilostazol (10^<-5> M) inhibited slow waves recorded from circular muscle cells, but did not significantly alter the pacemaker potentials and follower potentials recorded from myenteric interstitial cells and longitudinal muscle cells respectively. Slow potentials generated in isolated circular muscle bundles without attached myenteric interstitial cells were inhibited by cilostazol (>10^<-7> M), while all membrane activities were abolished by 10^<-5> M cilostazol. In circular muscle bundles, the input resistance of smooth muscle cells and the refractory period for the generation of slow potentials were not altered during the inhibition of spontaneous activity with cilostazol. While cilostazol at 10^<-7> and 10^<-6> M did not elevate the tissue content of cyclic AMP, at 10^<-5> M cyclic AMP was elevated by about 30%. A similar elevation was also produced by 10^<-7> M forskolin. The content of cyclic AMP was not significantly increased in preparations stimulated with 10^<-3> M caffeine. The potency for inhibiting slow waves was in the order caffeine (10^<-3> M) > forskolin (10^<-7> M) > cilostazol (10^<-5> M). The frequency of slow waves was decreased by caffeine or forskolin but not by cilostazol, while the duration was reduced by caffeine but not by cilostazol or forskolin. Follower potentials were modulated by caffeine and forskolin, but not by cilostazol: the duration was reduced by caffeine, the frequency was reduced by caffeine or forskolin, and the amplitude was not significantly altered by any of them. The results indicate that cilostazol has high selectivity in inhibiting the activity of circular muscle much more than that of longitudinal muscle or pacemaker cells, with no causal relation to the tissue content of cyclic AMP as appears to be the case for the inhibitory actions of caffeine and forskolin.
- 日本平滑筋学会の論文
著者
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Kobayashi Y
Department Of Gastroenterology And Metabolism Nagoya City University Graduate School Of Medical Scie
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SUZUKI Hikaru
Department of Physiology, Nagoya City University Medical School
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NAKAMURA Eri
Department of Physiology, Nagoya City University Medical School
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KITO Yoshihiko
Department of Physiology, Nagoya City University Medical School
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Kito Yoshihiko
Department Of Gastroenterology And Metabolism Nagoya City University Graduate School Of Medical Scie
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Hashimoto Ayako
Research Institute Of Pharmacological & Therapeutical Development Otsuka Pharmaceutical Co. Ltd.
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Suzuki H
Department Of Physiology Nagoya City University Medical School
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HASHITANI Hikaru
Department of Physiology, Nagoya City University Medical School
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MORI Toyoki
Research Institute of Pharmacological & Therapeutical Development, Otsuka Pharmaceutical Co., Ltd.
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Hashitani Hikaru
Department Of Physiology Nagoya City University Medical School
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Mori Toyoki
Research Institute Of Pharmacological & Therapeutical Development Otsuka Pharmaceutical Co. Ltd.
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Kobayashi Yoshinao
Department Of Gastroenterology And Hepatology Division Of Clinical Medicine And Biomedical Science I
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Suzuki Hikaru
Department Of Physiology Nagoya City University Medical School
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Suzuki Hikaru
Department Of Cell Physiology Nagoya City University Medical School
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Kamiya Yoshinobu
名古屋市立大学大学院医学研究科消化器・代謝内科学
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Hashitani Hikaru
Dep. Of Physiology Nagoya City Univ. Medical School
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Kito Y
Department Of Gastroenterology And Metabolism Nagoya City University Graduate School Of Medical Scie
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Suzuki Hikaru
Dep. Of Cell Physiology
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Nakamura Eri
Dep. Of Cell Physiology
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Nakamura Eri
Department Of Cell Physiology Nagoya City University Medical School
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Suzuki Hikaru
Department Of Cardiology Tokyo Women's Medical University
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Kuwabara Yoshiyuki
Department Of Oncology Immunology And Surgery Nagoya City University Graduate School Of Medical Scie
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Hashitani Hikaru
Department Of Cell Physiology Nagoya City University Medical School
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KITO Yoshihiko
Department of Cell Physiology, Nagoya City University Medical School
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