Akio Inui
University of Tokyo
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Publication
Featured researches published by Akio Inui.
Clinical and Experimental Pharmacology and Physiology | 2015
Yingxiao Li; Kai-Chun Cheng; Akihiro Asakawa; Haruka Amitani; Yoshiyuki Takimoto; Joshua Runtuwene; Akio Inui
Agmatine, an endogenous ligand of imidazoline receptors, is reported to exhibit anti‐hyperglycaemic and many other effects. It has been established that the imidazoline I3 receptor is involved in insulin secretion. The current study characterizes the role of the imidazoline I3 receptor in the protection of pancreatic islets. The activity effect of agmatine against on streptozotocin (STZ)‐induced (5 mmol/L) rat β cell apoptosis was examined by using ApoTox‐Glo triplex assay, live/dead cell double staining assay, flow cytometric analysis, and western blot. Imidazoline I3 receptors antagonist KU14R and the phospholipase C inhibitor named U73122 were treated in β cells to investigate the potential signalling pathways. The serum glucose and recovery of insulin secretion were measured in STZ‐treated rats after continuously injected agmatine. The apoptosis in rat β cells was reduced by agmatine in a dose‐dependent manner, cell viability was improved after treatment with agmatine and these effects were suppressed after the blockade of KU14R and U73122. Western blot analysis confirmed that agmatine could decrease caspase‐3 expression and increase the p‐BAD levels. In STZ‐treated rats, injection of agmatine for 4 weeks may significantly lower the serum glucose and recovery of insulin secretion. This improvement of pancreatic islets induced by agmatine was deleted by KU14R in vivo. Agmatine can activate the imidazoline I3 receptor linked with the phospholipase C pathway to induce cell protection against apoptosis induced by a low dose of STZ. This finding provides new insight into the prevention of early stage pancreatic islet damage.
Neuropsychiatry | 2017
Haruka Amitani; Robert A. Sloan; Nanami Sameshima; Koichi Yoneda; Marie Amitani; Akinori Morinaga; Yoshihiro Uto; Toshio Inui; Akio Inui; Akihiro Asakawa
Recently, immunotherapy has emerged as a new and appealing strategy for cancer treatment and various other acute and chronic diseases. Essential components of the natural immune system-phagocytic cells called macrophages-multiply in response to an infection in the body. The use of a macrophage activating therapy, such as macrophage activating factor (MAF), has extensive applications for treating numerous diseases by activating the natural macrophages of the body to stimulate the immune system. The aim of this review is to provide insight into the features and clinical efficacy of a new type of macrophage-activating factor derived from colostrum, called colostrum MAF.
Archive | 2002
Akio Inui; Akihiro Asakawa; Toshihiro Kaga
Handbook of Biologically Active Peptides (Second Edition) | 2013
Simona Perboni; Marzia Vignoni; Akio Inui
Archive | 2005
Akio Inui; Yoshiyuki Takimoto; Simona Perboni; Giovanni Mantovani
Archive | 2003
Akio Inui; Akihiro Asakawa
Archive | 2003
Masaaki Yoshikawa; Kuniko Takagi; Kousaka Ohinata; Akio Inui; Akihiro Asakawa; Shinji Kakudo
Archive | 2005
Noriko Kodama; Yukihito Murata; Akihiro Asakawa; Akio Inui; Masahiko Hayashi; Norio Sakai; Hiroaki Nanba
Archive | 2005
Masaaki Yoshikawa; Kuniko Takagi; Kousaku Ohinata; Akio Inui; Akihiro Asakawa; Shinji Kakudo
Archive | 2005
Shigeto Mizuno; Yoshinori Morita; Toshio Inui; Akihiro Asakawa; Naohiko Ueno; Takashi Ando; Haruki Kato; Mutsumi Uchida; Toshikazu Yoshikawa; Akio Inui