Motohiro Morioka

Dr. Motohiro Morioka

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Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Kiyoshi KikuchiKiyoshi Kikuchi
Kiyoshi Kikuchi
STSalunya Tancharoen
Salunya Tancharoen
NTNobuyuki Takeshige
Nobuyuki Takeshige
MYMunetake Yoshitomi
Munetake Yoshitomi
MMMotohiro Morioka
Motohiro Morioka
ETEiichiro Tanaka
Eiichiro Tanaka
Edaravone was originally developed as a potent free radical scavenger, and has been widely used to treat acute ischemic stroke in Japan since 2001. Free radicals play an important role in the pathogenesis of a variety of diseases, such as cardiovascular diseases and stroke. Therefore, free radicals may be targets for therapeutic intervention in these diseases. Edaravone shows protective effects on ischemic insults and inflammation in the heart, vessel, and brain in experimental studies. As well as scavenging free radicals, edaravone has anti-apoptotic, anti-necrotic, and anti-cytokine effects in cardiovascular diseases and stroke. Edaravone has preventive effects on myocardial injury following ischemia and reperfusion in patients with acute myocardial infarction. Edaravone may represent a new therapeutic intervention for endothelial dysfunction in the setting of atherosclerosis, heart failure, diabetes, or hypertension, because these diseases result from oxidative stress and/or cytokine-induced apoptosis. This review evaluates the potential of edaravone for treatment of cardiovascular disease, and covers clinical and experimental studies conducted between 1984 and 2013. We propose that edaravone, which scavenges free radicals, may offer a novel option for treatment of cardiovascular diseases. However, additional clinical studies are necessary to verify the efficacy of edaravone.

31 August 2012 in Acta Neurochirurgica
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YKYasuyuki Kaku
Yasuyuki Kaku
MMMotohiro Morioka
Motohiro Morioka
YOYuki Ohmori
Yuki Ohmori
TKTakayuki Kawano
Takayuki Kawano
YKYutaka Kai
Yutaka Kai
JKJun-Ichi Kuratsu
Jun-Ichi Kuratsu

12 January 2022 in Neuro-Oncology Advances
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TIToshihiko Iuchi
Toshihiko Iuchi
AIAkihiro Inoue
Akihiro Inoue
YHYuichi Hirose
Yuichi Hirose
MMMotohiro Morioka
Motohiro Morioka
KHKeishi Horiguchi
Keishi Horiguchi
YSYukinori Sakata
Yukinori Sakata
Adjuvant treatment with Gliadel wafers may prolong overall survival (OS) for malignant glioma patients without increasing toxicity. In Japan, the long-term OS of these patients treated with Gliadel 7.7 mg implants has not been studied. We evaluated OS and prognostic factors that might affect OS in Japanese patients with malignant glioma who received the Gliadel 7.7 mg implant. This observational, long-term, postmarketing surveillance was an extension of a previous surveillance. Data were collected through case report forms at 2 and 3 years after Gliadel implant. Up to 8 Gliadel wafers (61.6 mg of carmustine) were placed over the tumor resection site. Primary endpoints were OS and prognostic factors that may influence OS. Among the 506 patients analyzed, 62.6% had newly diagnosed disease, and 37.4% had recurrent disease; 79.1% had glioblastoma histological type and 79.6% had World Health Organization Grade IV disease. Patients received a median of 8 wafers. The median OS was 18.0 months; OS rates were 39.8% and 31.5% at 2 and 3 years, respectively. Age ≥65 years (hazard ratio [HR]: 1.456; P = .002), lower resection rate (HR: 1.206; P < .001), recurrence (HR: 2.418; P < .001), and concomitant radiotherapy (HR: 0.588; P < .001) were identified as significant prognostic factors. This study confirmed the 2- and 3-year OS of Japanese malignant glioma patients with varied backgrounds after Gliadel implant. With a careful interpretation of indirect comparisons with previously reported data, the results suggest that prognosis could be improved with Gliadel implants. NCT02300506

Verified
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Kiyoshi KikuchiKiyoshi Kikuchi
Kiyoshi Kikuchi
HUHisaaki Uchikado
Hisaaki Uchikado
MMMotohiro Morioka
Motohiro Morioka
YMYoshinaka Murai
Yoshinaka Murai
ETEiichiro Tanaka
Eiichiro Tanaka
Stroke is an enormous public health problem with an imperative need for more effective therapies. In therapies for ischemic stroke, tissue plasminogen activators, antiplatelet agents and anticoagulants are used mainly for their antithrombotic effects. However, free radical scavengers, minocycline and growth factors have shown neuroprotective effects in the treatment of stroke, while antihypertensive drugs, lipid-lowering drugs and hypoglycemic drugs have shown beneficial effects for the prevention of stroke. In the present review, we evaluate the treatment and prevention of stroke in light of clinical studies and discuss new anti-stroke effects other than the main effects of drugs, focusing on optimal pharmacotherapy.

24 December 2015 in Journal of Stroke and Cerebrovascular Diseases
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YNYukihiko Nakamura
Yukihiko Nakamura
YSYasuo Sugita
Yasuo Sugita
SNShinji Nakashima
Shinji Nakashima
YOYousuke Okada
Yousuke Okada
MYMunetake Yoshitomi
Munetake Yoshitomi
KOKoichi Ohshima
Koichi Ohshima

1 January 2017 in Neurologia medico-chirurgica
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MMMotohiro Morioka
Motohiro Morioka
KOKimihiko Orito
Kimihiko Orito
The incidence of spontaneous intracerebral hematoma (SICH) is even now high worldwide, especially higher in Japan than in Western countries, despite the development of advances in blood pressure (BP) management and food/alcohol intake education. Although mortality and morbidity for SICH are high, some controversies remain regarding the appropriate acute phase of treatment. Recent studies have revealed that BP lowering treatment than 140 mmHg resulted in better outcomes. However the efficacy of surgical treatment for SICH has not been well established, with the exception of that for cerebellar SICH over 3 cm in diameter and life-saving procedures, although many randomized control studies and systematic reviews focused on surgical treatment have been reported. In this review, we summarize some issues and discuss strategies in development for the treatment of SICH.