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Review of frequently used Kampo prescriptions: Part 4, Ninjin'yoeito 汉方常用方剂述评:第4部分:忍者约法
Pub Date : 2023-10-07 DOI: 10.1002/tkm2.1387
Shin Takayama, Seiwa Michihara, Yoko Kimura, Akinori Morinaga, Kyohei Miyakawa, Nobuhiko Tsushima, Kahori Otani, Atsuko Jinnai, Yuko Aso, Asako Okabayashi, Ryutaro Arita, Tatsuya Nogami, Akio Inui
Abstract Background The source of ninjin'yoeito (NYT) is considered the ‘Formulary of Bureau of Taiping People's Welfare Pharmacy’, written around 1241–52 AD. NYT is used to treat patients with chronic fatigue, malaise with qi deficiency, and exhaustion of all five parenchymatous viscera with difficulty in recovering. Key Findings NYT formula consists of 12 crude drugs. NYT extract for medical use is covered by the National Health Insurance system of Japan for convalescence after recovery from diseases, fatigue and malaise, anorexia, perspiration during sleep, cold limbs, and anemia. Studies have shown clinical effects of NYT: treatment of anemia, cancer treatment support, frailty, cognitive dysfunction, apathy, fatigue/malaise, anorexia, and lung diseases. Preclinical studies support clinical studies; activating ghrelin‐neuropeptide Y pathway‐mediated appetite‐enhancing effects, inhibiting muscle volume loss through the Akt/mTOR pathway‐mediated hyperphosphorylation of 4E‐BP1 and FoxO1‐mediated Atrogin‐1, suppressing the hypothalamic–pituitary–adrenal axis by downregulating the sympathetic‐adrenal‐medullary axis and GABA neurons for improving sociability, promoting recovery from skeletal muscle atrophy through the activation of PGC‐1α, hematopoiesis‐promoting effects, and increasing the number of immune cells in immunocompromised models. The incidence of adverse events of NYT was reported as 3.09 or 2.03%. The most significant adverse effects of NYT are gastrointestinal disorders. Conclusion Recently, NYT has been widely used to treat several symptoms and conditions under the National Health Insurance System of Japan. Clinical studies showed the efficacy of NYT to treat anemia, frailty, cognitive dysfunction, anorexia, apathy, and fatigue/malaise, as well as for long‐term cancer treatment support. The pharmacological mechanisms supporting its effects are also being reported.
摘要背景忍者约文(NYT)的来源被认为是写于公元1241 - 1252年左右的《太平民福药房局方书》。NYT用于治疗慢性疲劳,气虚不适,五实质脏腑衰竭,难以恢复的病人。NYT配方由12种生药组成。医疗用NYT提取物被纳入日本国民健康保险,用于从疾病、疲劳和不适、厌食症、睡眠出汗、四肢寒冷、贫血等疾病中恢复后的康复。研究表明,NYT的临床效果:治疗贫血、癌症治疗支持、虚弱、认知功能障碍、冷漠、疲劳/不适、厌食症和肺部疾病。临床前研究支持临床研究;激活ghrelin -神经肽Y通路介导的食欲增强作用,通过Akt/mTOR通路介导的4E - BP1和FoxO1介导的Atrogin - 1的过度磷酸化抑制肌肉体积损失,通过下调交感-肾上腺-髓质轴和GABA神经元来抑制下丘脑-垂体-肾上腺轴,以改善社交能力,通过激活PGC - 1α促进骨骼肌萎缩的恢复,促进造血作用。并增加免疫功能受损模型中的免疫细胞数量。NYT不良事件发生率分别为3.09和2.03%。NYT最显著的副作用是胃肠道紊乱。最近,NYT被广泛用于治疗日本国民健康保险制度下的几种症状和条件。临床研究表明,NYT治疗贫血、虚弱、认知功能障碍、厌食症、冷漠和疲劳/不适,以及长期癌症治疗支持。支持其作用的药理学机制也有报道。
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引用次数: 0
Three cases successfully treated with a combination of unkeito and boiogito for menopausal arthralgia 应用unketo联合biogito治疗绝经期关节痛3例
Pub Date : 2023-10-03 DOI: 10.1002/tkm2.1390
Daigo Taniguchi, Tatsuya Nogami, Noriko Miyatake, Toko Tsuruta, Makoto Arai
Traditional & Kampo MedicineEarly View LETTER TO THE EDITOR Three cases successfully treated with a combination of unkeito and boiogito for menopausal arthralgia Daigo Taniguchi, Daigo Taniguchi Department of Psychosomatic Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, JapanSearch for more papers by this authorTatsuya Nogami, Corresponding Author Tatsuya Nogami [email protected] orcid.org/0000-0002-9724-4356 Department of Kampo Medicine, Tokai University School of Medicine, Isehara, Japan Department of Kampo Medicine, Tomei Atsugi Clinic, Atsugi, Japan Correspondence Tatsuya Nogami, Department of Kampo Medicine, Tokai University School of Medicine, Isehara, Japan. Email: [email protected]Search for more papers by this authorNoriko Miyatake, Noriko Miyatake Department of Kampo Medicine, Tokai University School of Medicine, Isehara, JapanSearch for more papers by this authorToko Tsuruta, Toko Tsuruta Department of Obstetrics and Gynecology, Kofukyoritsu Hospital, Kofu, JapanSearch for more papers by this authorMakoto Arai, Makoto Arai Department of Kampo Medicine, Tokai University School of Medicine, Isehara, JapanSearch for more papers by this author Daigo Taniguchi, Daigo Taniguchi Department of Psychosomatic Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, JapanSearch for more papers by this authorTatsuya Nogami, Corresponding Author Tatsuya Nogami [email protected] orcid.org/0000-0002-9724-4356 Department of Kampo Medicine, Tokai University School of Medicine, Isehara, Japan Department of Kampo Medicine, Tomei Atsugi Clinic, Atsugi, Japan Correspondence Tatsuya Nogami, Department of Kampo Medicine, Tokai University School of Medicine, Isehara, Japan. Email: [email protected]Search for more papers by this authorNoriko Miyatake, Noriko Miyatake Department of Kampo Medicine, Tokai University School of Medicine, Isehara, JapanSearch for more papers by this authorToko Tsuruta, Toko Tsuruta Department of Obstetrics and Gynecology, Kofukyoritsu Hospital, Kofu, JapanSearch for more papers by this authorMakoto Arai, Makoto Arai Department of Kampo Medicine, Tokai University School of Medicine, Isehara, JapanSearch for more papers by this author First published: 03 October 2023 https://doi.org/10.1002/tkm2.1390Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1Magliano M. Menopausal arthralgia: fact or fiction. Maturitas. 2010; 67(1): 29–33. https://doi.org/10.1016/j.maturi
传统与北坡医学早期观点致编辑信联合unkeito和biogito成功治疗绝经期关节痛症3例Daigo Taniguchi, Daigo Taniguchi心身医学系,医学研究生院,九州大学,福冈,日本搜索作者的更多论文Tatsuya Nogami,通讯作者Tatsuya Nogami [email protected] orcid.org/0000-0002-9724-4356北坡医学系日本东海大学医学院,石原市,日本,大木市,tomeiatsugi诊所,汉方医学部,野上达也,日本,石原市,东海大学医学院,汉方医学部。电子邮件:[email protected]检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文日本搜索本作者谷口大吾的更多论文,谷口大吾的心身医学系,医学研究生院,九州大学,福冈,日本搜索本作者野上达也的更多论文,通讯作者野上达也[email protected] orcid.org/0000-0002-9724-4356日本东海大学医学院,石原,日本,大木富明诊所,日本大木,北坡医学系,通信野上达也,日本东海大学医学院汉布医学科,石原。电子邮件:[email protected]检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文检索本作者的更多论文日本搜索本文作者的更多论文首次发表:2023年10月3日https://doi.org/10.1002/tkm2.1390Read全文taboutpdf ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare给予accessShare全文accessShare全文accessShare全文accessShare请查看我们的使用条款和条件,并在下面的复选框中选择分享文章的全文版本。我已经阅读并接受了Wiley在线图书馆使用共享链接的条款和条件,请使用下面的链接与您的朋友和同事分享本文的全文版本。学习更多的知识。复制URL共享链接共享一个emailfacebooktwitterlinkedinreddit微信本文无摘要1Magliano M.绝经期关节痛:事实还是虚构。matuitas。2010;67(1): 29-33。https://doi.org/10.1016/j.maturitas.2010.04.009 2王晓明,王晓明,王晓明,等。黄酮类药物对卵巢功能亢进和功能低下女性卵泡刺激素、卵泡刺激素和雌二醇的影响。中华医学杂志2003;31(5): 763 - 771。https://doi.org/10.1142/S0192415X0300134X 3方凯,村上英,神田S, Shimono T,党AT,小野M,等。Unkeito通过Blimp1-Bcl6和NF-κB信号通路抑制rankl介导的破骨细胞生成,促进破骨细胞凋亡。中华生物医学杂志;2022;23日(14):7814。https://doi.org/10.3390/ijms23147814 4真岛君,王晓明,王晓明,王晓明。中药对膝关节积液性骨性关节炎的治疗作用。中华医学杂志;2012;4(1): 3。https://doi.org/10.1186/1758-2555-4-3早期视图记录在包含问题之前的在线版本参考信息
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引用次数: 0
Safety evaluation of continuous administration of a high dose of Valeriana fauriei root extract in mice and in humans through an open‐label study 通过一项开放标签研究,对小鼠和人类连续服用高剂量缬草根提取物的安全性进行评估
Pub Date : 2023-10-02 DOI: 10.1002/tkm2.1388
Misato Ota, Yuki Oiwa, Yasuhito Maki, Ichiro Utaka, Sachie Arima, Yoichi Matsuo, Toshiaki Makino, Shunsuke Nojiri
Abstract Aim This study aimed to clarify the safety of Valeriana fauriei root (VF) ethanol extract through in vivo and clinical trials. Methods Mice were divided into VF and control groups. They were given VF (4 g VF/kg/day) or the vehicle mixed in the powdered food for four weeks. Food consumption and body weight changes were evaluated, and blood biochemistry and organ weights were assessed on the last day. In addition, an open‐label study was conducted on healthy subjects who took VF capsules (10 g VF/body/day) for four weeks and were asked to report any changes in their physical condition. Physical, hematologic, blood biochemical examination and urinalysis were performed before, two weeks, and four weeks into the study. Results Food consumption and weight gain in mice did not differ between the VF and control groups, except for experimental error, and there were no particular differences in the weights of the brain, lung, heart, liver, spleen, and kidney. In mice, VF administration resulted in small but significant decreases in albumin in males and females, and total cholesterol and high‐density lipoprotein cholesterol in females only. These levels were unchanged, but daytime sleepiness was observed in humans. Conclusion Since there was little change in the experimental values at continuous high doses of VF at 10 g/day, it can be concluded that approximately one‐fifth of this dose (2 g VF/day) is less harmful. However, daytime sleepiness should be considered.
摘要目的通过体内试验和临床试验,阐明缬草根(VF)乙醇提取物的安全性。方法将小鼠分为VF组和对照组。分别给予VF (4 g VF/kg/天)或混合在粉状食品中的整车,连续4周。在最后一天评估食物消耗和体重变化,并评估血液生化和器官重量。此外,对健康受试者进行了一项开放标签研究,他们连续四周服用VF胶囊(10g VF/body/day),并被要求报告其身体状况的任何变化。研究开始前、2周和4周分别进行生理、血液学、血液生化检查和尿液分析。结果除实验误差外,VF组和对照组小鼠的食量和体重增加没有差异,脑、肺、心、肝、脾和肾的重量也没有特别的差异。在小鼠中,给药VF导致雄性和雌性小鼠白蛋白和总胆固醇和高密度脂蛋白胆固醇的小幅但显著下降。这些水平没有变化,但在人类中观察到白天嗜睡。结论:在10 g/天的连续高剂量VF下,实验值几乎没有变化,因此可以得出结论,大约五分之一的剂量(2 g VF/天)的危害较小。然而,白天的嗜睡应该被考虑在内。
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引用次数: 0
Preventive effect of a traditional Japanese Kampo medicine, shakuyakukanzoto, against neurotoxicity of FOLFOX plus bevacizumab used for metastatic colorectal cancer management: A single‐arm phase II study 日本传统汉布药shakuyakukanzoto对FOLFOX联合贝伐单抗用于转移性结直肠癌治疗的神经毒性的预防作用:单组II期研究
Pub Date : 2023-09-26 DOI: 10.1002/tkm2.1389
Hiroaki Takagi, Shinya Kajiura, Ayumu Hosokawa, Naoki Horikawa, Itsuro Terada, Taishi Hata, Yuka Kobayashi, Yuji Tsukioka, Kazuhisa Yabushita, Takashi Matsuo, Hiroki Yoshita, Akira Ueda, Kohei Ogawa, Takayuki Ando, Ryuji Hayashi, Ichiro Yasuda
Abstract Aim 5‐Fluorouracil/folinic acid and oxaliplatin plus bevacizumab (FOLFOX + BV) is a standard chemotherapy regimen for metastatic colorectal cancer (mCRC). This study was aimed at evaluating the preventive effects of shakuyakukanzoto against oxaliplatin‐induced neurotoxicity associated with FOLFOX + BV administration. Methods In this single‐arm, open‐label, phase II clinical trial, we enrolled patients with previously untreated, histologically confirmed mCRC from six hospitals in Japan who were aged 20 years and older and had an Eastern Cooperative Oncology Group performance status of 0–1. The patients received shakuyakukanzoto 2.5 g thrice daily, orally, until disease progression and/or unacceptable toxicity was noted. The primary endpoint was the incidence of neurotoxicity following oxaliplatin administration at a dose of 500 mg/m 2 . Neurotoxicity was evaluated according to the Neurotoxicity Criteria of Debiopharm (DEB‐NTC). The trial was registered in the UMIN Clinical Trials Registry of Japan (UMIN000001853). Results Forty‐one non‐pretreated mCRC patients were included between April 2009 and September 2013. At an oxaliplatin dose of 500 mg/m 2 , neurotoxicity of DEB‐NTC grade 1–2 developed in 25.0% of patients; no patient had DEB‐NTC grade 3 neurotoxicity. The most common grade 3/4 adverse events were neutropenia (34.1%), hypertension (24.4%), and fatigue (9.8%). The response rate of the 38 patients with measurable lesions was 55.2%. The median progression‐free and overall survival was 14.9 and 35.2 months respectively. Conclusion Shakuyakukanzoto substantially reduced oxaliplatin‐induced neurotoxicity without negatively affecting tumor response or survival in FOLFOX + BV‐treated patients with CRC.
目的5‐氟尿嘧啶/亚叶酸+奥沙利铂+贝伐单抗(FOLFOX + BV)是转移性结直肠癌(mCRC)的标准化疗方案。本研究旨在评估shakuyakukanzoto对与FOLFOX + BV给药相关的奥沙利铂诱导的神经毒性的预防作用。方法:在这项单臂、开放标签、II期临床试验中,我们招募了来自日本6家医院的既往未治疗、组织学证实的mCRC患者,这些患者年龄在20岁及以上,东方肿瘤合作组(Eastern Cooperative Oncology Group)评分为0-1。患者接受每日3次,每次2.5 g,口服,直至发现疾病进展和/或不可接受的毒性。主要终点是奥沙利铂剂量为500mg / m2后神经毒性的发生率。根据Debiopharm神经毒性标准(DEB - NTC)评估神经毒性。该试验已在日本UMIN临床试验注册中心注册(UMIN000001853)。结果2009年4月至2013年9月共纳入41例未经预处理的mCRC患者。奥沙利铂剂量为500mg / m2时,25.0%的患者出现DEB - NTC 1-2级的神经毒性;没有患者发生DEB - NTC 3级神经毒性。最常见的3/4级不良事件是中性粒细胞减少(34.1%)、高血压(24.4%)和疲劳(9.8%)。38例可测量病变患者的有效率为55.2%。中位无进展生存期和总生存期分别为14.9个月和35.2个月。结论:在FOLFOX + BV治疗的结直肠癌患者中,Shakuyakukanzoto可显著降低奥沙利铂诱导的神经毒性,而不会对肿瘤反应或生存产生负面影响。
{"title":"Preventive effect of a traditional Japanese Kampo medicine, <i>shakuyakukanzoto</i>, against neurotoxicity of <scp>FOLFOX</scp> plus bevacizumab used for metastatic colorectal cancer management: A single‐arm phase <scp>II</scp> study","authors":"Hiroaki Takagi, Shinya Kajiura, Ayumu Hosokawa, Naoki Horikawa, Itsuro Terada, Taishi Hata, Yuka Kobayashi, Yuji Tsukioka, Kazuhisa Yabushita, Takashi Matsuo, Hiroki Yoshita, Akira Ueda, Kohei Ogawa, Takayuki Ando, Ryuji Hayashi, Ichiro Yasuda","doi":"10.1002/tkm2.1389","DOIUrl":"https://doi.org/10.1002/tkm2.1389","url":null,"abstract":"Abstract Aim 5‐Fluorouracil/folinic acid and oxaliplatin plus bevacizumab (FOLFOX + BV) is a standard chemotherapy regimen for metastatic colorectal cancer (mCRC). This study was aimed at evaluating the preventive effects of shakuyakukanzoto against oxaliplatin‐induced neurotoxicity associated with FOLFOX + BV administration. Methods In this single‐arm, open‐label, phase II clinical trial, we enrolled patients with previously untreated, histologically confirmed mCRC from six hospitals in Japan who were aged 20 years and older and had an Eastern Cooperative Oncology Group performance status of 0–1. The patients received shakuyakukanzoto 2.5 g thrice daily, orally, until disease progression and/or unacceptable toxicity was noted. The primary endpoint was the incidence of neurotoxicity following oxaliplatin administration at a dose of 500 mg/m 2 . Neurotoxicity was evaluated according to the Neurotoxicity Criteria of Debiopharm (DEB‐NTC). The trial was registered in the UMIN Clinical Trials Registry of Japan (UMIN000001853). Results Forty‐one non‐pretreated mCRC patients were included between April 2009 and September 2013. At an oxaliplatin dose of 500 mg/m 2 , neurotoxicity of DEB‐NTC grade 1–2 developed in 25.0% of patients; no patient had DEB‐NTC grade 3 neurotoxicity. The most common grade 3/4 adverse events were neutropenia (34.1%), hypertension (24.4%), and fatigue (9.8%). The response rate of the 38 patients with measurable lesions was 55.2%. The median progression‐free and overall survival was 14.9 and 35.2 months respectively. Conclusion Shakuyakukanzoto substantially reduced oxaliplatin‐induced neurotoxicity without negatively affecting tumor response or survival in FOLFOX + BV‐treated patients with CRC.","PeriodicalId":23213,"journal":{"name":"Traditional & Kampo Medicine","volume":"69 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134885547","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A review of frequently used Kampo prescriptions. Part 3. Yokukansan 常用的汉布方剂述评。第3部分。Yokukansan
Pub Date : 2023-09-26 DOI: 10.1002/tkm2.1386
Hideaki Yamaguchi, Tetsuhiro Yoshino, Hiroaki Oizumi, Ryutaro Arita, Tatsuya Nogami, Shin Takayama
Abstract Background The source of yokukansan (YKS) is thought to be Baoying‐Jinjiang (Hoeikinkyōroku in Japanese) by Xue Ji. YKS was originally designed for children and indicated for spasms, clenching of teeth, digestive dysfunction due to mental instability, and insomnia. Key Findings YKS formula consists of seven types of crude drugs. Clinical studies have revealed that YKS exerts physiological effects including the treatment of behavioral and psychiatric symptoms of dementia (BPSD), preoperative sedation and anxiety, and postoperative delirium. A meta‐analysis showed that YKS could improve BPSD and daily living activities; however, no improvement in cognitive function was observed. Preclinical studies have also reported that YKS modulates neuronal pathways in the central nervous system, including the serotonergic, glutamatergic, GABAergic, and other neurotransmitter pathways. The incidence of adverse events associated with YKS was 5.17%, with the major adverse effect being pseudoaldosteronism. Routine blood sampling is considered for hypokalemia prevention. Conclusion YKS is useful for BPSD and perioperative mental instability. The modulation of the serotonergic and glutamatergic neural pathways is one of mechanisms. Pseudoaldosteronism is one of the side effects.
背景薛骥认为yokukansan (YKS)的来源是宝应晋江(日语:Hoeikinkyōroku)。YKS最初是为儿童设计的,用于痉挛、咬牙、精神不稳定导致的消化功能障碍和失眠。YKS方由7种药材组成。临床研究表明,YKS具有生理作用,包括治疗痴呆(BPSD)的行为和精神症状,术前镇静和焦虑以及术后谵妄。荟萃分析显示,YKS可以改善BPSD和日常生活活动;然而,没有观察到认知功能的改善。临床前研究也报道了YKS调节中枢神经系统的神经通路,包括血清素能、谷氨酸能、gaba能和其他神经递质通路。与YKS相关的不良事件发生率为5.17%,主要不良反应为假性醛固酮增多症。常规采血被认为是预防低钾血症的方法。结论YKS对BPSD及围手术期精神不稳定有较好的治疗效果。5 -羟色胺和谷氨酸神经通路的调节是其机制之一。假性醛固酮增多症是其副作用之一。
{"title":"A review of frequently used Kampo prescriptions. Part 3. Yokukansan","authors":"Hideaki Yamaguchi, Tetsuhiro Yoshino, Hiroaki Oizumi, Ryutaro Arita, Tatsuya Nogami, Shin Takayama","doi":"10.1002/tkm2.1386","DOIUrl":"https://doi.org/10.1002/tkm2.1386","url":null,"abstract":"Abstract Background The source of yokukansan (YKS) is thought to be Baoying‐Jinjiang (Hoeikinkyōroku in Japanese) by Xue Ji. YKS was originally designed for children and indicated for spasms, clenching of teeth, digestive dysfunction due to mental instability, and insomnia. Key Findings YKS formula consists of seven types of crude drugs. Clinical studies have revealed that YKS exerts physiological effects including the treatment of behavioral and psychiatric symptoms of dementia (BPSD), preoperative sedation and anxiety, and postoperative delirium. A meta‐analysis showed that YKS could improve BPSD and daily living activities; however, no improvement in cognitive function was observed. Preclinical studies have also reported that YKS modulates neuronal pathways in the central nervous system, including the serotonergic, glutamatergic, GABAergic, and other neurotransmitter pathways. The incidence of adverse events associated with YKS was 5.17%, with the major adverse effect being pseudoaldosteronism. Routine blood sampling is considered for hypokalemia prevention. Conclusion YKS is useful for BPSD and perioperative mental instability. The modulation of the serotonergic and glutamatergic neural pathways is one of mechanisms. Pseudoaldosteronism is one of the side effects.","PeriodicalId":23213,"journal":{"name":"Traditional & Kampo Medicine","volume":"59 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134886078","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A review of frequently used Kampo prescriptions: Part 2—Hangekobokuto 汉方常用方剂述评:第二部分
Pub Date : 2023-08-01 DOI: 10.1002/tkm2.1373
Tomoko Suzuki, Akiko Kikuchi, Akiyo Kaneko, Ryutaro Arita, T. Nogami, Natsumi Saito, S. Takayama
The origin of hangekobokuto (HKT) is from Jin Gui Yao Lue (Kinkiyōryaku in Japanese), and it has been indicated for treating throat discomfort in women.
hangekobokuto (HKT)的起源是金贵要液(日语Kinkiyōryaku),它被用于治疗女性喉咙不适。
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引用次数: 0
Evaluation of capsules containing Valeriana fauriei root extract for sleep improvement: A randomized, double‐blind, placebo‐controlled, cross‐over comparative trial 缬草根提取物胶囊对睡眠改善的评价:一项随机、双盲、安慰剂对照、交叉比较试验
Pub Date : 2023-07-12 DOI: 10.1002/tkm2.1382
Misato Ota, Yuki Oiwa, Yasuhito Maki, Ichiro Utaka, Sachie Arima, Y. Matsuo, T. Makino, Shunsuke Nojiri
This clinical trial aimed to clarify the sleep‐ameliorating effects of capsules containing Valeriana fauriei root (VF) extract and their adverse effects.
本临床试验旨在阐明缬草根(VF)提取物胶囊的睡眠改善作用及其副作用。
{"title":"Evaluation of capsules containing Valeriana fauriei root extract for sleep improvement: A randomized, double‐blind, placebo‐controlled, cross‐over comparative trial","authors":"Misato Ota, Yuki Oiwa, Yasuhito Maki, Ichiro Utaka, Sachie Arima, Y. Matsuo, T. Makino, Shunsuke Nojiri","doi":"10.1002/tkm2.1382","DOIUrl":"https://doi.org/10.1002/tkm2.1382","url":null,"abstract":"This clinical trial aimed to clarify the sleep‐ameliorating effects of capsules containing Valeriana fauriei root (VF) extract and their adverse effects.","PeriodicalId":23213,"journal":{"name":"Traditional & Kampo Medicine","volume":"4 1","pages":"177 - 184"},"PeriodicalIF":0.0,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76482702","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Overview of diagnostic laboratory tests and diagnostic criteria for liver injury caused by Kampo medicine 康布药引起的肝损伤的诊断实验室检查和诊断标准概述
Pub Date : 2023-07-06 DOI: 10.1002/tkm2.1381
N. Mantani
Several studies have suggested that the known biomarkers and the diagnostic scales are unreliable for the diagnosis of Kampo‐induced liver injury (KMILI).
一些研究表明,已知的生物标志物和诊断量表对于Kampo诱导的肝损伤(KMILI)的诊断不可靠。
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引用次数: 0
Goreisan alleviates cerebral edema: Possibility of its involvement in inhibiting aquaporin‐4 function 葛瑞参减轻脑水肿:其参与抑制水通道蛋白- 4功能的可能性
Pub Date : 2023-06-17 DOI: 10.1002/tkm2.1380
Tomofumi Shimizu, K. Murakami, Chinami Matsumoto, T. Kido, Y. Isohama
In Japan, goreisan (GRS) is used to alleviate cerebral edema and relieve headaches. Although improvement of water maldistribution in the brain may be one of the mechanisms of action of GRS for cerebral edema and headache, scientific evidence is limited. Here, we aimed to investigate the action mechanism of GRS against cerebral edema and headaches, focusing on water dynamics in the brain.
在日本,goreisan (GRS)被用来缓解脑水肿和头痛。虽然改善脑内水分分布不均可能是GRS治疗脑水肿和头痛的作用机制之一,但科学证据有限。本研究旨在探讨GRS对脑水肿和头痛的作用机制,重点关注脑内水动力学。
{"title":"Goreisan alleviates cerebral edema: Possibility of its involvement in inhibiting aquaporin‐4 function","authors":"Tomofumi Shimizu, K. Murakami, Chinami Matsumoto, T. Kido, Y. Isohama","doi":"10.1002/tkm2.1380","DOIUrl":"https://doi.org/10.1002/tkm2.1380","url":null,"abstract":"In Japan, goreisan (GRS) is used to alleviate cerebral edema and relieve headaches. Although improvement of water maldistribution in the brain may be one of the mechanisms of action of GRS for cerebral edema and headache, scientific evidence is limited. Here, we aimed to investigate the action mechanism of GRS against cerebral edema and headaches, focusing on water dynamics in the brain.","PeriodicalId":23213,"journal":{"name":"Traditional & Kampo Medicine","volume":"95 1","pages":"168 - 176"},"PeriodicalIF":0.0,"publicationDate":"2023-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82665081","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Successful treatment of an older patient with COVID‐19 pneumonia using herbal medicine—especially saikanto 使用草药(特别是西关东)成功治疗1例老年COVID - 19肺炎患者
Pub Date : 2023-06-08 DOI: 10.1002/tkm2.1379
T. Utsunomiya, Den-ichiro Yamaoka, T. Asakawa, Yukio Mizumoto, Yasutsugu Takada
New antiviral drugs for COVID-19 have been launched with special approval. However, as there may be a shortage of drugs in the future, it may be difficult to provide appropriate medical intervention. Herein, we describe our experience of successfully treating COVID-19 pneumonia in an older patient using a Japanese herbal medicine without new antiviral drugs. A 94-year-old woman was diagnosed with COVID-19 and received home care. However, dyspnea appeared on day 4 of home treatment, so she visited the emergency department of our hospital. Her SpO2 then increased to 97% after oxygen delivery at a rate of 7 L/min via a mask. On physical examination, the patient presented with tachypnea (24 breaths per minute) and stable hemodynamics. Her blood pressure, heart rate, and body temperature were 104/65 mm Hg, 68 beats/min, and 37.5 C respectively. She had clear consciousness. Her height and body weight were 146 cm and 47 kg respectively. Laboratory test results are presented in Table 1. Computed tomography (CT) scan revealed infiltrates in the bilateral lower lungs with ground-glass signs. The qSOFA was one point and sepsis was not actively suspected, but the A-DROP was three points and the patient was indicated for hospitalization for severe pneumonia. Given her history of hypertension and stroke, she usually spent most of her time lying in bed, except for eating and defecating. Aspiration was not confirmed during home care. CT imaging showed mainly a groundglass appearance rather than an infiltrating shadow, so aspiration pneumonia was not actively suspected. Based on the course and CT imaging, typical bacterial pneumonia was not actively suspected and the use of antibiotics was withheld. Her respiration was stabilized with oxygen therapy; however, she was frail and old, and neither she nor her family wanted active treatment. As she could drink water, a Japanese herbal treatment for pneumonia was initiated. Her Kampo medical findings indicated that she had a deficiency. She complained of bitterness in her mouth and chest pain when coughing. Her pulse was weak
新冠病毒抗病毒药物已获特别批准上市。然而,由于将来可能出现药物短缺,可能难以提供适当的医疗干预。在此,我们描述了我们使用日本草药成功治疗老年患者COVID-19肺炎的经验,没有新的抗病毒药物。一名94岁的妇女被诊断出患有COVID-19并接受了家庭护理。然而,在家庭治疗的第4天出现呼吸困难,因此她来到了我院的急诊科。通过面罩以7l /min的速率给氧后,她的SpO2增加到97%。体格检查时,患者出现呼吸急促(每分钟24次呼吸),血流动力学稳定。她的血压、心率和体温分别为104/65 mm Hg、68次/分和37.5℃。她有清醒的意识。她的身高和体重分别为146厘米和47公斤。实验室测试结果见表1。计算机断层扫描显示双侧下肺浸润伴磨玻璃征。qSOFA为1分,未积极怀疑脓毒症,但A-DROP为3分,患者因严重肺炎需要住院治疗。考虑到她有高血压和中风病史,除了吃饭和排便,她通常大部分时间都躺在床上。在家庭护理期间未确认误吸。CT主要表现为磨砂样影,未见浸润影,不积极怀疑吸入性肺炎。根据病程及CT表现,未积极怀疑为典型细菌性肺炎,未给予抗生素治疗。氧疗稳定了她的呼吸;然而,她年老体弱,她和她的家人都不希望积极治疗。因为她可以喝水,所以开始使用日本草药治疗肺炎。她的康坡医学检查结果表明,她有缺陷。她说嘴里有苦味,咳嗽时胸痛。她的脉搏很微弱
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引用次数: 0
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Traditional & Kampo Medicine
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