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Solid phase synthesis of fatty acid modified glucagon-like peptide-1(7-36) amide under thermal and controlled microwave irradiation
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作者 Ni, Shuai Han Zhang, Hui Bin +2 位作者 Huang, Wen Long Zhou, Jin Pei Qian, Hai 《Chinese Chemical Letters》 SCIE CAS CSCD 2010年第1期27-30,共4页
Fatty acid modified glucagon-like peptide-1(7-36) amide was synthesized efficiently on Rink-Amide-MBHA resin by microwave-assisted solid phase method.The method of thermal and controlled microwave irradiation provided... Fatty acid modified glucagon-like peptide-1(7-36) amide was synthesized efficiently on Rink-Amide-MBHA resin by microwave-assisted solid phase method.The method of thermal and controlled microwave irradiation provided impressive enhancements in product yield,selectivity,and reaction rate.The coupling time was dramatically decreased to 6 min,and the desired products were obtained in high yield and purity. 展开更多
关键词 glucagon-like peptide-1 glp-1 MICROWAVE Solid phase Fatty acid modification
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Electroacupuncture for functional dyspepsia and the influence on serum Ghrelin, CGRP and GLP-1 levels 被引量:9
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作者 Liming QIANG Yuan ]IANG 《World Journal of Acupuncture-Moxibustion》 CSCD 2018年第2期16-20,80,81,共7页
Objective: To observe the clinical efficacy of electroacupuncture for functional dyspepsia(FD), and explore the corresponding mechanism.Methods: Sixty-four FD patients were randomly divided into electroacupuncture... Objective: To observe the clinical efficacy of electroacupuncture for functional dyspepsia(FD), and explore the corresponding mechanism.Methods: Sixty-four FD patients were randomly divided into electroacupuncture group and western medicine group, with 32 cases in each group. In electroacupuncture group, electroacupuncture at Zusanli(足三里ST 36),Sanyinjiao(三阴交SP 6),Gongsun(公孙SP 4) and Neiguan(内关PC 6) was performed for once a day, and the needles were retained for 30 min. In western medicine group, oral administration of mosapride citrate dispersible tablets in a dosage of 5 mg/time was carried out for 3 times a day. Treatment was conducted for 30 consecutive days in both groups. The scores of Leeds dyspepsia questionnaire(LDQ) and functional digestive disorder quality of life(FDDQL) of patients in both groups were recorded before and after treatment. Serum Ghrelin, CGRP and GLP-1 levels of patients were tested before and after treatment respectively, and the clinical efficacy of patients in both groups was evaluated after treatment.Results: In western medicine group, LDQ score after treatment was lower than that before treatment(P 0.05), FDDQL score after treatment was higher than that before treatment, while the differences were not statistically significant(P0.05). LDQ score in electroacupuncture group after treatment was lower than that before treatment(P0.05), and also lower than that in western medicine group at the same time point(P 0.05). FDDQL score in electroacupuncture group after treatment was higher than that before treatment(P0.05), and also higher than that in western medicine group at the same time point(P0.05). In western medicine group, Ghrelin level after treatment was higher than that before treatment(P 0.05), CGRP level reduced, and the differences were not statistically significant(P 0.05). GLP-1 level after treatment was also higher than that before treatment(P0.05). In electroacupuncture group,Ghrelin level after treatment was higher than that before treatment, CGRP level reduced, and GLP-1 level after treatment was also higher than that before treatment(both P 0.05). According to the comparison of values of each index between electroacupuncture group and western medicine group after treatment,the differences were all statistically significant(all P 0.05). The total effective rate in electroacupuncture group was 90.63%(29/32) which was higher than that in western medicine group 68.75%(22/32), and the differences were statistically significant(P0.05).Conclusion: Electroacupuncture at ST 36, SP 6, SP 4 and PC 6 can effectively improve the clinical symptoms of FD patients, and the mechanism might be related with the increase of serum Ghrelin and GLP-1 levels and the decrease of serum CGRP level. 展开更多
关键词 Functional dyspepsia Electroacupuncture Ghrelin Calcitonin gene-related peptide (CGRP) glucagon-like peptide-1 (glp-1)
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Exenatide reduces doxorubicin-induced cardiac injury
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作者 Juntao Fang Lijuan Wang +4 位作者 Xiaoman Zhang Shangyu Liu Hui Liu Tiewei Li Ping Li 《中国循环杂志》 CSCD 北大核心 2018年第S01期130-131,共2页
Objective Doxorubicin(Dox)is an effective antitumor drug,which is limited due to its lethal cardiac injury in clinical application.Exenatide(Exe)is a glucagon-like peptide-1(GLP-1)analog,it can not only regulate blood... Objective Doxorubicin(Dox)is an effective antitumor drug,which is limited due to its lethal cardiac injury in clinical application.Exenatide(Exe)is a glucagon-like peptide-1(GLP-1)analog,it can not only regulate blood glucose,but protect the myocardium by reducing inflammation,oxidative stress and cell apoptosis.Since doxorubicininduced cardiac injury is currently thought to be mainly caused by inflammation,oxidative stress and cell apoptosis,we hypothesized that prophylactic treatment with exenatide may alleviate doxorubicin-induced cardiac injury. 展开更多
关键词 DOXORUBICIN EXENATIDE glucagon-like peptide-1(glp-1)
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GLP-1R Agonists Therapy for Type 2 Diabetes
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作者 ZHOU Bilan PENG Anlin +1 位作者 GONG Hao HUANG Kun 《Wuhan University Journal of Natural Sciences》 CAS 2014年第1期27-33,共7页
Glucagon-like peptide-1 receptor (GLP-1R) agonists are widely used for treating type 2 diabetes mellitus (T2DM) be- cause of their glucose-lowering and weight-losing effects, and low risk of hypoglycemia. Hence, t... Glucagon-like peptide-1 receptor (GLP-1R) agonists are widely used for treating type 2 diabetes mellitus (T2DM) be- cause of their glucose-lowering and weight-losing effects, and low risk of hypoglycemia. Hence, there is considerable interest in understanding the mechanism underlying the beneficial effects of GLP-I and developing stable and effective GLP-1R agonists. Here, we summarize the presently known mechanism of GLP-I actions, which are mainly through regulating cAMP-PKA signaling pathway; the latest developments in novel clinical GLP-1R agonists are also introduced, which are characterized with multiple properties, such as extended half-life, reduced side-effects, lower production costs and more convenient drug dosing mode. The potential risk of GLP-I-based therapeutics, an often-ignored fact, is also discussed. 展开更多
关键词 glucagon-like peptide-I receptor (glp-1R) glp- 1R agonists type 2 diabetes
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Advances in reducing cardiovascular risk in the management of patients with type 2 diabetes mellitus
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作者 Ying Hu 《Chronic Diseases and Translational Medicine》 CSCD 2019年第1期25-36,共12页
Treatment intended to lower cardiovascular (CV) risk in patients with diabetes has always been a primary goal of diabetes treatment. Due to the subdued effects of reducing hemoglobin A1c (HbA1c) on macrovascular compl... Treatment intended to lower cardiovascular (CV) risk in patients with diabetes has always been a primary goal of diabetes treatment. Due to the subdued effects of reducing hemoglobin A1c (HbA1c) on macrovascular complications, controlling other CV risk factors such as hypertension and hyperlipidemia instead of hyperglycemia has been the mainstay treatment to improve CV outcome in patients with type 2 diabetes mellitus (T2DM) until recent years. This review is intended to summarize and compare the results from the available cardiovascular outcome trials (CVOTs) for the two classes of glucose lowering drug: sodium-glucose cotransporter 2 inhibitor (SGLT2i) and glucagon-like peptide-1 receptor agonist (GLP-1 RA). The results including the EMPA-REG, CANVAS program and DECLARE-TIMI 58 trials for SGLT2i, and the ELIXA, LEADER, SUSTAIN-6, EXSCEL and HARMONY trials for GLP-1 RA were summarized. The potential mechanisms of these CV beneficial effects and the optimal CV risk reduction treatment in patients with T2DM based on patient risk stratification and evidence from these CVOTs in real-world setting were discussed. 展开更多
关键词 Type 2 diabetes MELLITUS (T2DM) CARDIOVASCULAR risk CARDIOVASCULAR outcome trial (CVOT) Sodium-glucose co-transporter 2 inhibitor (SGLT2i) glucagon-like peptide-1 receptor AGONIST (glp-1 RA)
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