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      Antidiabetic and Antiobesity Effects of Artemether in db/db Mice

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          Abstract

          This study is designed to investigate the effect of artemether on type 2 diabetic db/db mice. The experiments consisted of three groups: normal control (NC, db/+, 1% methylcellulose, intragastric administration), diabetic control (DM, db/db, 1% methylcellulose, intragastric administration), and artemether treated (artemether, db/db, 200 mg/kg of artemether, intragastric administration). The treatment lasted for two weeks. The food intake, body weight, and fasting blood glucose of mice were measured every three days. At the start and end of the experiment, the intraperitoneal glucose tolerance test (IPGTT) and insulin tolerance test (IPITT) were performed. We determined the serum insulin and glucagon levels by ELISA kits and calculated insulin resistance index (HOME-IR). HE staining was used to observe the morphologies of pancreas and liver in mice. The damage of pancreatic beta cells was evaluated by TUNEL staining and immunofluorescence. We found the following: (1) compared with the DM group, the food intake and weight increase rate of artemether group significantly reduced ( P < 0.05); (2) compared with pretreatment, artemether significantly reduced the fasting blood glucose levels, and the areas under the curves (AUCs) of IPGTT were decreased significantly, increasing the tolerance to glucose of db/db mice. ( P < 0.05); (3) artemether improved hyperinsulinemia and decreased the AUCs of IPITT and HOME-IR, increasing the insulin sensitivity of db/db mice. (4) Artemether significantly ameliorated islet vacuolar degeneration and hepatic steatosis in db/db mice. (5) Artemether reduced the apoptosis of pancreatic beta cells and increased insulin secretion in db/db mice compared with DM group ( P < 0.05). Our results indicated that artemether significantly improved glucose homeostasis and insulin resistance and had the potential activity to prevent obesity, reduced the severity of fatty liver, and protected pancreatic beta cells, promising to treat type 2 diabetes.

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          Artemisinin-A Gift from Traditional Chinese Medicine to the World (Nobel Lecture).

          Youyou Tu (2016)
          Malaria has long been a devastating and life-threatening global epidemic disease in human history. Artemisinin, the active substance against malaria, was first isolated and tested in the 1970s in China. The important role played by traditional Chinese medicine in the discovery of artemisinin is described by Y. Tu in her Nobel Lecture.
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            The antiviral activities of artemisinin and artesunate.

            Traditional Chinese medicine commands a unique position among all traditional medicines because of its 5000 years of history. Our own interest in natural products from traditional Chinese medicine was triggered in the 1990s, by artemisinin-type sesquiterpene lactones from Artemisia annua L. As demonstrated in recent years, this class of compounds has activity against malaria, cancer cells, and schistosomiasis. Interestingly, the bioactivity of artemisinin and its semisynthetic derivative artesunate is even broader and includes the inhibition of certain viruses, such as human cytomegalovirus and other members of the Herpesviridae family (e.g., herpes simplex virus type 1 and Epstein-Barr virus), hepatitis B virus, hepatitis C virus, and bovine viral diarrhea virus. Analysis of the complete profile of the pharmacological activities and molecular modes of action of artemisinin and artesunate and their performance in clinical trials will further elucidate the full antimicrobial potential of these versatile pharmacological tools from nature.
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              Clinical significance, pathogenesis, and management of postprandial hyperglycemia.

              It is well established that strict glycemic control (hemoglobin A1c 140 mg/dL [>7.8 mmol/L]) in the face of normal fasting plasma glucose (<110 mg/dL [<6.1 mmol/L]) and normal hemoglobin A1c (<6.1%) values is associated with a 2-fold increased risk of death from cardiovascular disease. These observations imply that more strict glycemic control is required to prevent macrovascular disease than microvascular disease. This review summarizes epidemiologic and experimental studies linking postprandial hyperglycemia to cardiovascular disease and therapeutic approaches available and in development to treat this disorder.
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                Author and article information

                Contributors
                Journal
                Biomed Res Int
                Biomed Res Int
                BMRI
                BioMed Research International
                Hindawi
                2314-6133
                2314-6141
                2018
                13 May 2018
                : 2018
                : 8639523
                Affiliations
                1Department of Endocrinology, The First Affiliated Hospital and College of Clinical Medicine of Henan University of Science and Technology, Luoyang 471003, China
                2Key Laboratory of Endocrinology Inherited and Metabolic Diseases of Luoyang, Luoyang 471003, China
                3Clinical Medicine Research Center of Endocrine and Metabolic Disease of Luoyang, Luoyang 471003, China
                4Academican Workstation for Diabetic Kidney Disease Research of Henan Province, Luoyang 471003, China
                Author notes

                Academic Editor: Goutam Ghosh Choudhury

                Author information
                http://orcid.org/0000-0002-8091-6734
                http://orcid.org/0000-0002-4611-8819
                http://orcid.org/0000-0002-6050-4257
                http://orcid.org/0000-0001-8404-0664
                http://orcid.org/0000-0003-2738-2080
                http://orcid.org/0000-0001-8471-8164
                http://orcid.org/0000-0001-8083-7596
                http://orcid.org/0000-0001-7396-1310
                http://orcid.org/0000-0003-2054-3398
                http://orcid.org/0000-0003-3807-7989
                Article
                10.1155/2018/8639523
                5971258
                29862294
                a2c60573-0b3c-4dd5-b1e0-3228d7ea8228
                Copyright © 2018 Yu Guo et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 13 December 2017
                : 18 March 2018
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: U1404805
                Funded by: Henan University of Science and Technology
                Award ID: CXJJ-2016-ZR15
                Categories
                Research Article

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