Literature DB >> 25054271

Novel approaches to drug discovery for the treatment of type 2 diabetes.

Xing Xu1, Gaihong Wang, Tingting Zhou, Lili Chen, Jing Chen, Xu Shen.   

Abstract

INTRODUCTION: Type 2 diabetes mellitus (T2DM) is a chronic, complex and multifactorial metabolic disorder, which has become a serious global health problem. The side effects of known drugs and the deficiency of long-term safety data, in addition to the already determined adverse effects for the current preclinical drugs against T2DM, have largely called upon the urgent exploration of novel therapeutic and preventative strategies against this disease. AREAS COVERED: The authors highlight the potential approaches for anti-T2DM drug discovery by focusing on: the restoration of pancreatic β-cell mass, the promotion of insulin secretion, the regulation of oxidative stress and endoplasmic reticulum (ER) stress and the modulation of autophagy. EXPERT OPINION: T2DM is based on the gradual development of insulin resistance and β-cell dysfunction. Thus, the restoration of β-cell function is considered as one of the promising therapeutic strategies against T2DM. The stress factors, such as oxidative stress, ER stress and autophagy, play potent roles in the regulation of β-cell apoptosis, insulin secretion and sensitivity in the development of T2DM involving complicated cross-talks. Based on multiplex stress-involved regulatory networks, more and more novel potential targets have been discovered and the multi-targeted drug leads are expected to help develop more effective clinical agents for the treatment of T2DM.

Entities:  

Keywords:  autophagy; endoplasmic reticulum stress; insulin secretion; oxidative stress; type 2 diabetes; β-cell mass

Mesh:

Substances:

Year:  2014        PMID: 25054271     DOI: 10.1517/17460441.2014.941352

Source DB:  PubMed          Journal:  Expert Opin Drug Discov        ISSN: 1746-0441            Impact factor:   6.098


  7 in total

Review 1.  Alternative Medicine in Diabetes - Role of Angiogenesis, Oxidative Stress, and Chronic Inflammation.

Authors:  Mohamed F El-Refaei; Suha H Abduljawad; Ahmed H Alghamdi
Journal:  Rev Diabet Stud       Date:  2015-02-10

2.  HWL-088, a new potent free fatty acid receptor 1 (FFAR1) agonist, improves glucolipid metabolism and acts additively with metformin in ob/ob diabetic mice.

Authors:  Yueming Chen; Qiang Ren; Zongtao Zhou; Liming Deng; Lijun Hu; Luyong Zhang; Zheng Li
Journal:  Br J Pharmacol       Date:  2020-02-08       Impact factor: 8.739

3.  Antidiabetic Effects of the Ethanolic Root Extract of Uvaria chamae P. Beauv (Annonaceae) in Alloxan-Induced Diabetic Rats: A Potential Alternative Treatment for Diabetes Mellitus.

Authors:  Jonathan Emeka Emordi; Esther Oluwatoyin Agbaje; Ibrahim Adekunle Oreagba; Osede Ignis Iribhogbe
Journal:  Adv Pharmacol Sci       Date:  2018-11-08

4.  Synthesis, Structural Studies, and α-Glucosidase Inhibitory, Antidiabetic, and Antioxidant Activities of 2,3-Dihydroquinazolin-4(1H)-ones Derived from Pyrazol-4-carbaldehyde and Anilines.

Authors:  Alireza Barmak; Khodabakhsh Niknam; Gholamhossein Mohebbi
Journal:  ACS Omega       Date:  2019-10-25

Review 5.  Modeling and simulation in medical sciences: an overview of specific applications based on research experience in EMRI (Endocrinology and Metabolism Research Institute of Tehran University of Medical Sciences).

Authors:  Azadeh Ebrahim-Habibi; Elaheh Kashani-Amin; Bagher Larijani
Journal:  J Diabetes Metab Disord       Date:  2021-01-22

6.  Novel fatty chain-modified GLP-1R G-protein biased agonist exerts prolonged anti-diabetic effects through targeting receptor binding sites.

Authors:  Maorong Wang; Ping Yao; Minpeng Gao; Jian Jin; Yerong Yu
Journal:  RSC Adv       Date:  2020-02-24       Impact factor: 4.036

7.  SP6616 as a new Kv2.1 channel inhibitor efficiently promotes β-cell survival involving both PKC/Erk1/2 and CaM/PI3K/Akt signaling pathways.

Authors:  T T Zhou; L L Quan; L P Chen; T Du; K X Sun; J C Zhang; L Yu; Y Li; P Wan; L L Chen; B H Jiang; L H Hu; J Chen; X Shen
Journal:  Cell Death Dis       Date:  2016-05-05       Impact factor: 8.469

  7 in total

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