Drosophila as a Rapid Screening Model to Evaluate the Hypoglycemic Effects of Dipeptidyl Peptidase 4 (DPP4) Inhibitors: High Evolutionary Conservation of DPP4

被引:0
|
作者
Lagunas-Rangel, Francisco Alejandro [1 ]
Liao, Sifang [1 ]
Williams, Michael J. [1 ]
Trukhan, Vladimir [2 ]
Fredriksson, Robert [3 ]
Schioth, Helgi B. [1 ]
机构
[1] Uppsala Univ, Dept Surg Sci Funct Pharmacol & Neurosci, S-75124 Uppsala, Sweden
[2] Adv Mol Technol LLC, Moscow 354340, Russia
[3] Uppsala Univ, Dept Pharmaceut Biosci, Uppsala, Sweden
基金
瑞典研究理事会;
关键词
diabetes; alternative animal model; new drugs; glucose levels; DRUG DISCOVERY; RECEPTOR; SYSTEM; SAFETY;
D O I
10.3390/biomedicines11113032
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dipeptidyl peptidase 4 (DPP4) inhibitors, commonly known as gliptins, have been an integral part of the treatment of type 2 diabetes mellitus (T2DM) for several years. Despite their remarkable efficacy in lowering glucose levels and their compatibility with other hypoglycemic drugs, recent studies have revealed adverse effects, prompting the search for improved drugs within this category, which has required the use of animal models to verify the hypoglycemic effects of these compounds. Currently, in many countries the use of mammals is being significantly restricted, as well as cost prohibitive, and alternative in vivo approaches have been encouraged. In this sense, Drosophila has emerged as a promising alternative for several compelling reasons: it is cost-effective, offers high experimental throughput, is genetically manipulable, and allows the assessment of multigenerational effects, among other advantages. In this study, we present evidence that diprotin A, a DPP4 inhibitor, effectively reduces glucose levels in Drosophila hemolymph. This discovery underscores the potential of Drosophila as an initial screening tool for novel compounds directed against DPP4 enzymatic activity.
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页数:14
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