{"title":"Study the effect of Dipeptidyl Peptidase 4 Inhibitors as an Antidiabetic in Type 2 Diabetes Mellitus (T2DM)","authors":"A. Yadav, P. Wal, P. Verma","doi":"10.46624/ajptr.2021.v11.i5.009","DOIUrl":null,"url":null,"abstract":"Dipeptidyl peptidase IV is a key regulator of insulin- stimulating hormones, glucagon-like peptide \nand glucose dependent insulinotrophic polypeptide. Thus it is a promising target for treatment of \ntype 2 Diabetes mellitus. Inhibition of plasma Dipeptidyl peptidase IV enzyme lead to enhanced \nendogenous glucagon like peptide-1, GIP activity which ultimately results in the potentiating of \ninsulin secretion by pancreatic cell and subsequent lowering blood glucose level, HbA [1c], \nglucose secretion, liver glucose production. One of the principal goals of diabetes management is \nto attain haemoglobin HbA [1c] treatment goals and prevent the onset or decrease the rate of \noccurrence of Microvascular conditions.2, 6 numerous treatment options are available for \nmanagement of Type 2 Diabetes mellitus, various class of DPP IV inhibitor being explored such as \nSitagliptin and Vildagliptin successfully launched. Several other novel DPP IV inhibitors are in \npipeline, Unless there are clear contraindications, metformin monotherapy is prescribed, and if \nHbA [1c] targets are not attained after 3 months, 1 of several classes of agents could be added, \nsuch as sulfonylurea’s, Thiazolidinediones, dipeptidyl peptidase-4 inhibitors, - glucagon like \npeptide-1 receptor agonists, or basal insulin.2,6 Despite the broad range of therapeutic options, the \nattainment of HbA [1c] goals among patients with diabetes remains challenging, with just slightly \nmore than half (52%) of diabetes patients attaining the common HbA [1c] goal of < 7.0%. The \npresent review summarizes latest preclinical and clinical trial data of different DPP IV inhibitors \nwith a special emphasis on their DPP8/9 fold selectivity and therapeutic advantages over GLP-1 \nbased approach. \nKeywords: Diabetes 2, Dipeptidyl Peptidase-4, glucose-dependent insulinot","PeriodicalId":7701,"journal":{"name":"American Journal of PharmTech Research","volume":"25 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of PharmTech Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46624/ajptr.2021.v11.i5.009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Dipeptidyl peptidase IV is a key regulator of insulin- stimulating hormones, glucagon-like peptide
and glucose dependent insulinotrophic polypeptide. Thus it is a promising target for treatment of
type 2 Diabetes mellitus. Inhibition of plasma Dipeptidyl peptidase IV enzyme lead to enhanced
endogenous glucagon like peptide-1, GIP activity which ultimately results in the potentiating of
insulin secretion by pancreatic cell and subsequent lowering blood glucose level, HbA [1c],
glucose secretion, liver glucose production. One of the principal goals of diabetes management is
to attain haemoglobin HbA [1c] treatment goals and prevent the onset or decrease the rate of
occurrence of Microvascular conditions.2, 6 numerous treatment options are available for
management of Type 2 Diabetes mellitus, various class of DPP IV inhibitor being explored such as
Sitagliptin and Vildagliptin successfully launched. Several other novel DPP IV inhibitors are in
pipeline, Unless there are clear contraindications, metformin monotherapy is prescribed, and if
HbA [1c] targets are not attained after 3 months, 1 of several classes of agents could be added,
such as sulfonylurea’s, Thiazolidinediones, dipeptidyl peptidase-4 inhibitors, - glucagon like
peptide-1 receptor agonists, or basal insulin.2,6 Despite the broad range of therapeutic options, the
attainment of HbA [1c] goals among patients with diabetes remains challenging, with just slightly
more than half (52%) of diabetes patients attaining the common HbA [1c] goal of < 7.0%. The
present review summarizes latest preclinical and clinical trial data of different DPP IV inhibitors
with a special emphasis on their DPP8/9 fold selectivity and therapeutic advantages over GLP-1
based approach.
Keywords: Diabetes 2, Dipeptidyl Peptidase-4, glucose-dependent insulinot