Ontology highlight
ABSTRACT: Unlabelled
Apolipoprotein C1 (ApoC1) is a component of multiple lipoproteins where it performs a variety of roles in lipid metabolism and transport. ApoC1 exists as both full-length and truncated isoforms. Truncation of ApoC1 has been postulated to result from the action of dipeptidyl peptidase-4 (DPP-4), the target of a new class of diabetes drugs that includes sitagliptin phosphate. In this study, we sought to determine if oral administration of sitagliptin altered the proportion of ApoC1 isoforms circulating in humans. Results indicated a dramatic change in ApoC1 truncation, consistent with a high level of DPP-4 inhibition by sitagliptin.Funding
University of Minnesota, Minneapolis, MN, USA.
SUBMITTER: Skinner NE
PROVIDER: S-EPMC4575309 | biostudies-literature | 2015 Sep
REPOSITORIES: biostudies-literature
Skinner Nicole E B NE Wroblewski Matthew S MS Kirihara Julie A JA Nelsestuen Gary L GL Seaquist Elizabeth R ER
Diabetes therapy : research, treatment and education of diabetes and related disorders 20150722 3
<h4>Unlabelled</h4>Apolipoprotein C1 (ApoC1) is a component of multiple lipoproteins where it performs a variety of roles in lipid metabolism and transport. ApoC1 exists as both full-length and truncated isoforms. Truncation of ApoC1 has been postulated to result from the action of dipeptidyl peptidase-4 (DPP-4), the target of a new class of diabetes drugs that includes sitagliptin phosphate. In this study, we sought to determine if oral administration of sitagliptin altered the proportion of Ap ...[more]