Biological activity of EXf, a peptide analogue of exendin-4.
Eur J Pharmacol · 2010
Last updated 2026-05-28In lab tests on mice, a shortened version of the diabetes drug exendin-4 called EXf lowered blood sugar levels and reduced spikes after sugar intake in both healthy and diabetic mice. EXf also increased early insulin release in response to sugar and slowed digestion in the mice. The effects were blocked by a GLP-1 receptor blocker, suggesting EXf works by activating the same pathway as GLP-1 drugs.
AI summary of the abstract below.
| Journal | Eur J Pharmacol, 2010 |
|---|---|
| Citations | 7 |
| Relative citation ratio | 0.18 |
| NIH percentile | 12 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Obesity |
Abstract
Exendin-4 is an incretin mimetic that has been developed for the treatment of patients with type 2 diabetes. EXf is an available carboxy-terminal truncated fragment of exendin-4 with two amino acid substitutions. The purpose of these studies was to evaluate the biological activity of EXf. After a single subcutaneous injection, EXf significantly decreased plasma glucose concentration and glucose excursion following the administration of an oral glucose challenge both in non-diabetic (ICR), monosodium l-glutamate induced insulin resistance (MSG-IR) and diabetic KK-ay mice. Meanwhile, EXf resulted in an increase of first-phase insulin secretion in normal mice and KK-ay mice following the glucose challenge. EXf was also shown to inhibit small intestinal transit in rodent models. EXf activated the cAMP response element (CRE) of the rat insulin I gene promoter (RIP1) GFP-construct in a dose-dependent manner in the cultured mouse insulinoma cell line, termed NIT-1, and this agonist activity was blocked by the glucagon-like peptide 1 (GLP-1) receptor antagonist exendin(9-39). In summary, EXf, an analogue of exendin-4, has agonist activity to GLP-1 receptor in vitro and glucoregulatory activities in vivo, thus it can be considered as a new candidate for the treatment of type 2 diabetes.
Verbatim abstract via PubMed 19919832 ↗