Skip to main content
Top
Published in: Diabetologia 7/2005

01-07-2005 | Short communication

Dose–response for glycaemic and metabolic changes 28 days after single injection of long-acting release exenatide in diabetic fatty Zucker rats

Authors: B. R. Gedulin, P. Smith, K. S. Prickett, M. Tryon, S. Barnhill, J. Reynolds, L. L. Nielsen, D. G. Parkes, A. A. Young

Published in: Diabetologia | Issue 7/2005

Login to get access

Abstract

Aims/hypothesis

Exenatide (exendin-4) injected subcutaneously twice daily reduces glycaemic deterioration in diabetic fatty Zucker (ZDF) rats and reduces HbA1c in humans with type 2 diabetes. Because tachyphylaxis may develop with continuous peptide exposure, we examined the activity of a long-acting-release (LAR) formulation of exenatide on HbA1c, insulin sensitivity and beta cell secretion in ZDF rats.

Methods

Single subcutaneous injections of a poly-lactide-glycolide microsphere suspension (3% peptide) containing 0, 1, 10, 100, 1,000, 3,000 or 9,000 μg exenatide were administered to 9-week-old ZDF rats with matched initial HbA1c values (n=7 rats/group).

Results

In contrast to the progressive 3.22±0.42% increase in HbA1c in control ZDF rats observed over 28 days, single exenatide-LAR injections dose-proportionally prevented such glycaemic deterioration (median effective dose 74 μg±0.1 log per rat; median effective concentration 52 pmol/l±0.06 log). Hyperinsulinaemic–euglycaemic clamp procedures incorporating an intraclamp glucose challenge performed 28 days after treatment revealed increases in beta cell response to the glucose challenge at lower exenatide-LAR doses, and up to a 2.1-fold increase in insulin sensitivity at higher exenatide-LAR doses.

Conclusions/interpretation

The finding that a single dose of exenatide-LAR enhanced glucose control for 28 days in the ZDF rat model of type 2 diabetes suggests that tachyphylaxis is unlikely to be a feature of exenatide-LAR preparations, and supports further clinical exploration.
Literature
1.
go back to reference Eng J, Kleinman WA, Singh L, Singh G, Raufman JP (1992) Isolation and characterization of exendin-4, an exendin-3 analogue, from Heloderma suspectum venom. Further evidence for an exendin receptor on dispersed acini from guinea pig pancreas. J Biol Chem 267:7402–7405PubMed Eng J, Kleinman WA, Singh L, Singh G, Raufman JP (1992) Isolation and characterization of exendin-4, an exendin-3 analogue, from Heloderma suspectum venom. Further evidence for an exendin receptor on dispersed acini from guinea pig pancreas. J Biol Chem 267:7402–7405PubMed
2.
go back to reference Chen YQE, Drucker DJ (1997) Tissue-specific expression of unique mRNAs that encode proglucagon-derived peptides or exendin 4 in the lizard. J Biol Chem 272:4108–4115PubMed Chen YQE, Drucker DJ (1997) Tissue-specific expression of unique mRNAs that encode proglucagon-derived peptides or exendin 4 in the lizard. J Biol Chem 272:4108–4115PubMed
3.
go back to reference Goke R, Fehmann HC, Linn T et al (1993) Exendin-4 is a high potency agonist and truncated exendin-(9-39)-amide an antagonist at the glucagon-like peptide 1-(7-36)-amide receptor of insulin-secreting beta-cells. J Biol Chem 268:19650–19655PubMed Goke R, Fehmann HC, Linn T et al (1993) Exendin-4 is a high potency agonist and truncated exendin-(9-39)-amide an antagonist at the glucagon-like peptide 1-(7-36)-amide receptor of insulin-secreting beta-cells. J Biol Chem 268:19650–19655PubMed
4.
go back to reference Nielsen LL, Young AA, Parkes DG (2004) Pharmacology of exenatide (synthetic exendin-4): a potential therapeutic for improved glycemic control of type 2 diabetes. Regul Pept 117:77–88PubMed Nielsen LL, Young AA, Parkes DG (2004) Pharmacology of exenatide (synthetic exendin-4): a potential therapeutic for improved glycemic control of type 2 diabetes. Regul Pept 117:77–88PubMed
5.
go back to reference Xu G, Stoffers DA, Habener JF, Bonner-Weir S (1999) Exendin-4 stimulates both beta-cell replication and neogenesis, resulting in increased beta-cell mass and improved glucose tolerance in diabetic rats. Diabetes 48:2270–2276PubMed Xu G, Stoffers DA, Habener JF, Bonner-Weir S (1999) Exendin-4 stimulates both beta-cell replication and neogenesis, resulting in increased beta-cell mass and improved glucose tolerance in diabetic rats. Diabetes 48:2270–2276PubMed
6.
go back to reference Fehse FC, Trautmann ME, Holst JJ et al (2004) Effects of exenatide on first and second phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes. Diabetes 53[Suppl 2]:A82. Abstract 351-OR Fehse FC, Trautmann ME, Holst JJ et al (2004) Effects of exenatide on first and second phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes. Diabetes 53[Suppl 2]:A82. Abstract 351-OR
7.
go back to reference Buse JB, Henry RR, Han J, Kim DD, Fineman MS, Baron AD (2004) Effects of exenatide (exendin-4) on glycemic control over 30 weeks in sulfonylurea-treated patients with type 2 diabetes. Diabetes Care 27:2628–2635PubMed Buse JB, Henry RR, Han J, Kim DD, Fineman MS, Baron AD (2004) Effects of exenatide (exendin-4) on glycemic control over 30 weeks in sulfonylurea-treated patients with type 2 diabetes. Diabetes Care 27:2628–2635PubMed
8.
go back to reference Petrella E, Waterhouse T, Estrada-Stolpe DHR (2001) Development and validation of an immunoenzymetric assay (IEMA) for the quantitation of AC2993 (exendin-4) in plasma and its application to preclinical toxicity evaluations. AAPS PharmSci 3(3) Petrella E, Waterhouse T, Estrada-Stolpe DHR (2001) Development and validation of an immunoenzymetric assay (IEMA) for the quantitation of AC2993 (exendin-4) in plasma and its application to preclinical toxicity evaluations. AAPS PharmSci 3(3)
9.
go back to reference Young AA, Gedulin BR, Bhavsar S et al (1999) Glucose-lowering and insulin-sensitising actions of exendin-4: studies in obese diabetic (ob/ob, db/db) mice, diabetic Fatty Zucker rats and diabetic rhesus monkeys (Macaca mulatta). Diabetes 48:1026–1034PubMed Young AA, Gedulin BR, Bhavsar S et al (1999) Glucose-lowering and insulin-sensitising actions of exendin-4: studies in obese diabetic (ob/ob, db/db) mice, diabetic Fatty Zucker rats and diabetic rhesus monkeys (Macaca mulatta). Diabetes 48:1026–1034PubMed
10.
go back to reference Degn KB, Brock B, Juhl CB et al (2004) Effect of intravenous infusion of exenatide (synthetic exendin-4) on glucose-dependent insulin secretion and counterregulation during hypoglycemia. Diabetes 53:2397–2403PubMed Degn KB, Brock B, Juhl CB et al (2004) Effect of intravenous infusion of exenatide (synthetic exendin-4) on glucose-dependent insulin secretion and counterregulation during hypoglycemia. Diabetes 53:2397–2403PubMed
11.
go back to reference Gedulin BR, Nikoulina SE, Smith PA et al (2005) Exenatide (exendin-4) improves insulin sensitivity and β-cell mass in insulin-resistant obese fa/fa Zucker rats independent of glycemia and body weight. Endocrinology 146:2069–2076PubMed Gedulin BR, Nikoulina SE, Smith PA et al (2005) Exenatide (exendin-4) improves insulin sensitivity and β-cell mass in insulin-resistant obese fa/fa Zucker rats independent of glycemia and body weight. Endocrinology 146:2069–2076PubMed
12.
go back to reference Zhou J, Pineyro MA, Wang X, Doyle ME, Egan JM (2002) Exendin-4 differentiation of a human pancreatic duct cell line into endocrine cells: involvement of PDX-1 and HNF3beta transcription factors. J Cell Physiol 192:304–314PubMed Zhou J, Pineyro MA, Wang X, Doyle ME, Egan JM (2002) Exendin-4 differentiation of a human pancreatic duct cell line into endocrine cells: involvement of PDX-1 and HNF3beta transcription factors. J Cell Physiol 192:304–314PubMed
13.
go back to reference Zhou J, Wang X, Pineyro MA, Egan JM (1999) Glucagon-like peptide 1 and exendin-4 convert pancreatic AR42J cells into glucagon- and insulin-producing cells. Diabetes 48:2358–2366PubMed Zhou J, Wang X, Pineyro MA, Egan JM (1999) Glucagon-like peptide 1 and exendin-4 convert pancreatic AR42J cells into glucagon- and insulin-producing cells. Diabetes 48:2358–2366PubMed
14.
go back to reference Hiles R, Carpenter T, Serota D et al (2004) Exenatide does not cause pancreatic islet cell proliferative lesions in rats and mice following 2-year exposure. Diabetes 53[Suppl 2]:A380 (Abstract) Hiles R, Carpenter T, Serota D et al (2004) Exenatide does not cause pancreatic islet cell proliferative lesions in rats and mice following 2-year exposure. Diabetes 53[Suppl 2]:A380 (Abstract)
15.
go back to reference Pittner RA, Moore CX, Bhavsar SP et al (2004) Effects of PYY[3-36] in rodent models of diabetes and obesity. Int J Obes Relat Metab Disord 28:963–971PubMed Pittner RA, Moore CX, Bhavsar SP et al (2004) Effects of PYY[3-36] in rodent models of diabetes and obesity. Int J Obes Relat Metab Disord 28:963–971PubMed
Metadata
Title
Dose–response for glycaemic and metabolic changes 28 days after single injection of long-acting release exenatide in diabetic fatty Zucker rats
Authors
B. R. Gedulin
P. Smith
K. S. Prickett
M. Tryon
S. Barnhill
J. Reynolds
L. L. Nielsen
D. G. Parkes
A. A. Young
Publication date
01-07-2005
Publisher
Springer-Verlag
Published in
Diabetologia / Issue 7/2005
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-005-1795-2

Other articles of this Issue 7/2005

Diabetologia 7/2005 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine