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Improvement of glucose tolerance in Zucker diabetic fatty rats by long-term treatment with the dipeptidyl peptidase inhibitor P32/98: comparison with and combination with rosiglitazone.
Diabetes Obes Metab. 2005 Mar; 7(2):170-81.DO

Abstract

AIM

The aim of this study was to investigate the effect of long-term treatment with the dipeptidyl peptidase inhibitor P32/98 and its combination with rosiglitazone on blood glucose control and islet of Langerhans histology in male Zucker diabetic fatty (ZDF) rats, when treatment begins before or after the development of overt diabetes.

METHODS

ZDF rats were treated with P32/98 from the age of 9, 12 or 15 weeks. Rosiglitazone maleate was given to a separate group from the age of 13 weeks. P32/98 was given to all of these rosiglitazone-treated rats from 16 weeks of age. Rosiglitazone maleate was also given from 16 weeks of age to half the rats that were given P32/98 from 9 weeks of age. The compounds were given by oral gavage until the rats were 14 weeks old and then in the diet. The experiment was terminated at the age of 20-21 weeks. Blood glucose, plasma insulin and oral glucose tolerance were measured at intervals; islet histology was assessed terminally.

RESULTS

P32/98 improved glucose tolerance after both single and multiple doses when treatment started at 9 weeks of age, also after the third week of treatment when treatment began at 12 or 15 weeks of age. P32/98 reduced daytime blood glucose when treatment began at 12 weeks. Treatment with rosiglitazone increased food intake and body weight, and after 2 weeks, reduced daytime blood glucose, water intake and the area under the glucose tolerance curve. A single dose of P32/98 markedly improved glucose tolerance in rosiglitazone-treated rats. When treatment had begun at 9 weeks of age, P32/98 stimulated insulin secretion in some glucose tolerance tests. Neither P32/98 nor rosiglitazone affected pancreatic insulin content, nor did they have clear effects on islet histology.

CONCLUSION

P32/98 elicited a sustained improvement in glucose tolerance in both prediabetic and diabetic ZDF rats. The effects of P32/98 on glucose and insulin were similar to those of rosiglitazone, and in contrast to rosiglitazone, P32/98 did not increase food intake or body weight. However, neither compound was especially effective at improving diabetes in ZDF rats when treatment began at 9, 12 or 15 (P32/98) or 13 (rosiglitazone) weeks of age.

Authors+Show Affiliations

Clore Laboratory, University of Buckingham, Buckingham, UK.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

15715890

Citation

Wargent, E, et al. "Improvement of Glucose Tolerance in Zucker Diabetic Fatty Rats By Long-term Treatment With the Dipeptidyl Peptidase Inhibitor P32/98: Comparison With and Combination With Rosiglitazone." Diabetes, Obesity & Metabolism, vol. 7, no. 2, 2005, pp. 170-81.
Wargent E, Stocker C, Augstein P, et al. Improvement of glucose tolerance in Zucker diabetic fatty rats by long-term treatment with the dipeptidyl peptidase inhibitor P32/98: comparison with and combination with rosiglitazone. Diabetes Obes Metab. 2005;7(2):170-81.
Wargent, E., Stocker, C., Augstein, P., Heinke, P., Meyer, A., Hoffmann, T., Subramanian, A., Sennitt, M. V., Demuth, H. U., Arch, J. R., & Cawthorne, M. A. (2005). Improvement of glucose tolerance in Zucker diabetic fatty rats by long-term treatment with the dipeptidyl peptidase inhibitor P32/98: comparison with and combination with rosiglitazone. Diabetes, Obesity & Metabolism, 7(2), 170-81.
Wargent E, et al. Improvement of Glucose Tolerance in Zucker Diabetic Fatty Rats By Long-term Treatment With the Dipeptidyl Peptidase Inhibitor P32/98: Comparison With and Combination With Rosiglitazone. Diabetes Obes Metab. 2005;7(2):170-81. PubMed PMID: 15715890.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Improvement of glucose tolerance in Zucker diabetic fatty rats by long-term treatment with the dipeptidyl peptidase inhibitor P32/98: comparison with and combination with rosiglitazone. AU - Wargent,E, AU - Stocker,C, AU - Augstein,P, AU - Heinke,P, AU - Meyer,A, AU - Hoffmann,T, AU - Subramanian,A, AU - Sennitt,M V, AU - Demuth,H-U, AU - Arch,J R S, AU - Cawthorne,M A, PY - 2005/2/18/pubmed PY - 2005/6/10/medline PY - 2005/2/18/entrez SP - 170 EP - 81 JF - Diabetes, obesity & metabolism JO - Diabetes Obes Metab VL - 7 IS - 2 N2 - AIM: The aim of this study was to investigate the effect of long-term treatment with the dipeptidyl peptidase inhibitor P32/98 and its combination with rosiglitazone on blood glucose control and islet of Langerhans histology in male Zucker diabetic fatty (ZDF) rats, when treatment begins before or after the development of overt diabetes. METHODS: ZDF rats were treated with P32/98 from the age of 9, 12 or 15 weeks. Rosiglitazone maleate was given to a separate group from the age of 13 weeks. P32/98 was given to all of these rosiglitazone-treated rats from 16 weeks of age. Rosiglitazone maleate was also given from 16 weeks of age to half the rats that were given P32/98 from 9 weeks of age. The compounds were given by oral gavage until the rats were 14 weeks old and then in the diet. The experiment was terminated at the age of 20-21 weeks. Blood glucose, plasma insulin and oral glucose tolerance were measured at intervals; islet histology was assessed terminally. RESULTS: P32/98 improved glucose tolerance after both single and multiple doses when treatment started at 9 weeks of age, also after the third week of treatment when treatment began at 12 or 15 weeks of age. P32/98 reduced daytime blood glucose when treatment began at 12 weeks. Treatment with rosiglitazone increased food intake and body weight, and after 2 weeks, reduced daytime blood glucose, water intake and the area under the glucose tolerance curve. A single dose of P32/98 markedly improved glucose tolerance in rosiglitazone-treated rats. When treatment had begun at 9 weeks of age, P32/98 stimulated insulin secretion in some glucose tolerance tests. Neither P32/98 nor rosiglitazone affected pancreatic insulin content, nor did they have clear effects on islet histology. CONCLUSION: P32/98 elicited a sustained improvement in glucose tolerance in both prediabetic and diabetic ZDF rats. The effects of P32/98 on glucose and insulin were similar to those of rosiglitazone, and in contrast to rosiglitazone, P32/98 did not increase food intake or body weight. However, neither compound was especially effective at improving diabetes in ZDF rats when treatment began at 9, 12 or 15 (P32/98) or 13 (rosiglitazone) weeks of age. SN - 1462-8902 UR - https://www.unboundmedicine.com/medline/citation/15715890/Improvement_of_glucose_tolerance_in_Zucker_diabetic_fatty_rats_by_long_term_treatment_with_the_dipeptidyl_peptidase_inhibitor_P32/98:_comparison_with_and_combination_with_rosiglitazone_ L2 - https://doi.org/10.1111/j.1463-1326.2004.00383.x DB - PRIME DP - Unbound Medicine ER -