Activation of prostaglandin E₂ EP1 receptor increases arteriolar tone and blood pressure in mice with type 2 diabetes

Abstract

Aims

Type 2 diabetes mellitus is frequently associated with hypertension, but the underlying mechanisms are not completely understood. We tested the hypothesis that activation of type 1 prostaglandin E₂ (PGE₂) receptor (EP1) increases skeletal muscle arteriolar tone and blood pressure in mice with type 2 diabetes.

Methods and results

In 12-week-old, male db/db mice (with homozygote mutation in leptin receptor), systolic blood pressure was significantly elevated, compared with control heterozygotes. Isolated, pressurized gracilis muscle arterioles (∼90 µm) of db/db mice exhibited an enhanced pressure- and angiotensin II (0.1–10 nM)-induced tone, which was reduced by the selective EP1 receptor antagonist, AH6809 (10 µM), to the level observed in arterioles of control mice. Exogenous application of PGE₂ (10 pM–100 nM) or the selective agonist of the EP1 receptor, 17-phenyl-trinor-PGE₂ (10 pM–100 nM), elicited arteriolar constrictions that were significantly enhanced in db/db mice (max: 31 ± 4 and 29 ± 5%), compared with controls (max: 20 ± 2 and 14 ± 3%, respectively). In the aorta of db/db mice, an increased protein expression of EP1, but not EP4, receptor was also detected by western immunoblotting. Moreover, we found that oral administration of the EP1 receptor antagonist, AH6809 (10 mg/kg/day, for 4 days), significantly reduced the systolic blood pressure in db/db, but not in control mice.

Conclusion

Activation of EP1 receptors increases arteriolar tone, which could contribute to the development of hypertension in the db/db mice.

Diabetes, Hypertension, Arteriole, Prostanoid, EP receptor