4.7 Article

Type 2 diabetic mice have increased arteriolar tone and blood pressure - Enhanced release of COX-2-derived constrictor prostaglandins

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/01.ATV.0000172688.26838.9f

关键词

type 2 diabetes mellitus; microvessels; basal arteriolar tone; cyclooxygenase-2

资金

  1. NHLBI NIH HHS [HL-43023, HL-46813] Funding Source: Medline

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Objective-Type 2 diabetes mellitus (T2-DM) is frequently associated with vascular dysfunction and elevated blood pressure, yet the underlying mechanisms are not completely understood. We hypothesized that in T2-DM, the regulation of peripheral vascular resistance is altered because of changes in local vasomotor mechanisms. Methods and Results-In mice with T2-DM (C57BL/KsJ-db(-)/db(-)), systolic and mean arterial pressures measured by the tail cuff method were significantly elevated compared with those of control (db(+)/db(-)) animals (db/db, 146 +/- 5 and 106 +/- 2 mm Hg versus control, 133 +/- 4 and 98 +/- 4 mm Hg, respectively; P<0.05). Total peripheral resistance, calculated from cardiac output values (measured by echocardiography) and mean arterial pressure were significantly elevated in db/db mice (db/db, 25 +/- 6 versus control, 15 +/- 1 mm Hg[middot] mL(-1)[middot] min(-1)). In isolated, pressurized gracilis muscle arterioles (diameter approximate to 80 mu m) from db/db mice, stepwise increases in intraluminal pressure (from 20 to 120 mm Hg) elicited a greater reduction in diameter than in control vessels at each pressure step (at 80 mm Hg, db/db, 66 +/- 4% versus control, 79 +/- 3%). The passive diameters of arterioles (obtained in Ca2+-free solution) and the calculated myogenic index were not significantly different in the 2 groups. The presence of the prostaglandin H-2/thromboxane A(2) receptor antagonist SQ29548 did not affect arteriolar diameters of control mice but reduced the enhanced arteriolar tone of db/db mice back to control levels (at 80 mm Hg, 80 +/- 4%). The inhibitor of cyclooxygenase-1 (COX-1), SC-560, did not affect the basal tone of arterioles, whereas NS-398, an inhibitor of COX-2, caused a significant shift in the arteriolar pressure-diameter curve of vessels from db/db mice (at 80 mm Hg, 76 +/- 3%) but not in those of control mice. Also, in aortas of db/db mice, expression of COX-2 was enhanced compared with controls. Conclusions-Collectively, these findings suggest that in mice with T2-DM, the basal tone of skeletal muscle arterioles is increased because of an enhanced COX-2-dependent production of constrictor prostaglandins. These alterations in microvascular prostaglandin synthesis may contribute to the increase in peripheral resistance and blood pressure in T2-DM.

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