Increased Myogenic Responses of Resistance-Sized Mesenteric Arteries After Reduced Uterine Perfusion Pressure in Pregnant Rats

REFERENCES

• Gammill HS, Roberts JM. Emerging concepts in preeclampsia investigation. Front Biosci 2007; 12:2403–2411.
   PubMed Web of Science ®Google Scholar
• Lain KY, Roberts JM. Contemporary concepts of the pathogenesis and management of preeclampsia. JAMA 2002; 287:3183–3186.
   PubMed Web of Science ®Google Scholar
• Roberts JM, Taylor RN, Goldfien A. Endothelial cell activation as a pathogenetic factor in preeclampsia. Semin Perinatol 1991; 15:86–93.
   PubMed Web of Science ®Google Scholar
• Roberts JM, Taylor RN, Goldfien A. Clinical and biochemical evidence of endothelial cell dysfunction in the pregnancy syndrome preeclampsia. Am J Hypertens 1991; 4:700–708.
   PubMed Web of Science ®Google Scholar
• Roberts L, Lamarca BB, Fournier L, Bain J, Cockrell K, Granger JP. Enhanced endothelin synthesis by endothelial cells exposed to sera from pregnant rats with decreased uterine perfusion. Hypertension 2006; 47:615–618.
   PubMed Web of Science ®Google Scholar
• Ashworth JR, Warren AY, Johnson IR, Baker PN. Plasma from pre-eclamptic women and functional change in myometrial resistance arteries. Br J Obstet Gynaecol 1998; 105:459–461.
   PubMedGoogle Scholar
• Pascoal IF, Lindheimer MD, Nalbantian-Brandt C, Umans JG. Preeclampsia selectively impairs endothelium-dependent relaxation and leads to oscillatory activity in small omental arteries. J Clin Invest 1998; 101:464–470.
   PubMed Web of Science ®Google Scholar
• Chesley LC. Lindheimer M, Roberts JM, Cunningham FG, eds. Chesley's Hypertensive Disorders in Pregnancy. Stamford, CT: Appleton & Lange; 1999.
   Google Scholar
• Crews JK, Herrington JN, Granger JP, Khalil RA. Decreased endothelium-dependent vascular relaxation during reduction of uterine perfusion pressure in pregnant rat. Hypertension 2000; 35:367–372.
   PubMed Web of Science ®Google Scholar
• Alexander BT, Rinewalt AN, Cockrell KL, Massey MB, Bennett WA, Granger JP. Endothelin type a receptor blockade attenuates the hypertension in response to chronic reductions in uterine perfusion pressure. Hypertension 2001; 37:485–489.
   PubMed Web of Science ®Google Scholar
• Alexander BT, Bennett WA, Khalil RA. Reduced uterine perfusion pressure during pregnancy in the rat is associated with increases in arterial pressure and changes in renal nitric oxide. Amer J Hyperten 2001; 14:178–185S.
   Google Scholar
• Lamarca BB, Gilbert J, Granger JP. Recent progress toward the understanding of the pathophysiology of hypertension during preeclampsia. Hypertension 2008; 51:982–988.
   PubMed Web of Science ®Google Scholar
• Gilbert JS, Babcock SA, Granger JP. Hypertension produced by reduced uterine perfusion in pregnant rats is associated with increased soluble fms-like tyrosine kinase-1 expression. Hypertension 2007; 50:1142–1147.
   PubMed Web of Science ®Google Scholar
• Gilbert JS, Ryan MJ, Lamarca BB, Sedeek M, Murphy SR, Granger JP. Pathophysiology of hypertension during preeclampsia: linking placental ischemia with endothelial dysfunction. Am J Physiol Heart Circ Physiol 2008; 294:H541–550.
   PubMed Web of Science ®Google Scholar
• Gilbert J, Dukes M, Lamarca B, Cockrell K, Babcock S, Granger J. Effects of reduced uterine perfusion pressure on blood pressure and metabolic factors in pregnant rats. Am J Hypertens 2007; 20:686–691.
   PubMed Web of Science ®Google Scholar
• Anderson CM, Lopez F, Zhang HY, Pavlish K, Jn Benoit. Reduced uteroplacental perfusion alters uterine arcuate artery function in the pregnant Sprague–Dawley rat. Biol Reprod 2005; 72:762–766.
   PubMed Web of Science ®Google Scholar
• Anderson CM, Lopez F, Zhang HY, Shirasawa Y, Pavlish K, Benoit JN. Mesenteric vascular responsiveness in a rat model of pregnancy-induced hypertension. Exp Biol Med (Maywood) 2006; 231:1398–1402.
   PubMed Web of Science ®Google Scholar
• Novak J, Ramirez RJ, Gandley RE, Sherwood OD, Conrad KP. Myogenic reactivity is reduced in small renal arteries isolated from relaxin-treated rats. Am J Physiol Regul Integr Comp Physiol 2002; 283:R349–355.
   PubMed Web of Science ®Google Scholar
• Ramirez RJ, Hubel CA, Novak J, Dicianno JR, Kagan VE, Gandley RE. Moderate ascorbate deficiency increases myogenic tone of arteries from pregnant but not virgin ascorbate-dependent rats. Hypertension 2006; 47:454–460.
   PubMed Web of Science ®Google Scholar
• Novak J, Danielson LA, Kerchner LJ, Relaxin is essential for renal vasodilation during pregnancy in conscious rats. J Clin Invest 2001; 107:1469–1475.
   PubMed Web of Science ®Google Scholar
• Ramirez RJ, Novak J, Johnston TP, Gandley RE, Mclaughlin MK, Hubel CA. Endothelial function and myogenic reactivity in small mesenteric arteries of hyperlipidemic pregnant rats. Am J Physiol Regul Integr Comp Physiol 2001; 281:R1330–R1337.
   PubMed Web of Science ®Google Scholar
• Alexander BT, Llinas MT, Kruckeberg WC, Granger JP. L-arginine attenuates hypertension in pregnant rats with reduced uterine perfusion pressure. Hypertension 2004; 43:832–836.
   PubMed Web of Science ®Google Scholar
• Cockrell KL, Alexander BT, Granger JP, Khalil RA, Crews JK. Decreased endothelium-dependent vascular relaxation during reduction of uterine perfusion pressure in pregnant rat. Amer J Physiol Regulatory Integrat Comparat Physiol 2000; 278:R295–303.
   Google Scholar
• Abitbol MM. Simplified technique to produce toxemia in the rat: considerations on cause of toxemia. Clin Exp Hypertens B 1982; 1:93–103.
   PubMed Web of Science ®Google Scholar
• Rocca B, Loeb Al, Strauss JF3rd, Directed vascular expression of the thromboxane A2 receptor results in intrauterine growth retardation. Nature Med 2000; 6:219–221.
   PubMed Web of Science ®Google Scholar
• Llinas MT, Alexander BT, Seedek M, Abram SR, Crell A, Granger JP. Enhanced thromboxane synthesis during chronic reductions in uterine perfusion pressure in pregnant rats. Amer J Hyperten 2002; 15:793–797.
   PubMed Web of Science ®Google Scholar
• Llinas MT, Alexander BT, Capparelli MF, Carroll MA, Granger JP. Cytochrome P-450 inhibition attenuates hypertension induced by reductions in uterine perfusion pressure in pregnant rats. Hypertension 2004; 43:623–628.
   PubMed Web of Science ®Google Scholar
• Lamarca B, Wallukat G, Llinas M, Herse F, Dechend R, Granger JP. Autoantibodies to the angiotensin type I receptor in response to placental ischemia and tumor necrosis factor alpha in pregnant rats. Hypertension 2008; 52:1168–1172.
   PubMed Web of Science ®Google Scholar
• Lamarca BD, Alexander BT, Gilbert JS, Pathophysiology of hypertension in response to placental ischemia during pregnancy: a central role for endothelin?. Gend Med 2008; 5(Suppl A):S133–S138.
   Google Scholar
• Gadonski G, Lamarca BB, Sullivan E, Bennett W, Chandler D, Granger JP. Hypertension produced by reductions in uterine perfusion in the pregnant rat: role of interleukin 6. Hypertension 2006; 48:711–716.
   PubMed Web of Science ®Google Scholar
• Ashworth JR, Warren AY, Baker PN, Johnson IR. Loss of endothelium-dependent relaxation in myometrial resistance arteries in pre-eclampsia. Br J Obstet Gynaecol 1997; 104:1152–1158.
   PubMedGoogle Scholar
• Pascoal IF, Umans JG. Effect of pregnancy on mechanisms of relaxation in human omental microvessels. Hypertension 1996; 28:183–187.
   PubMedGoogle Scholar
• Davidge ST, Baker PN, Roberts JM. NOS expression is increased in endothelial cells exposed to plasma from women with preeclampsia. Am J Physiol 1995; 269:H1106–1112.
   PubMed Web of Science ®Google Scholar
• Davidge ST, Ap Signorella, Ca Hubel, Dl Lykins, Jm Roberts. Distinct factors in plasma of preeclamptic women increase endothelial nitric oxide or prostacyclin. Hypertension 1996; 28:758–764.
   PubMed Web of Science ®Google Scholar
• Sladek SM, Magness RR, Conrad KP. Nitric oxide and pregnancy. Am J Physiol 1997; 272:R441–463.
   PubMed Web of Science ®Google Scholar
• Davidge ST, Hubel CA, Mclaughlin MK. Lipid peroxidation increases arterial cyclooxygenase activity during pregnancy. Amer J Obstet Gynecol 1994; 170:215–222.
   PubMedGoogle Scholar
• Davidge ST, Hubel CA, Mclaughlin MK. Cyclooxygenase-dependent vasoconstrictor alters vascular function in the vitamin E-deprived rat. Circul Res 1993; 73:79–88.
   PubMedGoogle Scholar
• Davidge ST, Everson WV, Parisi VM, Mclaughlin MK. Pregnancy and lipid peroxide-induced alterations of eicosanoid-metabolizing enzymes in the aorta of the rat. Amer J Obstet Gynecol 1993; 169:1338–1344.
   PubMedGoogle Scholar
• Davidge ST. Oxidative stress and altered endothelial cell function in preeclampsia. Semin Reproduct Endocrinol 1998; 16:65–73.
   PubMedGoogle Scholar
• Tyurin VA, Liu SX, Tyurina YY, Elevated levels of S-nitrosoalbumin in preeclampsia plasma. Circ Res 2001; 88:1210–1215.
   PubMed Web of Science ®Google Scholar
• Godfrey KM, Barker DJ. Fetal programming and adult health. Public Health Nutr 2001; 4:611–624.
   PubMedGoogle Scholar
• Barker DJ. Fetal origins of cardiovascular disease. Ann Med 1999; 31:3–6.
   PubMed Web of Science ®Google Scholar
• Barker DJ. The malnourished baby and infant. Br Med Bull 2001; 60:69–88.
   PubMed Web of Science ®Google Scholar