Na⁺, K⁺-ATPase and Ca²⁺-ATPase activities in basal and microvillous syncytiotrophoblast membranes from preeclamptic human term placenta

REFERENCES

• Hung TH, Burton GJ. Hypoxia and reoxygenation: a possible mechanism for placental oxidative stress in preeclampsia. Taiwan J Obstet Gynecol 2006;45:189–200
   PubMedGoogle Scholar
• Burton GJ, Woods AW, Jauniaux E, Kingdom JC. Rheological and physiological consequences of conversion of the maternal spiral arteries for uteroplacental blood flow during human pregnancy. Placenta 2009;30:473–82
   PubMed Web of Science ®Google Scholar
• Heazell AE, Lacey HA, Jones CJ, et al. Effects of oxygen on cell turnover and expression of regulators of apoptosis in human placental trophoblast. Placenta 2008;29:175–86
   PubMed Web of Science ®Google Scholar
• Serdar Z, Gur E, Develioglu O, et al. Placental and decidual lipid peroxidation and antioxidant defenses in preeclampsia. Lipid peroxidation in preeclampsia. Pathophysiology 2002;9:21
   PubMedGoogle Scholar
• Walsh DM, Kennedy S, Blanchflower WJ, et al. Vitamin E and selenium deficiencies increase indices of lipid peroxidation in muscle tissue of ruminant calves. Int J Vitam Nutr Res 1993;63:188–94
   PubMed Web of Science ®Google Scholar
• Hubel CA. Oxidative stress in the pathogenesis of preeclampsia. Proc Soc Exp Biol Med 1999;222:222–35
   PubMed Web of Science ®Google Scholar
• Gupta S, Agarwal A, Sharma RK. The role of placental oxidative stress and lipid peroxidation in preeclampsia. Obstet Gynecol Surv 2005;60:807–16
   PubMed Web of Science ®Google Scholar
• Hubel CA, Roberts JM, Taylor RN, et al. Lipid peroxidation in pregnancy: new perspectives on preeclampsia. Am J Obstet Gynecol 1989;161:1025–34
   PubMed Web of Science ®Google Scholar
• Casasco A, Calligaro A, Casasco M, et al. Immunohistochemical localization of lipoperoxidation products in normal human placenta. Placenta 1997;18:249–53
   PubMed Web of Science ®Google Scholar
• Morris JM, Gopaul NK, Endresen MJ, et al. Circulating markers of oxidative stress are raised in normal pregnancy and pre-eclampsia. Br J Obstet Gynaecol 1998;105:1195–9
   PubMedGoogle Scholar
• Mutlu-Turkoglu U, Aykac-Toker G, Ibrahimoglu L, et al. Plasma nitric oxide metabolites and lipid peroxide levels in preeclamptic pregnant women before and after delivery. Gynecol Obstet Invest 1999;48:247–50
   PubMed Web of Science ®Google Scholar
• Wang Y, Walsh SW. Placental mitochondria as a source of oxidative stress in pre-eclampsia. Placenta 1998;19:581–6
   PubMed Web of Science ®Google Scholar
• Ohta A, Mohri T, Ohyashiki T. Effect of lipid peroxidation on membrane-bound Ca2+-ATPase activity of the intestinal brush-border membranes. Biochim Biophys Acta 1989;984:151–7
   PubMed Web of Science ®Google Scholar
• Borrego-Díaz E, Rosales JC, Proverbio T, et al. Effect of placental hypoxia on the plasma membrane Ca-ATPase (PMCA) activity and the level of lipid peroxidation of syncytiotrophoblast and red blood cell ghosts. Placenta 2008;29:44–50
   Google Scholar
• Matteo R, Proverbio T, Córdova K, et al. Preeclampsia, lipid peroxidation, and calcium adenosine triphosphatase activity of red blood cell ghost. Am J Obstet Gynecol 1998;178:402–8
   PubMed Web of Science ®Google Scholar
• Carrera F, Casart Y, Proverbio T, et al. Preeclampsia and calcium-ATPase activity of plasma membranes from human myometrium and placental trophoblast. Hypertens Pregnancy 2003;22:295–304
   PubMed Web of Science ®Google Scholar
• Dobretsov GE, Borschevskaya TA, Petrov VA, Vladimirov YA. The increase of phospholipid bilayer rigidity after lipid peroxidation. FEBS Lett 1977;84:125–8
   PubMed Web of Science ®Google Scholar
• Le Grimellec C, Friedlander G, el Yandouzi EH, et al. Membrane fluidity and transport properties in epithelia. Kidney Int 1992;42:825–36
   PubMed Web of Science ®Google Scholar
• Kako K, Kato M, Matsuoka T, Mustapha A. Depression of membrane-bound Na+-K+-ATPase activity induced by free radicals and by ischemia of kidney. Am J Physiol 1988;254:C330–7
   Google Scholar
• Ohta A, Mohri T, Ohyashiki T. Effect of lipid peroxidation on membrane-bound Ca2+-ATPase activity of the intestinal brush-border membranes. Biochim Biophys Acta 1989;984:151–7
   PubMed Web of Science ®Google Scholar
• Casart Y, Proverbio T, Marín R, Proverbio F. Comparative study of the calcium adenosine triphosphatase of basal membranes of human placental trophoblasts from normotensive and preeclamptic pregnant women. Gynecol Obstet Invest 2001;51:28–31
   PubMed Web of Science ®Google Scholar
• Nardulli G, Proverbio F, Limongi FG, et al. Preeclampsia and calcium adenosine triphosphatase activity of red blood cell ghosts. Am J Obstet Gynecol 1994;171:1361–5
   PubMed Web of Science ®Google Scholar
• Maxwell CV, Tao QF, Seely EW, et al. Regulation of the sodium pump in pregnancy-related tissues in preeclampsia. Am J Obstet Gynecol 1998;179:28–34
   PubMed Web of Science ®Google Scholar
• Miyamoto S, Makino N, Shimokawa H, et al. The characteristics of erythrocyte Na+ transport systems in normal pregnancy and pregnancy-induced hypertension. J Hypertens 1992;10:367–72
   PubMed Web of Science ®Google Scholar
• Testa I, Rabini RA, Danieli G, et al. Abnormal membrane cation transport in pregnancy-induced hypertension. Scand J Clin Lab Invest 1988;48:7–13
   PubMed Web of Science ®Google Scholar
• Khullar S, Greenwood SL, McCord N, et al. Nitric oxide and superoxide impair human placental amino acid uptake and increase Na+ permeability: implications for fetal growth. Free Radic Biol Med 2004;36:271–7
   Google Scholar
• Johansson M, Jansson T, Powell TL. Na+-K+-ATPase is distributed to microvillous and basal membrane of the syncytiotrophoblast in human placenta. Am J Physiol 2000;279:R287–94
   PubMed Web of Science ®Google Scholar
• Marín R, Riquelme G, Godoy V, et al. Functional and structural demonstration of the presence of Ca-ATPase (PMCA) in both microvillous and basal plasma membranes from syncytiotrophoblast of human term placenta. Placenta 2008;29:671–9
   Google Scholar
• Sowers JR, Zemel MB, Bronsteen RA, et al. Erythrocyte cation metabolism in preeclampsia. Am J Obstet Gynecol 1989;161:441–5
   PubMed Web of Science ®Google Scholar
• von Dadelszen P, Wilkins T, Redman CW. Maternal peripheral blood leukocytes in normal and pre-eclamptic pregnancies. Br J Obstet Gynaecol 1999;106:576–81
   PubMedGoogle Scholar
• Haller H, Oeney T, Hanck V, et al. Increased intracellular free calcium and sensitivity to angiotensin II in platelets of preeclamptic women. Am J Hypertens 1989;2:238–43
   PubMed Web of Science ®Google Scholar
• Adair CD, Haupert GT Jr, Koh HP, et al. Erythrocyte sodium/potassium ATPase activity in severe preeclampsia. J Perinatol 2009;29:280–3
   PubMed Web of Science ®Google Scholar
• Illsley NP, Wang ZQ, Gray A, et al. Simultaneous preparation of paired, syncytial, microvillous and basal membranes from human placenta. Biochim Biophys Acta 1990;1029:218–26
   Google Scholar
• Jimenez V, Henriquez M, Llanos P, Riquelme G. Isolation and purification of human placental plasma membranes from normal and pre-eclamptic pregnancies. a comparative study. Placenta 2004;25:422–37
   Google Scholar
• Fisher GJ, Kelley LK, Smith CH. ATP-dependent calcium transport across basal plasma membranes of human placental trophoblast. Am J Physiol 1987;252:C38–46
   Google Scholar
• Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976;72:248–54
   PubMed Web of Science ®Google Scholar
• Proverbio F, Proverbio T, Marín R. Na+-ATPase is a different entity from the (Na++K+)-ATPase in rat kidney basolateral plasma membranes. Biochim Biophys Acta 1986;858:202–5
   PubMed Web of Science ®Google Scholar
• Feix JB, Bachowski GJ, Girotti AW. Photodynamic action of merocyanine 540 on erythrocyte membranes: structural perturbation of lipid and protein constituents. Biochim Biophys Acta 1991;1075:28–35
   PubMed Web of Science ®Google Scholar
• Adamo HP, Rega AF, Garrahan PJ. Magnesium-ions accelerate the formation of the phosphoenzyme of the (Ca2++Mg2+)-activated ATPase from plasma membranes by acting on the phosphorylation reaction. Biochem Biophys Res Comm 1990;169:700–5
   Google Scholar
• Clarson LH, Glazier JD, Greenwood SL, et al. Activity and expression of Na+-K+-ATPase in human placental cytotrophoblast cells in culture. J Physiol 1996;497:735–43
   Google Scholar
• Borrego E, Proverbio T, Marín R, Proverbio F. Lipid peroxidation and Ca-ATPase activity of basal plasma membranes of syncytiotrophoblast from normotensive pregnant women. Gynecol Obstet Invest 2006;61:128–32
   PubMed Web of Science ®Google Scholar
• Oviedo NJ, Benaim G, Cervino V, et al. The plasma membrane Ca2+-ATPase protein from red blood cells is not modified in preeclampsia. Biochim Biophys Acta 2006;1762:381–5
   PubMed Web of Science ®Google Scholar
• Haché S, Takser L, LeBellego F, et al. Alteration of calcium homeostasis in primary preeclamptic syncytiotrophoblasts: effect on calcium exchange in placenta. J Cell Mol Med 2011;15:654–67
   PubMedGoogle Scholar
• Moreau R, Daoud G, Masse A, et al. Expression and role of calcium-ATPase pump and sodium-calcium exchanger in differentiated trophoblasts from human term placenta. Mol Reprod Dev 2003;65:283–8
   Google Scholar
• Strehler EE, James P, Fischer R, et al. Peptide sequence analysis and molecular cloning reveal two calcium pump isoforms in the human erythrocyte membrane. J Biol Chem 1990;265:2835–42
   PubMed Web of Science ®Google Scholar
• Agunanne E, Horvat D, Harrison R, et al. Marinobufagenin levels in preeclamptic patients: a preliminary report. Am J Perinatol 2011;28:509–14
   Google Scholar
• Adair CD, Buckalew VM, Graves SW, et al. Digoxin immune fab treatment for severe preeclampsia. Am J Perinatol 2010;27:655–62
   PubMed Web of Science ®Google Scholar
• Hopoate-Sitake ML, Adair CD, Mason LA, et al. Digibind reverses inhibition of cellular Rb+ uptake caused by endogenous sodium pump inhibitors present in serum and placenta of women with preeclampsia. Reprod Sci 2011;18:190–9
   Google Scholar
• Teppa-Garrán A, Proverbio T, Marín R, Proverbio F. Lipid peroxidation and active calcium transport in inside-out vesicles of red blood cells from preeclamptic women. Int J Biochem Cell Biol 2004;36:806–13
   PubMedGoogle Scholar