Abstract
Pregnancy stimulates DNA synthesis in uterine artery smooth muscle cells. Unknown is whether DNA synthesis increases in all layers of the vessel wall in uterine or nonuterine vessels, the distribution and time course of the proliferative response in relation to the rise in uterine blood flow, and the extent to which a pregnancy-induced rise in DNA synthesis can be mimicked by chronic estradiol treatment. To measure DNA synthesis, we implanted bromodeoxyuridine (BrdU, 400 mg) s.c. for 14-d periods in three nonpregnant, nine pregnant, three vehicle, and five estradiol (2.5 mg/14 d)-treated guinea pigs. Uterine blood flow was measured in four nonpregnant and 18 pregnant animals using radiolabeled microspheres. Pregnancy stimulated DNA synthesis in the adventitia, media, and intima of the uterine artery, radial artery (the vessels deriving from the main uterine artery and entering the uterine wall), and uterine vein but not in the aorta or mesenteric artery. Maximal uterine artery medial area and labeling indices in all layers of the uterine artery, uterine vein, and the radial artery adventitia were attained by mid-pregnancy(d 28-42 of the guinea pig's 63-day gestation), whereas DNA synthesis increased progressively until term in the radial artery media and intima. The greatest rise in uterine artery blood flow (y) occurred after peak proliferation in the uterine artery and in concert with radial artery medial and intimal proliferation (y = 1.99·100.023x where x is day postconception). 17β-Estradiol treatment for 14 d in ovariectomized guinea pigs increased DNA synthesis in the radial artery adventitia and tended (p = 0.08) to increase labeling indices in the media of all vessels examined but did not fully reproduce the effects of pregnancy. We concluded that pregnancy-related, possibly hormonal stimuli prompted growth in all layers of the uterine artery wall by mid-pregnancy and served to initiate a rise in uterine blood flow. The resultant increase in flow and shear stress likely stimulated DNA synthesis in the radial artery which helped sustain the rise in flow near term.
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Abbreviations
- BrdU:
-
bromodeoxyuridine
- PDGF:
-
platelet-derived growth factor
- Pext:
-
external perimeter of the vessel media
- Pint:
-
internal perimeter of the vessel media
References
Ramsey, EM 1973 Placental vasculature and circulation. In: Handbook of Physiology: Endocrinology, Sect 7, Vol II, Part 2. American Physiological Society, Washington DC, pp 323–337
Annibale DJ, Rosenfeld CR, Stull JT, Damm KE 1990 Protein content and myosin light chain phosphorylation in uterine artery during pregnancy. Am J Physiol 259:C484–C489
Cipolla M, Osol G 1994 Hypertrophic and hyperplastic effects of pregnancy on the rat uterine arterial wall. Am J Obstet Gynecol 171: 805–811
Griendling KK, Fuller EO, Cox RH 1985 Pregnancy induced changes in sheep uterine and carotid arteries. Am J Physiol 248:H658–H665
Makinoda S, Moll W 1986 Deoxyribonucleic acid synthesis in mesometrial arteries of guinea pig during oestrous cycle, pregnancy and treatment with oestradiol benzoate. Placenta 7: 189–198
Dempsey EC, Stevens T, Durmowicz AG, Stenmark KR 1996 Hypoxia-induced changes in contraction, growth, and matrix synthetic properties of pulmonary vascular cells. In: Haddad G, Lister G (eds) Tissue Oxygen Deprivation: Developmental, Molecular and Integrated Function, Ch 9. Marcel Dekker, New York, pp 225–274
Stenmark KR, Fasules J, Voelkel NF, Henson J, Tucker A, Wilson H, Reeves JT 1987 Severe pulmonary hypertension and arterial adventitial changes in newborn calves at 4300 m. J Appl Physiol 62: 821–830
Danforth DN, Manalo-Estrella P, Buckingham JC 1964 The effects of pregnancy and of Enovid on the rabbit vasculature. Am J Obstet Gynecol 88: 952–962
Hull AD, Long DM, Longo LC, Pierce WJ 1992 Pregnancy-induced changes in ovine cerebral arteries. Am J Physiol 262:R137–R1443
Keyes LE, Moore LG, Walchak SJ, Dempsey EC 1996 Pregnancy stimulated growth of vascular smooth muscle cells: importance of protein kinase C-dependent synergy between estrogen and platelet-derived growth factor. J Cell Physiol 166: 22–32
Palmer SK, Zamudio S, Coffin C, Parker S, Stamm E, Moore LG 1992 Quantitative estimation of human uterine artery blood flow and pelvic blood flow redistribution in pregnancy. Obstet Gynecol 80: 1000–1006
Mol W, Espach R, Wrobel KH 1983 Growth of mesometrial arteries in guinea pigs during pregnancy. Placenta 4: 111–124
Mulvany JJ 1992 Vascular growth in hypertension. J Cardiovasc Pharmacol 20( suppl 1): s7–11
Brosens IA, Robertson WB, Dixon HG 1972 The role of the spiral arteries in the pathogenesis of pre-eclampsia. Obstet Gynecol Ann 1: 177–191
Zamudio S, Palmer SK, Droma T, Stamm E, Coffin C, Moore LG 1995 Effect of altitude on uterine artery blood flow during normal pregnancy. J Appl Physiol 79: 7–14
Sugihara H, Hattore T, Fukuda M 1986 Immunohistochemical detection of bromodeoxyuridine in formalin-fixed tissues. Histochemistry 85: 193–195
Curran-Everett D, Morris KG, Moore LG 1991 Regional circulatory contributions to the increased systemic vascular conductance of pregnancy. Am J Physiol 261:H1842–H1847
Steel RGD, Torrie JH 1960 Principles and Procedures of Statistics. McGraw Hill, New York
Harrison GL, Moore LG 1989 Blunted vasoreactivity in pregnant guinea pigs is not restored by meclofenamate. Am J Obstet Gynecol 160: 258–264
Magness RR, Ford SP 1982 Steroid concentrations in uterine lymph and uterine arterial plasma of gilts during the estrous cycle and early pregnancy. Biol Reprod 27: 871–877
Conrad KP, Joffe GM, Kruszyna H, Kruszyna R, Rochelle LG, Smith RP, Chavez JE, Mosher MD 1993 Identification of increased nitric oxide biosynthesis during pregnancy in rats. FASEB J 7: 566–571
Weiner CP, Liu KZ, Thompson L, Herrig J, Chestnut D 1991 Effect of pregnancy on endothelium and smooth muscle: their role in reduced adrenergic sensitivity. Am J Physiol 261:H1275–H1283
Nakaki T, Nakayama M, Kato R 1990 Inhibition by nitric oxide and nitric oxide-producing vasodilators of DNA synthesis in vascular smooth muscle cells. Eur J Pharmacol 189: 347–353
Myers SA, Sparks JW, Makowski EL, Meschia G, Battaglia FC 1982 Relationship between placental blood flow and placental and fetal size in guinea pig. Am J Physiol 243:H404–H409
Acknowledgements
The authors thank Gene McCullough and Rebecca Dyckes for their technical assistance and Dr. Kurt Stenmark for thoughtful discussions on vascular remodeling and guidance with BrdU techniques.
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Supported by a Yale University School of Medicine Outstanding Thesis Award, an AHA Medical Student Research Fellowship (L.E.K.); an ACCP Research Award, a Giles Filey Research Award, a grant from the Veterans Administration (E.C.D.); and National Institutes of Health HL 14985, NSF Grant 8919645 (L.G.M.).
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Keyes, L., Majack, R., Dempsey, E. et al. Pregnancy Stimulation of DNA Synthesis and Uterine Blood Flow in the Guinea Pig. Pediatr Res 41, 708–715 (1997). https://doi.org/10.1203/00006450-199705000-00017
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DOI: https://doi.org/10.1203/00006450-199705000-00017
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