Maternal diabetes affects cell proliferation in developing rat placenta

Histology and Histopathology

Volumn 26, Issue 8, 2011, Pages 1049-1056

  Zorn, T M T ^a   Zuniga M ^c   Madrid, E ^c   Tostes, R ^a   Fortes, Z ^a   Giachini, F ^a   Martín, S San ^b,c  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b Centro Regional de Estudios en Alimentos Saludables Valparaiso   (Chile)

^c UNIVERSIDAD DE VALPARAÍSO   (Chile)

Author keywords

Cell proliferation; Diabetes; Ki67; Placenta; Pregnancy; Rats; Trophoblast

Indexed keywords

BIOLOGICAL MARKER; KI 67 ANTIGEN;

ANIMAL; ARTICLE; CELL PROLIFERATION; ENZYME IMMUNOASSAY; EXPERIMENTAL DIABETES MELLITUS; FEMALE; FETOMATERNAL TRANSFUSION; METABOLISM; ORGAN SIZE; PATHOLOGY; PHYSIOLOGY; PLACENTA; PREGNANCY; PREGNANCY DIABETES MELLITUS; RAT; REPRODUCTION; WISTAR RAT;

ANIMALS; BIOLOGICAL MARKERS; CELL PROLIFERATION; DIABETES MELLITUS, EXPERIMENTAL; FEMALE; IMMUNOENZYME TECHNIQUES; KI-67 ANTIGEN; MATERNAL-FETAL EXCHANGE; ORGAN SIZE; PLACENTA; PLACENTATION; PREGNANCY; PREGNANCY IN DIABETICS; RATS; RATS, WISTAR;

MAMMALIA; RATTUS; RATTUS NORVEGICUS;

EID: 80053283203     PISSN: 02133911     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (37)

1. Acar N., Turkay Korgun E., Cayli S., Sahin Z., Demir R. and Ustunel I. (2008). Is there a relationship between PCNA expression and diabetic placental development during pregnancy?. Acta Histochem. 110, 408-417.
2. Aerts L., Holemans K. and van Assche F.A. (1990). Maternal diabetes during pregnancy: consequences for the offspring. Diabetes Metab. Rev. 6, 147-167.
3. Cassady G. (1981). The small-for-date infant. In: Neonatology: Pathophysiology and management of the newborn. Avery G.B. (ed). Lippincott. Philadelphia. pp 262-286.
4. Chartrel N.C., Clabaut M.T., Boismare F.A. and Schrub J.C. (1990). Uteroplacental hemodynamic disturbances in establishment of fetal growth retardation in streptozocin-induced diabetic rats. Diabetes 39, 743-746.
5. Curcio F. and Ceriello A. (1992). Decreased cultured endothelial cell proliferation in high glucose medium is reversed by antioxidants: new insights on the pathophysiological mechanisms of diabetic vascular complications. In Vitro Cell Dev. Biol. 28A, 787-790.
6. Daskalakis G., Marinopoulos S., Krielesi V., Papapanagiotou A., Papantoniou N., Mesogitis S. and Antsaklis A. (2008). Placental pathology in women with gestational diabetes. Acta Obstet. Gynecol. Scand. 87, 403-407.
7. Davies J. and Glasser S.R. (1968). Histological and fine structural observations on the placenta of the rat. Acta Anat. 69, 542-608.
8. de Rijk E.P., van Esch E. and Flik G. (2002). Pregnancy dating in the rat: placental morphology and maternal blood parameters. Toxicol. Pathol. 30, 271-82.
9. Desoye G. and Shafrir E. (1996). The human placenta in diabetic pregnancy. Diabetes Rev. 4, 70-89.
10. Diamant Y.Z. (1991). The human placenta in diabetes mellitus. (1991). Isr. J. Med. Sci. 27, 493-497.
11. Donath M.Y., Gross D.J., Cerasi E. and Kaiser N. (1999). Hyperglycemia-Induced cell apoptosis in pancreatic islets of Psammomys obesus during development of diabetes. Diabetes 48, 738-744.
12. Evers I.M., Nikkels P.G., Sikkema J.M. and Visser G.H. (2003). Placental pathology in women with type 1 diabetes and in a control group with normal and large-for-gestational-age infants. Placenta 24, 819-825.
13. Gewolb I.H., Merdian W., Warshaw J.B. and Enders A.C. (1986). Fine structural abnormalities of the placenta in diabetic rats. Diabetes 35, 1254-61.
14. Giachini F.R., Carriel V., Capelo L.P., Tostes R.C., Carvalho M.H., Fortes Z.B., Zorn T.M. and San Martin S. (2008). Maternal diabetes affects specific extracellular matrix components during placentation. J. Anat. 212, 31-41.
15. Heinonen S., Taipale P. and Saarikoski S. (2001). Weights of placentae from small-for-gestational age infants revisited. Placenta 22, 399-404.
16. Husain S.M., Frost R. and Mughal Z.M. (2001). Effect of diabetes mellitus on rat placenta cellularity. Early Hum. Dev. 3, 207-14.
17. Iguchi T., Tani N., Sato T., Fukatsu N. and Ohta Y. (1993). Developmental changes in mouse placental cells from several stages of pregnancy in vivo and in vitro. Biol. Reprod. 48, 188-196.
18. Kamal K., Du W., Mills I. and Sumpio B.E. (1998). Antiproliferative effect of elevated glucose in human microvascular endothelial cells. J. Cell. Biochem. 71, 491-501
19. Kim Y.H., Ryu J.M., Lee Y.J. and Han H.J. (2010). Fibronectin synthesis by high glucose level mediated proliferation of mouse embryonic stem cells: Involvement of ANG II and TGF-beta1. J. Cell Physiol. 223, 397-407.
20. Kuki S., Imanishi T., Kobayashi K., Matsuo Y., Obana M. and Akasaka T. (2006). Hyperglycemia Accelerated Endothelial Progenitor Cell Senescence via the Activation of p38 Mitogen-Activated Protein Kinase. Circulation J. 70, 1076-1081.
21. Lao T.T., Lee C.P. and Wong W.M. (1997). Placental weight to birth weight ratio is increased in mild gestational glucose intolerance. Placenta 18, 227-230.
22. Lange C., Jeruschke K., Herberg L., Leiter E.H. and Junger E. (2006). The diabetes-prone nzo/hl strain. Proliferation capacity of beta cells in hyperinsulinemia and hyperglycemia. Arch. Physiol. Biochem. 112, 49-58.
23. Larger E., Marre M., Corvol P. and Gasc J.M. (2004). Hyperglycemiainduced defects in angiogenesis in the chicken chorioallantoic membrane model. Diabetes 53, 752-761.
24. Liu W., Schoenkerman A. and Lowe W.L. Jr. (2000). Activation of members of the mitogen-activated protein kinase family by glucose in endothelial cells. Am. J. Physiol. Endocrinol. Metab. 279, E782-E790.
25. Matt D.W. and Macdonald G.J. (1985). Placental steroid production by the basal and labyrinth zones during the latter third of gestation in the rat. Biol. Reprod. 32, 969-977.
26. Molteni R.A., Stys S.J. and Battaglia F.C. (1978). Relationship of fetal and placental weight in human beings: fetal/placental weight ratio at various gestational ages and birth weight distribution. J. Reprod. Med. 21, 327-334.
27. Morisaki N., Watanabe S., Fukuda K. and Saito Y. (1999). Angiogenic interaction between retinal endothelial cells and pericytes from cells. Cell. Mol. Biol. 45, 67-77.
28. Naeye R.L. (1987). Do placental weights have clinical significance? Hum. Pathol. 18, 387-391.
29. Padmanabhan R. and Al-Zuhair A.G.H. (1990). Ultrastructural studies on the placentae of streptozotocin induced maternal diabetes in the rat. Z. Mikrosk. Anat. Forsch.104, 212-230.
30. Robinson J., Canavan J.P., El Haj A.J. and Goldspink D.F. (1988). Maternal diabetes in rats. I. Effects on placental growth and protein turnover. Diabetes 37, 1665-1670.
31. Rymaszewski Z., Szymanski P.T., Abplanalp W.A., Myatt L., Di Salvo J. and Cohen R.M. (1992). Human retinal vascular cells differ from umbilical cells in synthetic functions and their response to glucose. Proc. Soc. Exp. Biol. Med. 199, 183-191.
32. Sank A., Wei D., Reid J., Ertl D., Nimni M., Weaver F., Yellin A. and Tuan T.L. (1994). Human endothelial cells are defective in diabetic vascular disease. J. Surg. Res. 57, 647-653.
33. Suba Z. and Ujpál M. (2006). Correlations of insulin resistance and neoplasms. Magy Onkol. 50, 127-35.
34. Varma S., Lal B.K., Zheng R., Breslin J.W., Saito S., Pappas P.J., Hobson R.W. 2nd and Durán W.N. (2005). Hyperglycemia alters PI3k and Akt signaling and leads to endothelial cell proliferative dysfunction. Am. J. Physiol. Heart. Circ. Physiol. 289, H1744- H1751.
35. Weiss U., Cervar M., Puerstner P., Schmut O., Haas J., Mauschitz R., Arikan G. and Desoye G. (2001). Hyperglycemia in vitro alters proliferation and mithocondrial activity of the choriocarcinoma cell line BeWo, JAR, and JEG-3 as models for human first-trimester trophoblast. Diabetologia 44, 209-219.
36. Winick M. and Noble A. (1967). Cellular growth in human placenta. II Diabetes mellitus. Pediatrics 71, 1216-1219.
37. Younes B., Baez-Giangreco A., al-Nuaim L., al-Hakeem A. and Abu Talib Z. (1996). Basement membrane thickening in the placentae from diabetic women. Pathol. Int. 46, 100-104.