Skip to main content
Log in

Oxygen diffusive conductance in placentae from control and diabetic women

  • Originals
  • Published:
Diabetologia Aims and scope Submit manuscript

Summary

Random tissue sections of placentae from control and diabetic deliveries were analysed stereologically. The aim was to test whether or not adaptations in oxygen diffusive conductances occur to help compensate for fetal hypoxic stress in utero. Organs were from 34 control and 55 diabetic deliveries (39 from White's classes A, B, C and 16 from classes D, F/R) arranged in two major groups (ABC and DFR). Tissue samples were fixed in formalin and processed for wax histology. Stereological and physicochemical quantities were used to calculate the partial conductances of six tissue layers, viz. maternal erythrocytes and plasma, villous trophoblast, villous stroma, fetal plasma and fetal erythrocytes. From partial conductances and birthweights, total and specific conductances for each placenta were determined. No differences were detected between diabetic placentae in different classes (A, B, C, D, F/R). However, both the ABC and DFR groups of diabetic placentae had higher total diffusive conductances than control organs. The increase was in the order of 7–25% and persisted even when adjustments were made for apparent differences in birthweights. The principal contributors to these changes were the post-trophoblastic (fetally located) tissue layers. These findings suggest that the diabetic placenta adapts to facilitate the diffusion of oxygen across the placenta and, thereby, to assist the hypoxic fetus.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Widness JA, Susa JB, Garcia JF et al. (1981) Increased erythropoiesis and elevated erythropoietin in infants born to diabetic mothers and in hyperinsulinemic Rhesus fetuses. J Clin Invest 67:637–642

    CAS  PubMed  Google Scholar 

  2. Carson BS, Philipps AF, Simmons MA, Battaglia FC, Meschia G (1980) Effects of a sustained insulin infusion upon glucose uptake and oxygenation of the ovine fetus. Pediatr Res 14:147–152

    CAS  PubMed  Google Scholar 

  3. Philipps AF, Dubin JW, Matty PJ, Raye JR (1982) Arterial hypoxemia and hyperinsulinemia in the chronically hyperglycemic fetal lamb. Pediatr Res 16:653–658

    CAS  Google Scholar 

  4. Philipps AF, Rosenkrantz TS, Raye J (1985) Consequences of perturbations of fetal fuels in ovine pregnancy. Diabetes 34 [Suppl 2]:32–35

    PubMed  Google Scholar 

  5. Widness JA, Teramo KA, Clemons GK et al. (1990) Direct relationship of antepartum glucose control and fetal erythropoietin in human type 1 (insulin-dependent) diabetic pregnancy. Diabetologia 33:378–383

    Article  CAS  PubMed  Google Scholar 

  6. Jones CP, Fox H (1976) An ultrastructural and ultrahistochemical study of the placenta of the diabetic woman. J. Pathol 119: 91–99

    Article  CAS  PubMed  Google Scholar 

  7. Teasdale F (1981) Histomorphometry of the placenta of the diabetic women: class A diabetes mellitus. Placenta 2:241–252

    CAS  PubMed  Google Scholar 

  8. Teasdale F (1983) Histomorphometry of the human placenta in class B diabetes mellitus. Placenta 4:1–12

    CAS  PubMed  Google Scholar 

  9. Teasdale F (1985) Histomorphometry of the human placenta in class C diabetes mellitus. Placenta 6:69–82

    CAS  PubMed  Google Scholar 

  10. Björk O, Persson B (1982) Placental changes in relation to the degree of metabolic control in diabetes mellitus. Placenta 3:367–378

    PubMed  Google Scholar 

  11. Björk O, Persson B (1984) Villous structure in different parts of the cotyledon in placentas of insulin-dependent diabetic women. A morphometric study. Acta Obstet Gynecol Scand 63: 37–43

    PubMed  Google Scholar 

  12. Mayhew TM, Sørensen FB, Klebe JG, Jackson MR (1993) Parenchymal compartments of the human placenta and the effects of maternal diabetes, mode of delivery and sex of neonate. J Anat (in press)

  13. Hirota K (1964) Electron microscopic observations on the human placenta in maternal diabetes. Fed Proc 23:575

    Google Scholar 

  14. Okudara Y (1966) Ultrastructure of the human placenta in maternal diabetesmellitus. Lab Invest 15:910–926

    Google Scholar 

  15. Jones CP, Fox H (1976) Placental changes in gestational diabetes. An ultrastructural study. Obstet Gynecol 48:274–280

    CAS  PubMed  Google Scholar 

  16. Mayhew TM, Joy CF, Haas JD (1984) Structure-function correlation in the human placenta: the morphometric diffusing capacity for oxygen at full term. J. Anat 139:691–708

    PubMed  Google Scholar 

  17. Mayhew TM, Jackson MR, Haas JD (1990) Oxygen diffusive conductances of human placentae from term pregnancies at low and high altitudes. Placenta 11:493–503

    CAS  PubMed  Google Scholar 

  18. Mayhew TM, Jackson MR, Boyd PA (1993) Changes in oxygen diffusive conductances of human placentae during gestation (10–41 weeks) are commensurate with the gain in fetal weight. Placenta 14:51–61

    CAS  PubMed  Google Scholar 

  19. Mayhew TM (1992a) The structural basis of oxygen diffusion in the human placenta. In: Egginton S, Ross HF (eds) Oxygen transport in biological systems: modelling of pathways from environment to cell. Society for Experimental Biology Seminar Series, Volume 51. Cambridge University Press, Cambridge, pp 79–101.

    Google Scholar 

  20. White P (1949) Pregnancy complicating diabetes. Am J Med 7: 609–616.

    Article  CAS  PubMed  Google Scholar 

  21. Klebe JG, Ingomar CJ (1974) Placental transfusion in infants of diabetic mothers elucidated by placental residual blood volume. Acta Paediat Scand 63:59–64

    CAS  PubMed  Google Scholar 

  22. Jackson MR, Mayhew TM, Haas JD (1987a) The volumetric composition of human term placentae: altitudinal, ethnic and sex differences in Bolivia. J Anat 152:173–187

    CAS  PubMed  Google Scholar 

  23. Jackson MR, Mayhew TM, Haas JD (1987b) Morphometric studies on villi in human term placentae and the effects of altitude, ethnic grouping and sex of newborn. Placenta 8:487–495

    CAS  PubMed  Google Scholar 

  24. Jackson MR, Mayhew TM, Haas JD (1988a) On the factors which contribute to thinning of the villous membrane in human placentae at high altitude. I. Thinning and regional variation in thickness of trophoblast. Placenta 9:1–8

    CAS  PubMed  Google Scholar 

  25. Jackson MR, Mayhew TM, Haas JD (1988b) On the factors which contribute to thinning of the villous membrane in human placentae at high altitude. II. An increase in the degree of peripheralization of fetal capillaries. Placenta 9:9–18.

    CAS  PubMed  Google Scholar 

  26. Gundersen HJG, Jensen EB (1987) The efficiency of systematic sampling in stereology and its prediction. J Microsc 147:229–263

    PubMed  Google Scholar 

  27. Stringer BMJ, Wynford-Thomas D, Williams ED (1982) Physical randomization of tissue architecture: an alternative to systematic sampling. J Microsc 126:179–182

    CAS  PubMed  Google Scholar 

  28. Bancroft JD, Cook HC (1984) Manual of histological techniques. Churchill Livingstone, Edinburgh

    Google Scholar 

  29. Mayhew TM, Jackson MR, Haas JD (1986) Microscopical morphology of the human placenta and its impact on oxygen diffusion: a morphometric model. Placenta 7:121–131

    CAS  PubMed  Google Scholar 

  30. Jackson MR, Joy CF, Mayhew TM, Haas JD (1985) Stereological studies on the true thickness of the villous membrane in human term placentae: a study of placentae from high-altitude pregnancies. Placenta 6:249–258

    CAS  PubMed  Google Scholar 

  31. Mayhew TM (1992b) A review of recent advances in stereology for quantifying neural structure. J Neurocytol 21:313–328

    Article  CAS  PubMed  Google Scholar 

  32. Weibel ER (1984) The pathway for oxygen. Harvard University Press, Cambridge

    Google Scholar 

  33. Mayhew TM, Burton GJ (1988) Methodological problems in placental morphometry: apologia for the use of stereology based on sound sampling practice. Placenta 9:565–581

    CAS  PubMed  Google Scholar 

  34. Sokal RR, Rohlf FJ (1981) Biometry. The principles and practice of statistics in biological research. WH Freeman, San Francisco

    Google Scholar 

  35. Burstein R, Bernes AW, Hirata Y, Blumenthal HT (1963) A comparative histo- and immuno-pathological study of the placenta in diabetes mellitus and in erythroblastosis fetalis. Am. J Obstet Gynecol 86:66–76

    CAS  PubMed  Google Scholar 

  36. Aladjem S (1967) Morphologic aspects of the placenta in gestational diabetes seen by phase-contrast microscopy. Am J Obstet Gynecol 99:341–349

    CAS  PubMed  Google Scholar 

  37. Aherne W, Dunnill MS (1966) Quantitative aspects of placental structure. J Path Bact 91:123–129

    CAS  PubMed  Google Scholar 

  38. Boyd PA, Scott A, Keeling JW (1986) Quantitative structural studies on placentas from pregnancies complicated by diabetes mellitus. Br J Obstet Gynaecol 93:31–35

    CAS  PubMed  Google Scholar 

  39. Moore LG, Jahnigen D, Rounds SS, Reeves JT, Grover RF (1982) Maternal hyperventilation helps preserve arterial oxygenation during high-altitude pregnancy. J Appl Physiol 52: 690–694

    CAS  PubMed  Google Scholar 

  40. Laga EM, Driscoll SG, Munro HN (1973) Quantitative studies of human placenta. I. Morphometry. Biol. Neonate 23:231–259

    CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mayhew, T.M., Sørensen, F.B., Klebe, J.G. et al. Oxygen diffusive conductance in placentae from control and diabetic women. Diabetologia 36, 955–960 (1993). https://doi.org/10.1007/BF02374479

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02374479

Key words

Navigation