Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Dec 6:9:154.
doi: 10.1186/1477-7827-9-154.

Short- and long-term reproductive effects of prenatal and lactational growth restriction caused by maternal diabetes in male rats

Affiliations

Short- and long-term reproductive effects of prenatal and lactational growth restriction caused by maternal diabetes in male rats

Elaine M P Amorim et al. Reprod Biol Endocrinol. .

Abstract

Background: A suboptimal intrauterine environment may have a detrimental effect on gonadal development and thereby increases the risk for reproductive disorders and infertility in adult life. Here, we used uncontrolled maternal diabetes as a model to provoke pre- and perinatal growth restriction and evaluate the sexual development of rat male offspring.

Methods: Maternal diabetes was induced in the dams through administration of a single i.v. dose of 40 mg/kg streptozotocin, 7 days before mating. Female rats presenting glycemic levels above 200 mg/dL after the induction were selected for the experiment. The male offspring was analyzed at different phases of sexual development, i.e., peripuberty, postpuberty and adulthood.

Results: Body weight and blood glucose levels of pups, on the third postnatal day, were lower in the offspring of diabetic dams compared to controls. Maternal diabetes also provoked delayed testicular descent and preputial separation. In the offspring of diabetic dams the weight of reproductive organs at 40, 60 and 90 days-old was lower, as well as sperm reserves and sperm transit time through the epididymis. However the plasma testosterone levels were not different among experimental groups.

Conclusions: It is difficult to isolate the effects directly from diabetes and those from IUGR. Although the exposure to hyperglycemic environment during prenatal life and lactation delayed the onset of puberty in male rats, the IUGR, in the studied model, did not influenced the structural organization of the male gonads of the offspring at any point during sexual development. However the decrease in sperm reserves in epididymal cauda and the acceleration in sperm transit time in this portion of epididymis may lead to an impairment of sperm quality and fertility potential in these animals. Additional studies are needed in attempt to investigate the fertility of animals with intrauterine growth restriction by maternal diabetes and possible multigenerational effects.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Testosterone levels. Plasma testosterone levels in the animals at the age 40 days (OC, n = 5; OD, n = 5), 60 days (OC, n = 7; OD, n = 6) and 90 days (OC, n = 11; OD, n = 8). OC: offspring of control dams; OD: offspring of diabetic dams. Values expressed as mean ± SEM. Student's t-test.

Similar articles

Cited by

References

    1. Bautista CJ, Boeck L, Larrea F, Nathanielsz PW, Zambrano E. Effects of a maternal low protein isocaloric diet on milk leptin and progeny serum leptin concentration and appetitive behavior in the first 21 days of neonatal life in the rat. Pediatr Res. 2008;63(4):358–363. doi: 10.1203/01.pdr.0000304938.78998.21. - DOI - PubMed
    1. Ojeda NB, Grigore D, Alexander BT. Intrauterine growth restriction: fetal programming of hypertension and kidney disease. Adv Chronic Kidney Dis. 2008;15(2):101–106. doi: 10.1053/j.ackd.2008.01.001. - DOI - PMC - PubMed
    1. Eriksson JG, Forsén TJ, Kajantie E, Osmond C, Barker DJ. Childhood growth and hypertension in later life. Hypertension. 2007;49(6):1415–1421. doi: 10.1161/HYPERTENSIONAHA.106.085597. - DOI - PubMed
    1. Thapar A, Harold G, Rice F, Ge X, Boivin J, Hay D, Van Den Bree M, Lewis A. Do intrauterine or genetic influences explain the foetal origins of chronic disease? A novel experimental method for disentangling effects. BMC Med Res Methodol. 2007;22:7–25. - PMC - PubMed
    1. Hng TM, Cheung NW, McLean M. Growth hormone and cortisol dynamic function in relation to birth weight: a study in adult twins. J Clin Endocrinol Metab. 2005;90(5):2781–2786. doi: 10.1210/jc.2004-2497. - DOI - PubMed

Publication types

MeSH terms