Literature DB >> 20127828

Cardiac malformations and alteration of TGFbeta signaling system in diabetic embryopathy.

Zhiyong Zhao1.   

Abstract

BACKGROUND: Cardiovascular defects are the most common anomalies in diabetic embryopathy. The mechanisms underlying the manifestation of the defects remain to be addressed.
METHODS: Female mice were administered streptozotocin to induce diabetes. Embryos from euglycemic (control) and hyperglycemic groups were examined for morphological and histological evaluation of malformations. Cell proliferation and programmed cell death (apoptosis) were assessed using mitotic markers (BrdU and Ki67) and TUNEL assay, respectively. Expression of eight four genes in the TGFbeta signaling system was analyzed using real-time RT-PCR.
RESULTS: Structural abnormalities were observed in the heart and neural tube in diabetic groups, with significantly higher malformation rates than in control groups. Moreover, malformation rates in the heart were higher than those in the neural tube. Cardiac abnormalities including dilated heart tube, smaller ventricles, conotruncal stenosis, and abnormal heart looping were seen during early morphogenesis prior to cardiac septation [embryonic day (E) 9.5-11.5]. Histological examinations showed hypoplastic myocardium and endocardial cushions. After cardiac septation (E15.5), ventricular septal defects were observed, which were manifested in the non-muscular portion of the septum. Significant decreases in cell proliferation with no differences in apoptosis were observed in the myocardium and endocardial cushions in diabetic compared to control groups. Factors in the TGFbeta signaling that regulate heart development were downregulated by maternal diabetes.
CONCLUSIONS: Maternal diabetes causes malformations in the heart of the embryo. The heart is more susceptible to maternal diabetic insults than the neural tube. Malformations in the heart prior to septation are associated with decreased cell proliferation, but not increased apoptosis. The TGFbeta signaling is involved in cardiac malformations in diabetic embryopathy. 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20127828     DOI: 10.1002/bdrb.20225

Source DB:  PubMed          Journal:  Birth Defects Res B Dev Reprod Toxicol        ISSN: 1542-9733


  16 in total

1.  Reduction in embryonic malformations and alleviation of endoplasmic reticulum stress by nitric oxide synthase inhibition in diabetic embryopathy.

Authors:  Zhiyong Zhao; Richard L Eckert; E Albert Reece
Journal:  Reprod Sci       Date:  2012-04-24       Impact factor: 3.060

2.  TGFβ and Wnt in cardiac outflow tract defects in offspring of diabetic pregnancies.

Authors:  Zhiyong Zhao
Journal:  Birth Defects Res B Dev Reprod Toxicol       Date:  2014-09-17

3.  GSK3β and MCL-1 mediate cardiomyocyte apoptosis in response to high glucose.

Authors:  Dongmei Su; Jing Zhao; Shanshan Hu; Lina Guan; Qian Li; Cuige Shi; Xu Ma; Jianjun Gou; Yunjun Zhou
Journal:  Histochem Cell Biol       Date:  2019-06-14       Impact factor: 4.304

4.  Oxidative stress is responsible for maternal diabetes-impaired transforming growth factor beta signaling in the developing mouse heart.

Authors:  Fang Wang; E Albert Reece; Peixin Yang
Journal:  Am J Obstet Gynecol       Date:  2015-01-13       Impact factor: 8.661

5.  Formation of neurodegenerative aggresome and death-inducing signaling complex in maternal diabetes-induced neural tube defects.

Authors:  Zhiyong Zhao; Lixue Cao; E Albert Reece
Journal:  Proc Natl Acad Sci U S A       Date:  2017-04-10       Impact factor: 11.205

Review 6.  New concepts in diabetic embryopathy.

Authors:  Zhiyong Zhao; E Albert Reece
Journal:  Clin Lab Med       Date:  2013-04-19       Impact factor: 1.935

7.  In ovo hyperglycemia causes congenital limb defects in chicken embryos via disruption of cell proliferation and apoptosis.

Authors:  Zehuan Ding; Huijuan Zhou; Naomi McCauley; Gladys Ko; Ke K Zhang; Linglin Xie
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2020-08-30       Impact factor: 5.187

Review 8.  Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms.

Authors:  Madhumita Basu; Vidu Garg
Journal:  Birth Defects Res       Date:  2018-12-01       Impact factor: 2.344

Review 9.  The role of glucose in physiological and pathological heart formation.

Authors:  Haruko Nakano; Viviana M Fajardo; Atsushi Nakano
Journal:  Dev Biol       Date:  2021-02-10       Impact factor: 3.148

10.  Hyperglycemia slows embryonic growth and suppresses cell cycle via cyclin D1 and p21.

Authors:  Devon E Scott-Drechsel; Sandra Rugonyi; Daniel L Marks; Kent L Thornburg; Monica T Hinds
Journal:  Diabetes       Date:  2012-11-27       Impact factor: 9.461

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