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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Alterations in the structural characteristics of rectus abdominis muscles caused by diabetes and pregnancy: A comparative study of the rat model and women

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Vesentini, Giovana [1, 2] ; Barbosa, Angelica M. P. [2, 3] ; Damasceno, Debora C. [1] ; Marini, Gabriela [1, 2, 4] ; Piculo, Fernanda [1, 2] ; Matheus, Selma M. M. [5, 2] ; Hallur, Raghavendra L. S. [1, 2] ; Nunes, Sthefanie K. [1, 2] ; Catinelli, Bruna B. [1, 2] ; Magalhaes, Claudia G. [1, 2] ; Costa, Roberto [1, 2] ; Abbade, Joelcio F. [1, 2] ; Corrente, Jose E. [2, 6] ; Calderon, Iracema M. P. [1, 2] ; Rudge, Marilza V. C. [1, 2] ; Grp, DIAMATER Study
Total Authors: 16
Affiliation:
[1] Sao Paulo State Univ UNESP, Botucatu Med Sch, Dept Gynecol & Obstet, Botucatu, SP - Brazil
[2] Univ Estadual Paulista UNESP, Univ Hosp, Perinatal Diabet Res Ctr, Botucatu Med Sch, Botucatu, SP - Brazil
[3] Sao Paulo State Univ UNESP, Sch Philosophy & Sci, Dept Physiotherapy & Occupat Therapy, Marilia, SP - Brazil
[4] Univ Sagrad Coracao, Dept Hlth Sci, Bauru, SP - Brazil
[5] Sao Paulo State Univ UNESP, Inst Biosci, Dept Anat, Botucatu, SP - Brazil
[6] Sao Paulo State Univ UNESP, Biosci Inst, Dept Biostat, Botucatu, SP - Brazil
Total Affiliations: 6
Document type: Journal article
Source: PLoS One; v. 15, n. 4 APR 3 2020.
Web of Science Citations: 0
Abstract

Background and objective In the present study, we compared the effect of diabetic pregnancy on the rectus abdominis muscle (RAM) in humans and rats. We hypothesized that our animal model could provide valuable information about alterations in the RAM of women with Gestational Diabetes (GDM). Method Newborns female rats (n = 10/group) were administered streptozotocin (100 mg/kg body weight) subcutaneously and were mated on reaching adulthood, to develop the mild hyperglycemic pregnant (MHP) rat model. At the end of pregnancy, the mothers were sacrificed, and the RAM tissue was collected. Pregnant women without GDM (non-GDM group; n = 10) and those diagnosed with GDM (GDM group; n = 8) and undergoing treatment were recruited, and RAM samples were obtained at C-section. The RAM architecture and the distribution of the fast and slow fibers and collagen were studied by immunohistochemistry. Results No statistically significant differences in the maternal and fetal characters were observed between the groups in both rats and women. However, significant changes in RAM architecture were observed. Diabetes in pregnancy increased the abundance of slow fibers and decreased fast fiber number and area in both rats and women. A decrease in collagen distribution was observed in GDM women; however, a similar change was not observed in the MHP rats. Conclusion Our results indicated that pregnancy-associated diabetes-induced similar structural adaptations in the RAM of women and rats with slight alterations in fiber type number and area. These findings suggest that the MHP rat model can be used for studying the effects of pregnancy-associated diabetes on the fiber structure of RAM. (AU)

FAPESP's process: 16/09710-9 - Characterization of gestational hyperglycemia and gestational urinary incontinence markers in the prediction of urinary incontinence 6-12 months postpartum
Grantee:Marilza Vieira Cunha Rudge
Support Opportunities: Regular Research Grants
FAPESP's process: 16/01743-5 - The new gestational triad: hyperglycemia, urinary incontinence (UI) and biomolecular profile as a long-term predictor for UI: a prospective cohort study: translational research with biodevice with stem cells for muscle regeneration in diabetic rats
Grantee:Marilza Vieira Cunha Rudge
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 14/26852-6 - EFFECTS OF GESTATIONAL HYPERGLYCEMIA AND GESTATIONAL URINARY INCONTINENCE ON RECTUS ABDOMINIS MUSCLE: EXTRACELLULAR MATRIX, PROTEIN EXPRESSION AND ULTRASTRUCTURE
Grantee:Giovana Vesentini
Support Opportunities: Scholarships in Brazil - Doctorate