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Maternal Separation and Negative Renal Programming, Evidence of Morphofunctional Alterations in Rodent Models:
Jhonatan Duque-Colorado1,2, Josue Rivadeneira3,4, Bélgica Vásquez1,2,5
1Doctoral Program in Morphological Sciences, Faculty of Medicine, Universidad de La Frontera, Temuco 4811230, Chile.
Early life stress, modeled by maternal separation (MS) in rodents, persistently alters kidney structure and function. This review highlights MS-induced changes in renal cells, microvasculature, and molecular pathways, impacting kidney development.
Area of Science:
- Nephrology
- Developmental Biology
- Stress Physiology
Background:
- Early life stress is linked to long-term physiological changes, including renal system alterations.
- Maternal separation (MS) in rodents models postnatal adversity but its impact on kidney structure and function remains incompletely understood.
Purpose of the Study:
- To systematically review the effects of maternal separation (MS) on the morphofunctional characteristics of the kidney in rodent models.
- To identify structural, functional, and molecular changes in the developing kidney following MS.
Main Methods:
- Systematic review following SYRCLE and PRISMA guidelines, registered in PROSPERO.
- Searched multiple databases (Web of Science, Scopus, Medline, Embase, BIREME-BVS, SciELO) without restrictions.
- Included seven rodent studies evaluating renal structural, functional, or molecular alterations post-MS; risk of bias assessed using SYRCLE's RoB tool.
Main Results:
- Structural changes included cellular infiltrates (MPO, CD44, TLR4 positive) and increased microvascular density.
- Functional alterations involved changes in ACE1/ACE2 activity, oxidative stress, and enzymatic imbalance with a compensatory antioxidant response.
- Molecular variations observed in adrenergic receptors and renin-angiotensin system expression.
Conclusions:
- Maternal separation (MS) may compromise the organization and functional integrity of the developing kidney.
- Findings suggest a need for integrated structural and functional analyses to further elucidate MS effects on kidney development.
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