Cited by 7Mesenchymal stem cell researchMenopause: Health Impacts and TreatmentsEstrogen and related hormone effects

Therapeutic Potential of Mesenchymal Stem Cells vs. Estradiol Benzoate or Avosoya on the Cerebellar Cortex of Ovariectomized Adult Albino Rats

Ahmed, Samah M, Abdelrahman, Shaimaa A, Shalaby, Sally M·2017·Journal of Cytology & Histology

Abstract

Alterations in hormone levels during menopause affect cognitive function and brain chemistry. Stem cell therapy in nervous system disorders is a growing field. The present research aimed to compare the effect of MSCs with that of estradiol benzoate or avosoya on the cerebellum of ovariectomized rats. Fifty eight adult female Wistar albino rats were classified into five groups. Control group (Group I) and four ovariectomized groups. Group II (ovariectomized rats received no treatment), Group III (injected subcutaneously with estradiol benzoate), Group IV (received avosoya orally) and Group V (treated with human umbilical cord blood derived mesenchymal stem cells [HUCBMSCs]). Cerebellar sections were stained with hematoxylin and eosin and cresyl fast violet. Immunoperoxidase reaction of glial fibrillary acidic protein (GFAP), estrogen receptor beta (Erβ) and Bax protein was also done. HUCBMSCs homing in rat cerebellum were detected by human albumin gene. Antioxidant enzyme levels were also measured in cerebellum homogenate. Decreased density of neurons in the three cortical layers with vacuolations and distorted Purkinje cells with pyknotic nuclei were observed in Group II. Group III cerebellar cortex showed normal architecture but some Purkinje cells had pyknotic nuclei. Group IV showed normal neuronal cells in the three cortical layers. Group V Purkinje cells were pyriform with vesicular nuclei, and basophilic cytoplasm. Small rounded cells with deeply stained nuclei appeared in the granular layer. In conclusion: estradiol benzoate and avosoya improve ovariectomy-induced cerebellar alteration, and MSCs show promising results in this field.

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Crossref · 10.4172/2157-7099.1000444

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  • FEN-induced oxidative stress increases mitochondrial membrane permeability, releasing cytochrome C into the cytosol, which activates caspase-9 and procaspase-3, triggering apoptosis.

    “This was in agreement with Ahmed et al. (2017) who referred this effect to increased mitochondrial membrane permeability caused by FEN-induced oxidative stress, which results in the release of cytochrome C into the cytosol. Apoptosis is triggered when cytochrome C activates caspase-9, which then cleaves and activates procaspase-3 (Soliman et al. 2017).”

    From Can coenzyme Q10 alleviate the toxic effect of fenofibrate on skeletal muscle? (2023) · cites this paper as Ahmed et al. 2017

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Authors
Ahmed, S. M., Abdelrahman, S. A., & Shalaby, S. M.
Venue
Journal of Cytology & Histology
Published
2017
Volume
08
Issue
01
ISSN
2157-7099 (ISSN-L)
OpenAlex
W2605813119
Cited by
7
References
61
Citations by year
2026: 1 · 2025: 1 · 2023: 1 · 2022: 3 · 2018: 1
FWCI
0.16
Type
journal article
Language
en
Open access
closed
Locations
Journal of Cytology & Histology (publishedVersion)
Topics
  • Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Menopause: Health Impacts and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
Keywords
mesenchymal stem cells, estradiol benzoate, ovariectomy, menopause, cerebellar cortex, human umbilical cord blood-derived mesenchymal stem cells, Purkinje cells, glial fibrillary acidic protein, estrogen receptor beta, Bax, antioxidant enzymes, neuroprotection, stem cell therapy

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