Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7635
Title: Expression of vascular endothelial growth factor and transforming growth factor alpha in rat testis during chronic renal failure
Authors: Seval-Celik, Y.
Akkoyunlu, G.
Kocamaz, Erdoğan
Köksal, I.T.
Özer, S.
Baykara, M.
Demir, R.
Keywords: Chronic renal failure
IHC
Peritoneal dialysis
Rat
Spermatogenesis
Testis
TGF-?
VEGF
paraffin
transforming growth factor alpha
vasculotropin
vasculotropin A
adult
animal cell
animal experiment
animal model
animal tissue
Article
cell nucleus
chronic kidney failure
controlled study
cytoplasm
immunohistochemistry
male
meiosis
microscopy
morphology
nonhuman
partial nephrectomy
peritoneal dialysis
protein expression
protein localization
rat
seminiferous tubule epithelium
spermatid
spermatocyte
spermatogenesis
spermatogonium
testis
animal
disease model
gene expression regulation
genetics
human
metabolism
pathophysiology
Wistar rat
Animalia
Rattus
Animals
Disease Models, Animal
Gene Expression Regulation
Humans
Immunohistochemistry
Kidney Failure, Chronic
Male
Rats
Rats, Wistar
Vascular Endothelial Growth Factor A
Publisher: Via Medica
Abstract: Introduction: Vascular endothelial growth factor (VEGF) is known to influence testis function. Transforming growth factor alpha (TGF-?) is expressed in the postnatal testis, and has been demonstrated to stimulate testis development. Systemic diseases such as chronic renal failure (CRF) interfere with hypothalamic-pituitary-go­nadal axis, which may cause defective steroidogenesis and gonadal functions. The aim of this study was to inve­stigate the expression and localization of VEGF and TGF-? in testicular tissues of experimental CRF model.
Material and methods: Experimental CRF was induced in rats by the resection of more than 85% of renal mass. The expression of VEGF and TGF-? in testicular tissues were assessed by immunohistochemistry on paraffin sections of control, CRF-nondialysed and CRF-dialysed rats.
Results: The microscopic evaluation of the testicular structure showed that CRF did not affect testicular histology. Immunohistochemical evaluation showed that VEGF was expressed in the cytoplasm of primary and secondary spermatocyte series as well as the early spermatids. Staining intensity was lower in sperma­tocytes going through the first meiotic division. TGF-? was expressed in the nuclei of spermatogonia and primary spermatocytes with stronger staining intensity in spermatogonia. The intensity of VEGF staining was similar in control and experimental animals, however, TGF-? expression was lower in the CRF group.
Conclusions: The continuous expression of VEGF in spermatocytes and spermatids suggests that the applied model of CRF does not directly disrupt morphology of seminiferous epithelium, thus also spermiogenesis. However, difference between control rats and CRF group in TGF-? immunopositivity, which was localised in spermatogonial mitosis step, may suggest the interference of CRF with early stages of spermatogenesis. © Polish Society for Histochemistry and Cytochemistry.
URI: https://hdl.handle.net/11499/7635
https://doi.org/10.5603/FHC.a2014.0032
ISSN: 0239-8508
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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