Go to:
Logótipo
Você está em: Start > Publications > View > Caspase-3 detection in human testicular spermatozoa from azoospermic and non-azoospermic patients
Map of Premises
Principal
Publication

Caspase-3 detection in human testicular spermatozoa from azoospermic and non-azoospermic patients

Title
Caspase-3 detection in human testicular spermatozoa from azoospermic and non-azoospermic patients
Type
Article in International Scientific Journal
Year
2011
Authors
Almeida C
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Cunha, M
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Ferraz, L
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Silva, J
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
barros, a
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Journal
Vol. 34
Pages: E407-E414
ISSN: 0105-6263
Publisher: Blackwell
Other information
Authenticus ID: P-002-M57
Abstract (EN): The apoptotic mechanisms underlying spermatogenesis in testis are poorly understood. In the present study, the rates of testicular spermatozoa with active caspase-3 were quantified in testicular samples with normal and impaired spermatogenesis. Testicular spermatozoa were collected from 18 men after testicular biopsy during assisted reproductive treatments: five presented oligozoospermia, four congenital bilateral absence of the vas deferens (CBAVD), five secondary obstructive azoospermia (sOAZ) and four hypospermatogenesis. Ejaculated samples were derived from six normozoospermic patients. Testicular spermatozoa were analysed using a fluorescence microscope and differences among groups were calculated using regression logistic models. Total rates of spermatozoa with active caspase-3 were significantly higher in sOAZ (78.6 +/- 13.9), followed by hypospermatogenesis (70.8 +/- 5.8), CBAVD (55.9 +/- 25.5), oligozoospermia (31.7 +/- 31.0) and normozoospermia (20.4 +/- 15.5). Distinct patterns of active caspase-3 were observed in testicular spermatozoa compartments: midpiece, equatorial region, acrosomal vesicle region, nucleus and cytoplasm. Hypospermatogenesis showed active caspase-3 mainly in the midpiece. In CBAVD, sOAZ and oligozoospermia, active caspase-3 was mainly in the nucleus, although no differences were found between oligozoospermia and hypospermatogenesis. In sOAZ, active caspase-3 in the spermatozoa nucleus was 1.89-fold higher than in CBAVD. Results suggest that tubular obstruction may induce nuclear lesions and that disrupted spermatozoa production observed in cases of hypospermatogenesis might be associated with mitochondrial lesions.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 8
Documents
We could not find any documents associated to the publication.
Related Publications

Of the same journal

Influence of 5a-dihydrotestosterone and 17 ss-estradiol on human Sertoli cells metabolism (2011)
Article in International Scientific Journal
Oliveira, PF; Alves, MG; Rato, L; Silva, J; Sa, R; barros, a; sousa, m; Carvalho, RA; cavaco, je; Socorro, S
Human mtDNA haplogroups and reduced male fertility: real association or hidden population substructuring (2005)
Article in International Scientific Journal
Pereira, L; Goncalves, J; Goios, A; Rocha, T; Amorim, A
Recommend this page Top
Copyright 1996-2025 © Faculdade de Medicina Dentária da Universidade do Porto  I Terms and Conditions  I Acessibility  I Index A-Z  I Guest Book
Page created on: 2025-07-07 at 06:20:25 | Acceptable Use Policy | Data Protection Policy | Complaint Portal