“…Unilateral cryptorchidism in animals occurs significantly more often than bilateral cryptorchidism (1). The left cryptorchid testis in dogs is usually located in the abdominal cavity, while the right cryptorchid testis can be found in the inguinal canal (1). The cases of cryptorchidism in European bison recorded in our study deviated from this rule, since both left and right cryptorchid testes were found in the inguinal canal.…”
Section: Resultscontrasting
confidence: 66%
“…The normal development of the gubernaculum is Cryptorchidism can be unilateral or bilateral (30). Unilateral cryptorchidism in animals occurs significantly more often than bilateral cryptorchidism (1). The left cryptorchid testis in dogs is usually located in the abdominal cavity, while the right cryptorchid testis can be found in the inguinal canal (1).…”
SummaryThe aim of this study was to find whether the coefficient of inbreeding is correlated with the incidence of cryptorchidism in the Białowieża line of bison.Our In 461 male European bison older than 1 year, there were 18 cases of cryptorchidism. In the animals born in the first decade, two autopsical cases of cryptorchidism (0.045%) were recorded, and 4 cases of cryptorchidism (0.03%) were found in the animals from the second decade. Among the bison born in the third decade, there were no cases of cryptorchidism. In the fourth decade, 7 cases of cryptorchidism (0.071%) were diagnosed, and among the bison born during the fifth decade, there were 5 cases (0.111%).The Pearson correlation coefficient suggests that, as the value of the coefficient of inbreeding rises, there is an increase in cryptorchidism cases in male European bison.
“…Unilateral cryptorchidism in animals occurs significantly more often than bilateral cryptorchidism (1). The left cryptorchid testis in dogs is usually located in the abdominal cavity, while the right cryptorchid testis can be found in the inguinal canal (1). The cases of cryptorchidism in European bison recorded in our study deviated from this rule, since both left and right cryptorchid testes were found in the inguinal canal.…”
Section: Resultscontrasting
confidence: 66%
“…The normal development of the gubernaculum is Cryptorchidism can be unilateral or bilateral (30). Unilateral cryptorchidism in animals occurs significantly more often than bilateral cryptorchidism (1). The left cryptorchid testis in dogs is usually located in the abdominal cavity, while the right cryptorchid testis can be found in the inguinal canal (1).…”
SummaryThe aim of this study was to find whether the coefficient of inbreeding is correlated with the incidence of cryptorchidism in the Białowieża line of bison.Our In 461 male European bison older than 1 year, there were 18 cases of cryptorchidism. In the animals born in the first decade, two autopsical cases of cryptorchidism (0.045%) were recorded, and 4 cases of cryptorchidism (0.03%) were found in the animals from the second decade. Among the bison born in the third decade, there were no cases of cryptorchidism. In the fourth decade, 7 cases of cryptorchidism (0.071%) were diagnosed, and among the bison born during the fifth decade, there were 5 cases (0.111%).The Pearson correlation coefficient suggests that, as the value of the coefficient of inbreeding rises, there is an increase in cryptorchidism cases in male European bison.
“…Understanding the effects of retention on testicular development is thus crucial when attempting to give evidence-based advice about whether a testicle that finally descends into the scrotum in a 2-to 3-year-old colt still has the capacity to develop into a grossly normal testicle. This explains the value of the report by Almeida et al [1] that the retained testicles from 2-to 3-year-old cryptorchids maintain the molecular characteristics of prepubertal testes. This suggests that retention leads to a delay in development without, at least during the first 3 years, loss of the potential to develop spermatogenetic capacity if and when relocated to a suitable environment, i.e.…”
mentioning
confidence: 72%
“…This explains the value of the report by Almeida et al . that the retained testicles from 2‐ to 3‐year‐old cryptorchids maintain the molecular characteristics of prepubertal testes. This suggests that retention leads to a delay in development without, at least during the first 3 years, loss of the potential to develop spermatogenetic capacity if and when relocated to a suitable environment, i.e.…”
mentioning
confidence: 93%
“…In short, the study by Almeida et al . is a useful addition to the literature on the effects of cryptorchidism on testicular development and maturation, but also a useful reminder that there is still a lot of research to be done to establish how large a role heritable genetic mutations play in equine cryptorchidism and how widespread any genetic predisposition(s) currently is, in order to determine whether cryptorchidism‐associated genetic mutations differ between horse breeds and/or phenotypic forms of cryptorchidism, and to determine whether there are any firm grounds for promoting phenotypic selection against cryptorchidism or whether selection should instead be based on genetic testing; any proposal should be supported by a prediction of how successful attempts to select against cryptorchidism are likely to be. Although there are therefore considerable challenges to be met, the sequencing of the equine genome and subsequent development of techniques for genome‐wide gene mutation screening means that these hurdles are considerably less daunting than they were a decade ago.…”
Testicular ischemia reperfusion injury (tIRI) is considered as the underlying mechanism of testicular torsion, which can cause male infertility. tIRI-induced damage was investigated by assessing the gene expression of spermatogenesis master transcription factors (TFs) and that of major adhesion molecules of the blood-testis barrier. The effect of lutein, a hydroxyl carotenoid, in alleviating tIRI-induced damage was also studied. Male Sprague-Dawley rats were divided into three groups: sham, unilateral tIRI, and tIRI + lutein (0.2 mg/kg). tIRI was induced by occlusion of the testicular artery for 1 h, followed by 4 h of reperfusion. Lutein was injected 15 min after the start of ischemia. Histological analysis and real-time polymerase chain reaction revealed significant decreases in tissue biopsy scores, reduced seminiferous tubule diameters, and downregulated the mRNA expression of the TFs cAMP-responsive element modulator (CREM), TATA box-binding protein-related factor 2 (TRF2), and regulatory factor X 2 (RFX2) compared with the sham group. Lutein treatment reversed these effects. The mRNA expression of the adhesion molecules N-cadherin, nectin-2, claudin-11, occludin, and connexin-43 was significantly downregulated during tIRI, but this change was prevented by lutein treatment. In addition, lutein normalized the tIRI-induced increase in total antioxidant capacity, increased malondialdehyde (MDA) levels, augmented number of TdT-mediated dUTP-X nick-end labeling (TUNEL)-positive nuclei, and activated caspase-8 pathway. The components of survivor activating factor enhancement (SAFE) were also activated during tIRI. Increased tissue expression of TNF-α and its receptor, TNFR1, was accompanied by increased phosphorylation of Janus kinase (JAK) and STAT3, which was prevented by lutein treatment. Our findings suggested that tIRI-induced spermatogenic damage may involve modulation of the SAFE pathway and could benefit from lutein treatment.
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