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1.
Genet Mol Res ; 14(2): 6583-90, 2015 Jun 12.
Article in English | MEDLINE | ID: mdl-26125865

ABSTRACT

The prevalence of Y chromosome microdeletions among azoospermic, severe oligozoospermic, moderate oligozoospermic, and mild oligozoospermic patients with varicocele-related and idiopathic infertility shows conflicting data in Asian countries. We aimed to detect this frequency in Northeast China, and investigated spermatogenic defects whether associated with varicocele or Y chromosome microdeletions. All samples underwent a thorough physical examination, semen analysis, and PCR analyses for Y chromosome microdeletions. We randomly selected 150 infertile non-obstructive azoospermic patients with left varicocele (Group 1), 150 idiopathic non-obstructive azoospermic infertility patients (Group 2), 150 infertile severe oligozoospermic patients with left varicocele (Group 3), 150 idiopathic severe oligozoospermic infertility patients (Group 4), 150 infertile moderate oligozoospermic patients with left varicocele (Group 5), 150 idiopathic moderate oligozoospermic infertility patients (Group 6), 150 infertile mild oligozoospermic patients with left varicocele (Group 7), 150 idiopathic mild oligozoospermic infertility patients (Group 8), and 60 healthy unrelated men with proven fertility were recruited as control subjects (Group 9). We observed that our samples from Northeastern China had a higher frequency of microdeletions among the non-obstructive azoospermic individuals with varicocele, as compared with other Asian countries. Furthermore, the spermatogenic defect is due to the underlying Y chromosome microdeletion, and not the varicocele itself. Although varicocele is not the cause of male infertility, it may be associated with male infertility in the Northeastern Chinese population.


Subject(s)
Chromosomes, Human, Y/genetics , Infertility, Male/genetics , Sex Chromosome Disorders of Sex Development/genetics , Varicocele/genetics , Adult , Azoospermia/genetics , Azoospermia/pathology , China , Chromosome Deletion , Humans , Infertility, Male/pathology , Male , Middle Aged , Oligospermia/genetics , Oligospermia/pathology , Sex Chromosome Aberrations , Sex Chromosome Disorders of Sex Development/pathology , Spermatogenesis/genetics , Varicocele/complications , Varicocele/pathology
2.
Andrologia ; 46(5): 535-40, 2014 Jun.
Article in English | MEDLINE | ID: mdl-23701642

ABSTRACT

Azoospermia factor (AZF) microdeletions are the most frequent genetic cause of male infertility after Klinefelter's syndrome. Although some assisted reproductive techniques such as intracytoplasmic sperm injection (ICSI) have been successfully introduced to clinical treatment for infertile males, the AZF microdeletions might be transmitted from infertile fathers to their male offspring during these procedures. Thus, it is important to carefully evaluate AZF microdeletions in infertile males before assisted reproductive techniques are performed. In this article, we aimed to investigate the frequencies of AZF microdeletions in 137 infertile males with azoospermia and severe oligozoospermia from Jilin province of China and analyse the relationship between the levels of reproductive hormones and AZF microdeletions. Result analysis showed that AZF microdeletions were present in 8 (8.70%) azoospermic males and 3 (6.67%) severely oligozoospermic males. The most frequent microdeletions were detected in the AZFc region, followed by AZFb + c, AZFb and AZFa. And there was no significant correlation between the AZF microdeletion and the levels of reproductive hormones. These findings reinforce the necessity of AZF microdeletion testing among infertile males prior to employment of assisted reproduction techniques in Jilin province of China.


Subject(s)
Azoospermia/genetics , Sequence Deletion , Base Sequence , China , DNA Primers , Gonadal Steroid Hormones/blood , Humans , Male , Polymerase Chain Reaction
3.
J Int Med Res ; 40(3): 1182-91, 2012.
Article in English | MEDLINE | ID: mdl-22906293

ABSTRACT

OBJECTIVE: To determine characteristics of classical and partial deletions of the Y chromosome azoospermia factor (AZF) region transmitted from father to son by natural fertilization. METHODS: Patients from northeastern China with primary male infertility (n = 10) and their fathers were investigated. Healthy fertile men and women were recruited as positive and negative controls, respectively. The Y chromosome microdeletions were detected by polymerase chain reaction. Serum concentrations of reproductive hormones were determined by electrochemiluminescence immunoassay and enzyme-linked immunosorbent assay. RESULTS: Expansions of microdeletions were observed in seven father­son pairs; de novo microdeletions were found in the remaining three father­son pairs. The Y chromosome microdeletions were larger in sons than in their fathers. Patients with infertility had significantly higher levels of follicle stimulating hormone and lower levels of inhibin B than fertile men. CONCLUSIONS: The Y chromosome microdeletions were transmitted from father to son via natural transmission. These microdeletions may expand during transmission or arise de novo, possibly resulting in reduced fertility.


Subject(s)
Chromosome Deletion , Chromosomes, Human, Y , Gene Transfer Techniques , Adult , Base Sequence , Case-Control Studies , China , DNA Primers , Enzyme-Linked Immunosorbent Assay , Female , Hormones/blood , Humans , Infertility, Male/genetics , Karyotyping , Male , Polymerase Chain Reaction
4.
Genet Mol Res ; 11(3): 2422-31, 2012 Aug 16.
Article in English | MEDLINE | ID: mdl-22614455

ABSTRACT

We investigated the frequency and types of Y-chromosome microdeletions and chromosomal anomalies in non-obstructive azoospermic and severely oligozoospermic infertile males in northeastern China. The sample consisted of 519 infertile males (456 azoospermic, 63 severely oligozoospermic). PCR assays for Y-chromosome microdeletions and chromosome analysis were performed on all patients and controls. Array-comparative genomic hybridization was performed for three patients with chromosomal anomalies. Fifty-nine of 519 patients (11.37%) had Y-chromosome microdeletions. Microdeletions were found in 11.18% (51/456) of the non-obstructive azoospermic patients and in 12.7% (8/63) of the severely oligozoospermic patients. Eleven of 51 non-obstructive azoospermic patients with Y-chromosome microdeletions had multiple segmental deletions in the AZFb+c regions; four of these patients had chromosomal anomalies. Our sample from northeastern China had a higher frequency of microdeletions among severely oligozoospermic than among non-obstructive azoospermic males.


Subject(s)
Azoospermia/genetics , Chromosome Deletion , Chromosomes, Human, Y/genetics , Adult , China , Comparative Genomic Hybridization , Humans , Infertility, Male , Karyotyping , Male , Middle Aged , Sequence Tagged Sites , Sex Chromosome Aberrations , Sex Chromosome Disorders of Sex Development/genetics , Young Adult
5.
Neuroscience ; 209: 1-11, 2012 May 03.
Article in English | MEDLINE | ID: mdl-22402346

ABSTRACT

In our previous study, we found that the sonic hedgehog (Shh) signaling pathway is activated in neurons under oxidative stress and plays a neuro-protective role [Dai RL, et al. (2011) Neurochem Res 36:67-75]; we are led to postulate that the Shh might be released by astrocytes, thereby protecting neurons against oxidant injury. In primary cultured astrocytes of rats, we found that treatment with 100 µM H2O2 for 24 h induced a significant increase in the mRNA and protein levels of Shh, Patched1, and Gli-1, and the increase was substantially greater in astrocytes than in neurons. In the coculture systems of astrocytes and neurons under the H2O2 treatment, blocking the Shh signaling pathway with 5E1 (an antibody against the N-terminal domain of Shh) could block the neuroprotective activity of astrocytes on cocultured neurons. In this study, we found that treatment with H2O2 (100-800 µM) for 24 h caused cell death of astrocytes in a concentration-dependent manner. MTT reduction and Trypan Blue exclusion assay showed that exogenous Shh increased survival rate of the H2O2-treated astrocytes, whereas pretreatment with cyclopamine (a specific inhibitor of the Shh signaling pathway) or 5E1 decreased the survival rate of the H2O2-treated astrocytes. Shh also inhibited H2O2-induced apoptosis of astrocytes, and this effect could be partially reversed by cyclopamine. We also found that Shh promoted the phosphorylation of AKT, but had no significant effect on p38 or extracellular signal regulated kinases 1 and 2 (ERK 1/2) in H2O2-treated astrocytes. Blocking Shh or phosphoinositide 3-kinases (PI3-K)/AKT signaling pathway with cyclopamine or LY294002 decreased the survival rate of astrocytes, induced cell apoptosis, upregulated the expression of Bax, and downregulated the expression of Bcl-2. We are led to conclude that the oxidative stress induces astrocytes to secrete endogenous Shh and exogenous administration of Shh might protect the astrocytes from oxidative stress by activating PI3-K/AKT/Bcl-2 pathway.


Subject(s)
Astrocytes/metabolism , Hedgehog Proteins/metabolism , Oxidative Stress/physiology , Signal Transduction/physiology , Animals , Apoptosis/drug effects , Apoptosis/physiology , Astrocytes/drug effects , Cells, Cultured , Coculture Techniques , Enzyme-Linked Immunosorbent Assay , Fluorescent Antibody Technique , Hydrogen Peroxide/pharmacology , Immunoblotting , Neurons/drug effects , Neurons/metabolism , Oxidants/pharmacology , Oxidative Stress/drug effects , Phosphatidylinositol 3-Kinases/metabolism , Proto-Oncogene Proteins c-akt/metabolism , Proto-Oncogene Proteins c-bcl-2/metabolism , Rats , Rats, Sprague-Dawley , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , Signal Transduction/drug effects
6.
J Int Med Res ; 39(1): 33-40, 2011.
Article in English | MEDLINE | ID: mdl-21672305

ABSTRACT

This study investigated the effects of Ureaplasma urealyticum infection and raised seminal leucocyte levels on sperm morphology in 967 infertile males and 201 fertile healthy volunteers. U. urealyticum infection led to a significant decrease in the percentage of morphologically normal sperm in infertile males. There was a clear correlation between U. urealyticum infection, raised seminal leucocytes and abnormal sperm morphology. The percentage of morphologically normal sperm was significantly lower in U. urealyticum-positive than U. urealyticum-negative infertile males or fertile controls. The percentage of morphologically normal sperm was lowest in U. urealyticum-positive males with raised seminal leucocytes. Previous studies have found raised seminal leucocyte levels to be associated with reactive oxygen species. The authors suggest that oxidative stress contributes to the effects of U. urealyticum on sperm morphology. In conclusion, U. urealyticum infection can negatively affect sperm morphology and this study provided two possible mechanistic explanations.


Subject(s)
Infertility, Male/microbiology , Infertility, Male/physiopathology , Semen/cytology , Spermatozoa/cytology , Ureaplasma Infections/microbiology , Ureaplasma Infections/physiopathology , Adult , Case-Control Studies , China , Humans , Infertility, Male/pathology , Leukocyte Count , Leukocytes/cytology , Longitudinal Studies , Male , Oxidative Stress , Reactive Oxygen Species/metabolism , Semen/microbiology , Semen Analysis , Sperm Motility , Spermatozoa/microbiology , Ureaplasma Infections/pathology , Ureaplasma urealyticum/physiology
7.
Shi Yan Sheng Wu Xue Bao ; 34(2): 127-30, 2001 Jun.
Article in Chinese | MEDLINE | ID: mdl-12549105

ABSTRACT

We used callus of medical plant, Ningxia Lycium barbarum. L as material to induce somatic embryo genesis, and used multitracer technique and gamma-ray energy spectrum analytical method to study different concentration of AgNO3 on some absorption of trace metal ions during the somatic embryogenesis of Lycium barbarum. L. The results show that (1) when the concentration of AgNO3 is less then 50 mg/L, with the increase of AgNO3 concentration, the absorption rate of some metal ions is increasing, but when the concentration is excess of such concentration, the effects on the absorption rate are different. Ag+ has the effect of coordination, resistance or competition on the absorption of metal ions. (2) AgNO3 in suitable concentration will promote cell differentiation and somatic embryogenesis. When the concentration of AgNO3 is less then 50 mg/L, along with the increase of the concentration, the frequency of somatic embryogenesis is increased, and Ag+ has the promotion on the somatic embryogenesis of Lycium barbarum. L. While the concentration is up to 50 mg/L, it will mostly raise somatic embryogenesis in calli, the amount of callus is about 3 times as much as that of contrast group (in which AgNO3 is not added). When excess of this concentration point, Ag+ has toxic effect, and the somatic embryogenesis is inhibited remarkably.


Subject(s)
Lycium/growth & development , Silver Nitrate/pharmacology , Trace Elements/metabolism , Absorption , Culture Techniques , Dose-Response Relationship, Drug , Lycium/metabolism
8.
Shi Yan Sheng Wu Xue Bao ; 32(3): 297-300, 1999 Sep.
Article in Chinese | MEDLINE | ID: mdl-12548812

ABSTRACT

The protein and DNA content in somatic embryos of Lycium barbarum L were analysed using quantitative stereologicai procedure formed from Cell Morphometry. The photos were transformed into digital images by the Sharp JX-610 scanner. Then the quantity of protein and DNA was count applying digital images processing software. By the result we discuss the relationship between changes in protein and DNA metabolize dynamic and somatic embryogensis.


Subject(s)
DNA, Plant/metabolism , Lycium/growth & development , Plant Proteins/metabolism , Culture Techniques , Lycium/metabolism , Plant Leaves/growth & development , Plant Leaves/metabolism
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