Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 28
Filter
1.
Chinese Journal of School Health ; (12): 475-478, 2024.
Article in Chinese | WPRIM | ID: wpr-1016753

ABSTRACT

Objective@#To explore the association between bedroom light at night (LAN) exposure and body mass index (BMI) in children at 1 year follow up, so as to provide new strategies for obesity prevention.@*Methods@#From December 2021 to May 2022, cluster random sampling was conducted, involving 648 children from two primary schools in Tianchang, Chuzhou City, Anhui Province, China, to assess bedroom LAN exposure of children during sleep. A questionnaire survey and physical examination were carried out in May 2022. Multivariate linear regression was performed to analyze the correlation between bedroom LAN exposure and BMI variable quantity at 1 year follow up (May, 2023).@*Results@#The median intensity of bedroom LAN exposure during the sleep episode was [1.11(0.35,3.24)lx] in children. The proportion of the sample exposed to an average light intensity of ≥3 lx was 27.5%, while 19.0% was exposed to a LAN intensity of ≥5 lx during the sleep episode. In the multivariable linear regression, after adjusting for covariates, including sex, baseline age, sleep duration, family monthly income, and maternal education level, exposure to a 1 h-average post bedtime LAN intensity of ≥3 lx ( β=0.25, 95%CI =0.05-0.44) and LAN≥5 lx ( β=0.34, 95% CI = 0.12-0.55) was associated with a gain of 0.25 and 0.34 kg/m 2, respectively, in the children s BMI at the 1 year follow up ( P < 0.05).@*Conclusions@#A positive correlation was found between bedroom LAN exposure and BMI variable quantity at 1 year follow up in children. Thus, reduced bedroom LAN exposure might be useful for interventions aimed at obesity prevention.

2.
Chinese Journal of Stomatology ; (12): 455-461, 2022.
Article in Chinese | WPRIM | ID: wpr-935887

ABSTRACT

Today, there is greater awareness on the association between oral diseases and respiration diseases after the outbreak of COVID-19. However, confusion regarding the oral health management and medical risk prevention for patients with chronic airway diseases has been remained among dental clinicians. Therefore, the dental experts of the Fifth General Dentistry Special Committee, Chinese Stomatological Association, combined with the experts of respiratory and critical care medicine, undertook the formation of consensus on the oral health management of patients with chronic airway diseases in order to help dental clinicians to evaluate medical risks and make better treatment decision in clinical practice. In the present consensus report, the relationship of oral diseases and chronic airway diseases, the oral health management and the treatment recommendations of patients with chronic airway diseases are provided.


Subject(s)
Humans , COVID-19 , Consensus , Oral Health , Oral Medicine
3.
Chinese Journal of Stomatology ; (12): 462-473, 2022.
Article in Chinese | WPRIM | ID: wpr-935888

ABSTRACT

With the aging process of population in the society, the prevalence of cardiovascular diseases (CVD) in China is increasing continuously and the number of dental patients with CVD is increasing gradually too. Due to the lack of guidelines for dental patients with CVD in our country, how to implement standardized preoperative evaluation and perioperative risk prevention remains a problem to be solved for dentists at present. The present expert consensus was reached by combining the clinical experiences of the expert group of the Fifth General Dentistry Special Committee, Chinese Stomatological Association and respiratory and cardiology experts in diagnosis and treatment for CVD patients, and by systematically summarizing the relevant international guidelines and literature regarding the relationship between CVD and oral diseases and the diagnosis and treatment of dental patients with heart failure, hypertension and antithrombotic therapy. The consensus aims to provide, for the dental clinicians, the criteria on diagnosis and treatment of CVD in dental patients in China so as to reduce the risk and complications, and finally to improve the treatment levels of dental patients with CVD in China.


Subject(s)
Humans , Cardiovascular Diseases/prevention & control , China/epidemiology , Consensus , Dental Care , Oral Medicine
4.
Chinese Journal of Stomatology ; (12): 523-528, 2022.
Article in Chinese | WPRIM | ID: wpr-935896

ABSTRACT

Emerging evidence suggests that, along with dietary, genetic and environmental factors, gut microbiota plays a role in the progress of colorectal cancer. Dysbiosis of oral flora in patients with periodontitis affects the composition of microbial community in the gut, impairs gut barrier function, and induces a proinflammatory microenvironment, all of which contribute to the progression of colorectal cancer. In view of the influences by microbiota dysbiosis, this article reviews the role of periodontitis in affecting the occurrence and development of colorectal cancer.


Subject(s)
Humans , Colorectal Neoplasms , Dysbiosis/complications , Gastrointestinal Microbiome , Microbiota , Periodontitis/complications , Tumor Microenvironment
5.
Article in Chinese | WPRIM | ID: wpr-792833

ABSTRACT

Objective@#To explore the clinical manifestations, histopathological features, diagnosis, treatment and prognosis of Rosai-Dorfman′s disease (RDD) in the maxillofacial region and to review the relevant literature in order to improve the understanding, diagnosis and treatment of oral and maxillofacial RDD.@*Methods @#The clinical manifestations, histopathological features, diagnosis, treatment, and prognosis of a patient with RDD in the maxillofacial region admitted to Shenzhen People′s Hospital were analyzed, and the literature was reviewed for analysis. @*Results@#The clinical manifestations were palpable masses of 3.5 cm × 2.0 cm × 1.0 cm in the right cheek and 3.0 cm × 2.0 cm × 1.0 cm in the right submaxillary area, with clear boundaries, good mobility, medium and hard textures, respectively, no tenderness, smooth surfaces, and no obvious nodules. On contrast-enhanced and plain CT scans of the maxilla and neck, a diffuse soft tissue shadow was seen in the right maxillofacial region with an unclear boundary and uniform density, and the contrast-enhanced scan also showed moderate and uniform enhancement. The primary diagnosis was right maxillofacial lesions. The tumor was resected surgically. The pathological report was right buccal and right submaxillary extranodal RDD. Under light microscopy, nodular lesions in the fibrous fat tissue were found, which were composed of light and deep staining areas. The light staining areas consisted of patchy, polygonal cells with large volumes and rich cytoplasm, in which lymphocytes and neutrophils could be seen stretching into the movement; the deep staining areas were composed of lymphocytes and plasma cells. IHC: S-100 (+), CD68 (+), CD163 (+), CD1a (-), CD21FDC (+), langerin (-), IgG (+), IgG4 (+). No recurrence was found 11 months after the operation. RDD is a rare, benign and self-limited tissue and cell disease and consists of multiple lesions in the maxillofacial region. Its imaging features are similar to those of lymphoma. Its pathological features are large volumes, rich cytoplasm and phagocytosis of lymphocytes and plasma cells. Generally, RDD only needs to be observed, and individuals with symptoms or the involvement of important organs need to be treated; the first choice for the extranodal type is drug treatment, with radiotherapy administered if the central nervous system is involved. Surgery is recommended if involvement of important organs and compression of the trachea are observed; chemotherapy should be used for diffuse RDD. Most patients with RDD experienced relapse or remission of the disease; a few patients died because of the involvement of important organs or complications.@*Conclusion @#The clinical manifestations of maxillofacial RDD vary and lack specific imaging features, and pathological immunohistochemistry is the gold standard for diagnosis. The etiology is not completely clear, the treatment methods are varied, and the prognosis is related to the involved range of the disease.

6.
Article in English | WPRIM | ID: wpr-310915

ABSTRACT

<p><b>OBJECTIVE</b>To determine the effects of Ginkgo biloba extract (EGB) on major periodontal pathogens in subgingival plaque.</p><p><b>METHODS</b>Sixty patients with moderate to severe periodontitis were selected and randomly assigned to 3 groups: EGB group, a positive (periocline) and a negative control groups. Subgingival plaque samples were collected before treatment and 1 week, 2 months and 4 months after treatment. The detection rates of 4 major periodontal pathogens-Treponema denticola (Td), Tannerella forsythus (Tf), Prevotella intermedia (Pi), and Porphyromonas gingivalis (Pg)-were detected by polymerase chain reaction (PCR). Clinical indicators were examined before treatment, 3 and 6 months after treatment.</p><p><b>RESULTS</b>EGB significantly decreased the detection rate of all the 4 pathogens 1 week after treatment, and then gradually increased at 2 and 4 months. EGB's inhibition effect was better than or comparable to periocline, except for Pg in short-term. The difference of plaque index (PLI) and bleeding index (BI) was not statistically significant among the groups, while for probing depth (PD) and attachment loss (AL), the difference was statistically significant between the EGB group and negative control group at 3 and 6 months after treatment.</p><p><b>CONCLUSION</b>EGB significantly inhibited major periodontal pathogens and can be used as an adjuvant for periodontitis treatment.</p>


Subject(s)
Humans , Adjuvants, Pharmaceutic , Pharmacology , Therapeutic Uses , Bacteria , Dental Plaque , Drug Therapy , Microbiology , Follow-Up Studies , Ginkgo biloba , Chemistry , Periodontium , Microbiology , Pathology , Plant Extracts , Pharmacology , Therapeutic Uses , Polymerase Chain Reaction , Treatment Outcome
7.
National Journal of Andrology ; (12): 799-804, 2011.
Article in Chinese | WPRIM | ID: wpr-305787

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the role of dynactin 1 (Dctn1) in the process of mouse spermiogenesis.</p><p><b>METHODS</b>Western blot and indirect immunofluorescence were used to analyze the expression and location of Dctn1 in the mouse testis and spermatozoa. The highest efficiency of small interference RNA (siRNA) was verified by GC2-spd cell line in vitro and in vivo studies, respectively. Dctn1 siRNA mixed with the indicator (0.4% trypan blue) was injected into the seminiferous tubules of 3-week-old ICR mice through rete testis microinjection, and negative control siRNA injected into the control testes. The normal group included 3-week-old ICR mice that did not receive any treatment. Spermatozoa were collected from the cauda epididymis 3 weeks after siRNA injection for morphological analysis.</p><p><b>RESULTS</b>Dctn1 was mainly localized in the tail of spermatozoa. After interference, the sperm tail abnormality in the Dctn1 siRNA group was (23.57 +/- 0.55)%, significantly higher than (12.35 +/- 2.29)% in the control (P < 0.01, n = 3), and it was (3.37 +/- 0.69)% in the normal group.</p><p><b>CONCLUSION</b>Dctn1 plays an important role in mouse spermiogenesis, and mainly affects the formation of the tail of spermatozoa.</p>


Subject(s)
Animals , Male , Mice , Dynactin Complex , Mice, Inbred ICR , Microinjections , Microtubule-Associated Proteins , Genetics , Metabolism , RNA, Small Interfering , Rete Testis , Metabolism , Seminiferous Tubules , Metabolism , Sperm Count , Sperm Motility , Spermatogenesis , Spermatozoa , Metabolism , Testis , Metabolism
8.
National Journal of Andrology ; (12): 516-522, 2011.
Article in Chinese | WPRIM | ID: wpr-305853

ABSTRACT

<p><b>OBJECTIVE</b>To study the expression of Annexin A7 in the mouse testis, especially in different types of spermatogonia.</p><p><b>METHODS</b>We prepared Annexin A7 recombinant protein using prokaryotic expression, adsorbed the Annexin A7 antibody with it after identified by mass spectrometry, and detected the expression of Annexin A7 by Western-blot and immunohistochemistry.</p><p><b>RESULTS</b>Annexin A7 was expressed in a development-dependent manner in the spermatogonia of the prepubertal mice and in the type-A single (As) and type-A paired (Apr) spermatogonia of adult mice. These results were confirmed by the co-localization of Annexin A7 and Stra8, a known determinant of differentiated spermatogonial stem cells (SSCs).</p><p><b>CONCLUSION</b>Annexin A7 is the internal factor of As and Apr spermatogonia, which might be involved in the biological functions of SSCs.</p>


Subject(s)
Animals , Male , Mice , Annexin A7 , Metabolism , Spermatogonia , Cell Biology , Metabolism , Stem Cells , Cell Biology , Metabolism
9.
National Journal of Andrology ; (12): 345-348, 2010.
Article in Chinese | WPRIM | ID: wpr-295061

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the phenotype, pathogenesis and molecular biological features of 46, XX testicular disorder of sex development.</p><p><b>METHODS</b>We obtained the history of 2 patients with 46, XX testicular disorder of sex development, examined the cavitas pelvis by type-B ultrasonography, analyzed the karyotype of the chromosome, and detected the genes SRY, YRRM1, DYS240 and DAZ by PCR amplification.</p><p><b>RESULTS</b>Microrchidia, azoospermia and maldevelopment of secondary sex characteristics were observed in both of the patients, but ultrasonography revealed no female internal genitals. Their chromosome gender was karyotyped as 46, XX, with the SRY gene positive in both, but the YRRM1 gene positive in only one of the cases.</p><p><b>CONCLUSION</b>Chromosome karyotyping and detection of the SRY gene for patients with abnormal sex development can give us an insight into the genetic pathogenesis and provide us with scientific evidence for the diagnosis and treatment of the condition.</p>


Subject(s)
Adult , Humans , Male , Genes, sry , Gonadal Dysgenesis, 46,XX , Genetics , Nuclear Proteins , Genetics , RNA-Binding Proteins , Genetics
10.
Chinese Journal of Stomatology ; (12): 668-672, 2010.
Article in Chinese | WPRIM | ID: wpr-243086

ABSTRACT

<p><b>OBJECTIVE</b>To establish a model of chronic periodontitis (CP) accompanied with chronic obstructive pulmonary disease (COPD) in SD rats and investigate the relationship between chronic periodontitis and COPD.</p><p><b>METHODS</b>Equal gender SD rats were randomly divided into 4 groups, A: control group, B: CP group, C: COPD group, D: COPD with CP group (n = 10, respectively). Each group was subjected to its predesigned intervention to establish a specific disease model. After 10 weeks, animals were sacrificed. The level of alveolar bone loss, lung function measurement, and the histopathological changes of periodontal and lung tissues were examined. The serum tumor necrosis factor (TNF)-α level was detected by enzyme-linked immunoabsorbent assay kits.</p><p><b>RESULTS</b>Bleeding index (BI) levels of group A and C were (0.25 ± 0.04) and (1.30 ± 0.25), respectively. Attachment loss was (0.43 ± 0.02) and (0.51 ± 0.02) mm. BI levels in group B and D were significantly higher than those in group A and C. Forced expiratory volume in 0.2 second to forced vital capital ratio (FEV(0.2)/FVC) values in group B, C and D were significantly lower than that in group A. Pulmonary function were worse in group D than that in group C (P < 0.05). The levels of serum TNF-α, a sensitive indicator of both diseases, were increased in all test groups compared with the control, and increased most in group D.</p><p><b>CONCLUSIONS</b>The chronic periodontitis and chronic obstructive pulmonary disease model was established in SD rat. The chronic periodontitis may be a risk factor for promoting and inducing COPD.</p>


Subject(s)
Animals , Rats , Alveolar Bone Loss , Chronic Periodontitis , Disease Models, Animal , Forced Expiratory Volume , Lung , Pulmonary Disease, Chronic Obstructive , Tumor Necrosis Factor-alpha
11.
National Journal of Andrology ; (12): 911-914, 2010.
Article in Chinese | WPRIM | ID: wpr-266246

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expression of carbonic anhydrase II (CA2) in human testes and spermatozoa, and to compare the expressions of CA2 in ejaculated spermatozoa between normozoospermic and asthenozoospermic men.</p><p><b>METHODS</b>The localization of CA2 in human testes was observed by immunohistochemistry, and that in human sperm by immunofluorescence. Western blot was used to detect the expression of CA2 in the semen samples obtained from 16 normozoospermic and 16 asthenozoospermic volunteers.</p><p><b>RESULTS</b>The CA2 protein was shown to be localized in the tail of elongating spermatids by immunohistochemistry and in the flagellum of human sperm by immunofluorescence. Western blot revealed an obviously increased expression of CA2 in the spermatozoa of asthenozoospermic patients, with statistically significant difference from the normozoospermic group (1.84 +/- 0.32 vs 1.41 +/- 0.26, P < 0.05).</p><p><b>CONCLUSION</b>The CA2 protein is expressed in the spermatogenic stage of elongating spermatids in human testes and localized in the sperm tail. The expression of CA2 is significantly increased in the spermatozoa of asthenozoospermic men, which might be responsible for low sperm motility.</p>


Subject(s)
Humans , Male , Asthenozoospermia , Metabolism , Carbonic Anhydrase II , Metabolism , Sperm Motility , Spermatozoa , Metabolism , Testis , Metabolism
12.
Asian Journal of Andrology ; (6): 229-239, 2009.
Article in English | WPRIM | ID: wpr-284679

ABSTRACT

Prior to fertilization sperm has to undergo an activation process known as capaciation, leading to the acrosome reaction. Till now, little is known about the mechanism for preventing premature capacitation in sperm although decapacitation factors from various sources have been thought to be involved. In this study, we report that NYD-SP27, an isoform of phospholipase C Zeta 1 (PLCZ1), is localized to the sperm acrosome in mouse and human spermatozoa by immunofluorescence using a specific antibody. Western blot and double staining analyses show NYD-SP27 becomes detached from sperm, as they undergo capacitation and acrosome reaction. The absence of HCO3-, a key factor in activating capacitation, from the capacitation-inducing medium prevents the loss of NYD-SP27 from sperm. The anti-NYD-SP27 antibody also prevents the loss of NYD-SP27 from sperm, reduced the number of capacitated sperm, inhibited the acrosome reaction induced by ATP and progesterone, and inhibited agonist-induced PLC-coupled Ca2+ mobilization in sperm, which can be mimicked by the PLC inhibitor, U73122. These data strongly suggest that NYD-SP27 is a physiological inhibitor of PLC that acts as an intrinsic decapacitation factor in sperm to prevent premature capacitation and acrosome reaction.


Subject(s)
Adult , Animals , Humans , Male , Mice , Middle Aged , Acrosome , Metabolism , Acrosome Reaction , Physiology , Calcium , Metabolism , Fluorescent Antibody Technique, Indirect , Immune Sera , Pharmacology , Phosphoinositide Phospholipase C , Allergy and Immunology , Metabolism , Sperm Capacitation , Physiology , Spermatozoa , Metabolism
13.
Asian Journal of Andrology ; (6): 741-748, 2008.
Article in English | WPRIM | ID: wpr-359915

ABSTRACT

<p><b>AIM</b>To investigate the expression of Spindlin 1 (Spin 1) isoform2 and assess its function in mouse testis.</p><p><b>METHODS</b>First, reverse-transcription polymerase chain reaction (RT-PCR) was used to determine whether Spin1 isoform2 is present in mouse testis. Then the expression patterns of the isoform between newborn and adult mice testes were compared by immunoblot analysis. Finally, the diversity of its localization in mice testes at different ages (days 0, 7, 14, 21, 28 and 60) was observed by immunohistochemistry. The localization of the protein in mouse sperm was also investigated by immunofluorescence.</p><p><b>RESULTS</b>The RT-PCR results show that Spin1 isoform2 is present in mouse testis. As shown by immunoblot analysis, the isoform was more highly expressed in adult testes compared with newborn testes. Interestingly, Spin1 isoform2 did not show up in the cytoplasm of primary spermatocytes until day 14. Also, the protein exists at the tail of the mouse sperm.</p><p><b>CONCLUSION</b>Spin1 isoform2 is a protein expressed highly in adult testis, which might be involved in spermatogenesis and could be necessary for normal sperm motility.</p>


Subject(s)
Animals , Female , Male , Mice , Pregnancy , Age Factors , Animals, Newborn , Blotting, Western , Cell Cycle Proteins , Genetics , Metabolism , Cytoplasm , Metabolism , Immunohistochemistry , Meiosis , Physiology , Mice, Inbred ICR , Microtubule-Associated Proteins , Genetics , Metabolism , Phosphoproteins , Genetics , Metabolism , Reverse Transcriptase Polymerase Chain Reaction , Sperm Motility , Physiology , Spermatogenesis , Physiology , Testis , Physiology
14.
National Journal of Andrology ; (12): 250-254, 2007.
Article in Chinese | WPRIM | ID: wpr-297743

ABSTRACT

Proteomics and polemic techniques are among the most valuable approaches in the research of life science in this new century, marking the beginning of a post-genome era. Two-dimensional electrophoresis and mass spectrometry, applied as key techniques in proteomic research, have given rise to new research strategies and improved the efficiency of researchers in exploring the unknown field. Its introduction into the exploration of spermatozoal proteins has given us so many pleasant surprises. This review presents some essential information about proteomics and two-dimensional electrophoresis and mass spectrometry, with a brief introduction of the recent progress in the researches on human sperm proteome, capacitation-related sperm proteins, sperm-egg interaction-related proteins, and sperm-immunity which has made great senses in the clinical problems.


Subject(s)
Humans , Male , Electrophoresis, Gel, Two-Dimensional , Proteome , Spermatozoa , Allergy and Immunology
15.
National Journal of Andrology ; (12): 87-90, 2007.
Article in Chinese | WPRIM | ID: wpr-289041

ABSTRACT

<p><b>OBJECTIVE</b>To explore the possible action mechanism of Jujingwan on asthenospermia.</p><p><b>METHODS</b>Semen routine analyses and determination of nitric oxide (NO) concentration and superoxide dismutase (SOD) activity in seminal plasma were performed in 34 cases of asthenospermia. The changes of NO concentration and SOD activity before and after the treatment with Jujingwan were observed.</p><p><b>RESULTS</b>Compared with pre-treatment, there was no significant change in NO concentration, and the activity of SOD decreased significantly after the treatment ([95.97 +/- 20.75] microg/L vs [6.14 +/- 19.99] microg/L). There was negative correlation between NO concentration and SOD activity before the treatment (r = -0.246, P < 0.05).</p><p><b>CONCLUSION</b>Jujingwan can significantly improve sperm viability in patients with asthenospermia. However, the excellent effects of Jujingwan are not displayed in the changes of NO concentration and SOD activity.</p>


Subject(s)
Adult , Humans , Male , Middle Aged , Drugs, Chinese Herbal , Pharmacology , Therapeutic Uses , Nitric Oxide , Metabolism , Oligospermia , Drug Therapy , Metabolism , Phytotherapy , Semen , Chemistry , Sperm Count , Sperm Motility , Superoxide Dismutase , Metabolism
16.
Asian Journal of Andrology ; (6): 53-59, 2006.
Article in English | WPRIM | ID: wpr-270824

ABSTRACT

<p><b>AIM</b>To study polyethylenimine (PEI)-mediated in vivo gene transfection into testis cells and preliminary functional research of spermatogenic cell-specific gene NYD-SP12 using this method.</p><p><b>METHODS</b>PEI/DNA complexes were introduced into the seminiferous tubules of mouse testes using intratesticular injection. Transfection efficiency and speciality were analyzed on the third day of transfection with fluorescent microscopy and hematoxylin staining. The long-lasting expression of the GFP-NYD-SP12 fusion protein and its subcellular localization in spermatogenic cells at different stages were analyzed with fluorescent microscopy and propidium iodide staining.</p><p><b>RESULTS</b>With the mediation of PEI, the GFP-NYD-SP12 fusion gene was efficiently transferred and expressed in the germ cells (especially in primary spermatocytes). Transfection into Sertoli cells was not observed. The subcellular localization of the GFP-NYD-SP2 fusion protein showed dynamic shifts in spermatogenic cells at different stages during spermatogenesis.</p><p><b>CONCLUSION</b>PEI can efficiently mediate gene transfer into spermatocytes. Thus, it might be useful for the functional research of spermatogenic-cell specific genes such as the NYD-SP12 gene. In our study, the NYD-SP12 protein was visualized and was involved in the formation of acrosome during spermatogenesis. Our research will continue into the detailed function of NYD-SP12 in spermatocytes.</p>


Subject(s)
Animals , Humans , Male , Mice , Green Fluorescent Proteins , Homeodomain Proteins , Genetics , Physiology , Polyethyleneimine , Spermatogenesis , Physiology , Transfection , Methods
17.
National Journal of Andrology ; (12): 1135-1138, 2006.
Article in Chinese | WPRIM | ID: wpr-289062

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of Jujingwan on the spermatozoal ultrastructure and apoptosis of germ cells in oligospermia patients.</p><p><b>METHODS</b>We treated 50 oligospermia patients with Jujingwan and observed the spermatozoal ultrastructure, the apoptosis of germ cells and the changes in the DNA ploidy proportion of spermatogenic cells by electron microscopy and FCM before the treatment and 3, 6, 9 and 12 months after it.</p><p><b>RESULTS</b>Jujingwan increased sperm acrosome base density 6 months after the treatment and remarkably improved the integrity of acrosome membrane 12 months after it, with no obvious pathological changes in the nuclei and tails. Three months after the treatment, cell debris and apoptotic cells decreased significantly as compared with pre-treatment (P < 0. 05) , and very significantly 12 months after the treatment (P <0. 01). The proportion of haploid spermatozoa increased very significantly (P <0.01) , and the lost primary spermatocytes decreased significantly (P <0. 05) compared with pre-treatment.</p><p><b>CONCLUSION</b>Jujingwan can increase the density of sperm acrosome base and improve the pathological changes of acrosome membrane in oligospermia patients; it can improve the activity of acrosome enzyme and the integrity of acrosome membrane, decrease the apoptosis rate of germ cells and sperm and increase the percentage of haploid spermatozoa; it can also reduce the percentage of apoptotic bodies and diploid sperm cells. It is indicated that Jujingwan can inhibit the apoptosis of germ cells and sperm and improve spermatogenesis in oligospermia patients.</p>


Subject(s)
Adult , Humans , Male , Acrosome , Pathology , Apoptosis , Drugs, Chinese Herbal , Therapeutic Uses , Infertility, Male , Drug Therapy , Pathology , Oligospermia , Drug Therapy , Pathology , Phytotherapy , Sperm Count , Spermatocytes , Cell Biology , Spermatozoa
18.
Asian Journal of Andrology ; (6): 277-288, 2005.
Article in English | WPRIM | ID: wpr-270848

ABSTRACT

<p><b>AIM</b>To identify a novel alternative transcript of the novel retinal pigment epithelial cell gene (NORPEG) expressed in the human testis.</p><p><b>METHODS</b>A human testis cDNA microarray was established and hybridized with cDNA probes from human fetal testes, adult testes and human spermatozoa. Differentially expressed clones were sequenced and analyzed. One of these clones was a short transcript of NORPEG which we proceeded to analyze by RT-PCR.</p><p><b>RESULTS</b>The novel short alternative transcript of NORPEG was isolated and named sNORPEG. It was 3486 bp in length and contained a 2952-bp open reading frame, encoding a 110.4-kDa protein of 983 amino acids. Amino acid sequence analysis showed that the sNORPEG protein contains six ankyrin repeats and two coiled-coil domains. It shares a high homology with the NORPEG and ankycorbin proteins in both its sequence and motifs. Blasting the human genome database localized sNORPEG to human chromosome 5p13.2-13.3. Expression profiles showed that sNORPEG was expressed in human fetal testes, adult testes and spermatozoa. Moreover, sNORPEG was found to be ubiquitously expressed in human tissues.</p><p><b>CONCLUSION</b>sNORPEG is expressed in different developmental stages of the testis and encodes a protein that may have roles in human testis development and spermatogenesis.</p>


Subject(s)
Humans , Male , Alternative Splicing , Amino Acid Sequence , Base Sequence , Cytoskeletal Proteins , Genetics , DNA, Complementary , Gene Expression Profiling , Molecular Sequence Data , Open Reading Frames , RNA, Messenger , Genetics , Reverse Transcriptase Polymerase Chain Reaction , Sequence Homology, Amino Acid , Testis , Metabolism , Transcription Factors , Genetics
19.
Asian Journal of Andrology ; (6): 245-255, 2005.
Article in English | WPRIM | ID: wpr-270850

ABSTRACT

<p><b>AIM</b>To investigate the role of a novel dipeptidyl peptidase 8 transcript variant (DPP8-v3) gene in testis development and/or spermatogenesis.</p><p><b>METHODS</b>A human testis cDNA microarray was hybridized with mRNA of human adult and fetal testes. Differentially expressed clones were sequenced and characterized and their expression was analyzed by real-time reverse transcription polymerase chain reaction (RT-PCR) and Southern-blot analysis.</p><p><b>RESULTS</b>A new transcript variant of the human dipeptidyl peptidase (DPP8), exhibiting a 5-fold higher expression level in human adult than that in fetal testes, was cloned and was named DPP8 variant 3 (DPP8-v3). The full-length sequence of DPP8-v3 was 3,030 bp, encoding a protein of 898 amino acids.</p><p><b>CONCLUSION</b>DPP8-v3 is a novel human DPP8 transcript variant highly expressed in the adult testis. Similar to DPPIV, DPP8-v3 may play a key role in the immunoregulation of testes and accordingly may influence spermatogenesis and male fertility.</p>


Subject(s)
Adult , Humans , Male , Amino Acid Sequence , Base Sequence , Blotting, Southern , DNA Primers , DNA, Complementary , Dipeptidases , Chemistry , Genetics , Gene Expression Profiling , Molecular Sequence Data , Nucleic Acid Hybridization , RNA, Messenger , Genetics , Reverse Transcriptase Polymerase Chain Reaction , Sequence Homology, Amino Acid , Testis , Embryology
20.
Asian Journal of Andrology ; (6): 179-188, 2005.
Article in English | WPRIM | ID: wpr-270855

ABSTRACT

<p><b>AIM</b>To identify a novel isoform of adaptin 2 beta subunit (named Ap2beta-NY) and to investigate its relationship with testicular development and spermatogenesis.</p><p><b>METHODS</b>Using a human testis cDNA microarray, a clone (Ap2beta-NY), which was strongly expressed in adult testes but weakly expressed in embryo testes, was sequenced and analyzed. Using polymerase chain reaction (PCR), the tissue distribution and expression time pattern of Ap2beta-NY were determined.</p><p><b>RESULTS</b>Ap2beta-NY was identified and has been deposited in the GenBank (AY341427). The expression level of Ap2beta-NY in the adult testis was about 3-fold higher than that in the embryo testis. PCR analysis using multi-tissue cDNA indicated that Ap2beta-NY was highly expressed in the testis, spleen, thymus, prostate, ovary, blood leukocyte and brain, but not in the heart, placenta, lung, liver, skeletal muscle, kidney and pancreas. In addition, Ap2beta-NY was variably expressed in the testes of patients with spermatogenesis-disturbance and spermatogenesis-arrest but not expressed in those of Sertoli-cell-only syndrome, which implied that, in the testis, Ap2beta-NY was restrictively expressed in germ cells.</p><p><b>CONCLUSION</b>Ap2beta-NY is an isoform of Ap2beta and may be involved in regulating the process of spermatogenesis and testis development.</p>


Subject(s)
Humans , Male , Adaptor Protein Complex beta Subunits , Chemistry , Genetics , Amino Acid Sequence , Base Sequence , DNA, Complementary , Molecular Sequence Data , Nucleic Acid Hybridization , Oligonucleotide Array Sequence Analysis , Polymerase Chain Reaction , RNA Splicing , RNA, Messenger , Genetics , Reverse Transcriptase Polymerase Chain Reaction , Spermatogenesis , Testis , Metabolism
SELECTION OF CITATIONS
SEARCH DETAIL