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1.
Chinese Pharmacological Bulletin ; (12): 551-556, 2019.
Article in Chinese | WPRIM | ID: wpr-857375

ABSTRACT

Aim: To explore the repair mechanism of ginsenoside Rg3 in treating the impaired diabetic wound from improving the vulnerability of diabetic skin of rats. Methods: Male SD rats (n = 32) were injected intraperitoneally streptozotocin to induce hyperglycemia, except for the rats of control group (n = 8). Diabetic rats were randomly divided into model group (equal volume of saline), aminoguanidine group (10 mg · kg-1), ginsenoside Rg3 high dose (15 mg · kg-1) and low group (5 mg · kg-1). After four weeks of oral gavage treatment, full-thickness wound was established. On 21st day after injury, wound samples were collected to observe the pathological changes in wound; the thickness of epidermis and dermis was measured by HE staining; and the epidermal cell proliferation cycle was analysed by flow cytometry; the expression of CD31 in wound tissues was detected by immunohistochemical and image analytical methods. Results: Ginsenoside Rg3 groups showed significantly more fibroblasts, necrotic tissue drops and advanced epithelial, and thickening of epidermis and dermis (P < 0. 01). Model group showed significant increase in G0/G1 phase ratio of epidermal cell cycle (P <0. 01), while reduction in G2/M and S period ratios (P < 0. 01). However, G0/G1 period ratio decreased, while G2/M and S period ratios rose in aminoguanidine group, ginsenoside Rg3 high dose and low dose groups. The decrease of G0/G1 period ratio (P < 0. 05) and increase in G2/M (P <0. 05) and S period ratios (P <0. 01) was found to be significant. The expressions of CD31 in model group was lower than those in control group (P<0. 01). Whereas, it was higher in ginsenoside Rg3 high dose group and aminoguanidine group (P < 0. 05). Conclusions: Ginsenoside Rg3 can effectively promote the repair and healing of impaired diabetic wound. The various mechanisms of repair might be through improving skin pathology, regulating epidermal cell proliferation cycle and promoting angiogenesis.

2.
National Journal of Andrology ; (12): 239-244, 2015.
Article in Chinese | WPRIM | ID: wpr-319512

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the clinical effect of microsurgical vasoepididymostomy and/or vasovasostomy in the treatment of obstructive azoospermia.</p><p><b>METHODS</b>This study included 76 patients with obstructive azoospermia, 53 treated by bilateral vasoepididymostomy (8 involving the epididymal head, 18 involving the epididymal body, 5 involving the epididymal tail, and 22 involving the epididymal head, body and tail), 14 by unilateral vasoepididymostomy, and the other 9 by unilateral vasoepididymostomy + unilateral vasovasostomy (including cross anastomosis). We followed up the patients for 2 to 16 months for the patency rate, routine semen parameters, and pregnancy outcomes.</p><p><b>RESULTS</b>The success rate of bilateral vasoepididymostomy, unilateral vasoepididymostomy, and unilateral vasoepididymostomy + unilateral vasovasostomy (including cross anastomosis) were 62.26% (33/53), 35.71% (5/14), and 77.78% (7/9), respectively. The average sperm concentrations in the three groups of patients were (27.9 +/- 5.74), (11.8 +/- 8.33), and (19.9 +/- 7.53) x 10(6)/ml, the average total sperm counts were (65.6 +/- 13.71), (28.0 +/- 15.86), and (69.2 +/- 28.59) x 10(6), and the mean rates of progressively motile sperm were (22.3 +/- 3.18), (11.0 +/- 9.77), and (15.8 +/- 5.05)%, respectively. The success rates of bilateral vasoepididymostomy that involved the epididymal head, body, tail, and all the three parts were 62.5, 72.22, 60, and 54.55%, respectively. Natural pregnancy was achieved in 8 (10.53%) of the total number of cases.</p><p><b>CONCLUSION</b>Microsurgery is effective for the treatment obstructive azoospermia. Unilateral vasoepididymostomy + unilateral vasovasostomy is superior to the other procedures, followed by bilateral vasoepididymostomy. Bilateral vasoepididymostomy involving the epididymal body may achieve a slightly better effect than that involving the other epididymal parts.</p>


Subject(s)
Adult , Female , Humans , Male , Pregnancy , Anastomosis, Surgical , Methods , Azoospermia , General Surgery , Epididymis , General Surgery , Infertility, Male , General Surgery , Microsurgery , Pregnancy Rate , Sperm Count , Treatment Outcome , Vas Deferens , General Surgery , Vasovasostomy , Methods
3.
National Journal of Andrology ; (12): 300-305, 2013.
Article in Chinese | WPRIM | ID: wpr-256917

ABSTRACT

<p><b>OBJECTIVE</b>To establish a stable and reliable model of Sertoli-cell-only syndrome in mice.</p><p><b>METHODS</b>We randomly divided 60 NIH mice into two groups of equal number to receive intraperitoneal injection of busulfan (30 mg/kg) and 30 or 60 minutes of testis cooling. At 2, 4 and 8 weeks after treatment, we recorded the survival rate of the mice, weight of the testis and Johnsen scores, and conducted quantitative analysis on the degrees of spermatogenetic failure.</p><p><b>RESULTS</b>There were no significant differences in the baseline body weight and survival rate between the intervention and control groups (P > 0.05). At 4 and 8 weeks, the testis weight and Johnsen score were significantly lower in the intervention group than in the control ([0.04 +/- 0.01] g and [0.05 +/- 0.01] g vs [0.09 +/- 0.03] g and [0.11 +/- 0.02] g, P < 0.05; 3.86 +/- 0.50 and 2.70 +/- 0.67 vs 9.60 +/- 0.25 and 9.76 +/- 0.43, P < 0.01). At 2, 4 and 8 weeks, the testis weights were (0.07 +/- 0.02) g, (0.06 +/- 0.01) g and (0.09 +/- 0.01) g, respectively, in the 30-min cooling group and (0.05 +/- 0.01) g, (0.04 +/- 0.02) g and (0.04 +/- 0.02) g in the 60-min cooling group, significantly lower than in the control side at the same time points ([0.11 +/- 0.01] g, [0.11 +/- 0.01] g and [0.12 +/- 0.00] g) (P < 0.05), and the Johnsen scores were 4.70 +/- 0.67, 2.70 +/- 0.84 and 6.10 +/- 1.14 in the 30-min and 1.67 +/- 0.58, 1.20 +/- 0.45 and 1.00 +/- 0.00 in the 60-min cooling group, remarkably lower than in the control side (9.60 +/- 3.23, 9.60 +/- 0.55 and 9.70 +/- 0.45) (P < 0.01). Histopathological examination of the cooled testes revealed considerable atrophy of seminal tubules, necrosis of seminiferous epithelia and peritubular fibrosis.</p><p><b>CONCLUSION</b>Administration of busulfan has no obvious influence on the survival of mice, and is a reliable method for constructing a mouse model of Sertoli-cell-only syndrome.</p>


Subject(s)
Animals , Male , Mice , Busulfan , Cold Temperature , Disease Models, Animal , Mice, Inbred Strains , Organ Size , Sertoli Cell-Only Syndrome , Sertoli Cells , Testis
4.
National Journal of Andrology ; (12): 311-314, 2013.
Article in Chinese | WPRIM | ID: wpr-256915

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the association between single nucleotide polymorphism (SNP) of the DZAL gene in infertile Han Chinese males with astheno-teratozoospermia.</p><p><b>METHODS</b>We collected semen samples from 173 infertile Han Chinese men with astheno-teratozoospermia (case group) and 175 age-matched normal male volunteers (control group) for semen routine and morphological analyses. We obtained genomic DNA, genotyped the polymorphisms of the DAZL gene A260G and A386G via the Sequenom MassARRAY system, and compared the frequencies of the genotypes between the case and control groups.</p><p><b>RESULTS</b>The AA nucleotide variant was found in the A260G and A386G polymorphisms of the DZAL gene in both the cases and controls, but the heterozygous AG variant in neither.</p><p><b>CONCLUSION</b>The A260G and A386G polymorphisms of the DAZL gene are not correlated with astheno-teratozoospermia-induced male infertility in the Han Chinese population, and therefore could not be considered as molecular markers of male infertility.</p>


Subject(s)
Adult , Humans , Male , Asian People , Genetics , Case-Control Studies , Genotype , Infertility, Male , Genetics , Oligospermia , Genetics , Polymorphism, Single Nucleotide , RNA-Binding Proteins , Genetics
5.
National Journal of Andrology ; (12): 1147-1149, 2010.
Article in Chinese | WPRIM | ID: wpr-266223

ABSTRACT

<p><b>OBJECTIVE</b>To explore the effects of low-dose oral tadalafil on self-esteem, confidence and sexual relationship in ED patients.</p><p><b>METHODS</b>We treated 17 ED patients with oral tadalafil at the low dose of 5 mg once daily for 12 weeks, and used the paired t test to compare their scores on The Self-Esteem and Relationship Questionnaire (SEAR) and IIEF-5 and the results of nocturnal penile tumescence (NPT) obtained by nocturnal electrobioimpedance volumetric assessment (NEVA) before and after the medication.</p><p><b>RESULTS</b>The scores on SEAR and IIEF-5 were significantly increased (P < 0.01) and NPT markedly improved (P < 0.05) after tadalafil treatment as compared with the baseline.</p><p><b>CONCLUSION</b>Low-dose oral tadalafil once daily can significantly improve the self-esteem, confidence, sexual relationship satisfaction and NPT of ED patients.</p>


Subject(s)
Adult , Humans , Male , Middle Aged , Carbolines , Therapeutic Uses , Erectile Dysfunction , Drug Therapy , Psychology , Self Concept , Surveys and Questionnaires , Tadalafil , Vasodilator Agents , Therapeutic Uses
6.
Chinese Journal of Stomatology ; (12): 92-94, 2008.
Article in Chinese | WPRIM | ID: wpr-235978

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of 17beta-estradiol on the expression of alkaline phosphatase (ALP) and osteoprotegerin in human periodontal ligament cells.</p><p><b>METHODS</b>Human periodontal ligament cells (hPDLC) were obtained from periodontal tissue explants of teeth extracted for orthodontic treatment ALP activity was determined by PNPP, and OPG protein and corresponding mRNA levels were quantitatively detected by ELISA and RT-PCR RESULTS: ALP activity was significantly increased at 14 days and 21 days (P <0.05). 17beta-E2 of physiological concentration promoted secretion of OPG protein and expression of OPG mRNA (P <0.05). 17beta-E2 with high-dose showed no effect on OPG protein secretion and decrease OPG mRNA expression.</p><p><b>CONCLUSIONS</b>17beta-E2 may have a positive impact on periodontium through promoting expression of ALP and OPG in hPDLC.</p>


Subject(s)
Humans , Alkaline Phosphatase , Metabolism , Cells, Cultured , Estradiol , Pharmacology , Osteoprotegerin , Metabolism , Periodontal Ligament , Cell Biology , Metabolism
7.
West China Journal of Stomatology ; (6): 366-369, 2004.
Article in Chinese | WPRIM | ID: wpr-330046

ABSTRACT

<p><b>OBJECTIVE</b>This study was carried out to investigate the effects of insulin-like growth factor-II (IGF-II) and basic fibroblast growth factor (bFGF) on osteoprotegerin (OPG) secretion of periodontal ligament cells (PDLCs).</p><p><b>METHODS</b>Healthy human premolars extracted for orthodontic reasons from 12-14 years old donators were obtained, and periodontal tissues were collected and cultured to obtain PDL cells. Primary or first passage PDLCs were cloned by means of limited dilutions. PDLCs with osteoblastic phenotypes were characterized as follows: Alkaline phosphatase activity, collagen III production and bone-like nodules formation. IGF-II and bFGF were added into culture media and their effects on PDLCs proliferation and OPG secretion were observed. The OPG concentrations in cell culture supernatants were detected by sandwich ELISA. Living cell numbers were demonstrated by MTT test. The average levels of OPG secretion by a single cell were calculated by dividing OPG concentration with MTT-test result.</p><p><b>RESULTS</b>Both IGF-II and bFGF upregulated the mtt values (P < 0.05), but ICF-II downregulated the opg/mtt values (P < 0.05), whereas bFGF had no significant effect on opg/mtt values (P > 0.05).</p><p><b>CONCLUSION</b>IGF-II enhances the proliferation of PDL cells but prohibits OPG secretion. Although bFGF has the same effect on the proliferation of PDL cells, it has no effect on OPG secretion. Before cytokines were used to enhance periodontal regeneration, their effects on local bone balance should also be studied.</p>


Subject(s)
Adolescent , Child , Humans , Cells, Cultured , Fibroblast Growth Factor 2 , Pharmacology , Glycoproteins , Insulin-Like Growth Factor II , Pharmacology , Osteoprotegerin , Periodontal Ligament , Cell Biology , Metabolism , Receptors, Cytoplasmic and Nuclear , Receptors, Tumor Necrosis Factor
8.
Chinese Journal of Stomatology ; (12): 288-291, 2003.
Article in Chinese | WPRIM | ID: wpr-253720

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of LPS and/or TNF-alpha on periodontal ligament cell (PDLC) proliferation and OPG secretion.</p><p><b>METHODS</b>Healthy premolars extracted for orthodontic reasons from a 12 years old boy were obtained, and periodontal tissues were collected and cultured to obtain PDLCs. Cloned PDLCs were obtained by means of limited dilutions, and were characterized as follows: alkaline phosphatase activity, collagen III production and bone-like nodules formation. LPS and rhTNF-alpha were added into culture media and their effects on PDLC proliferation and OPG secretion were observed. The OPG concentrations in cell culture supernatants were detected by sandwich ELISA. Living cell numbers were demonstrated by MTT test. The average levels of OPG secretion by a single cell were calculated by dividing OPG concentration with MTT result.</p><p><b>RESULTS</b>rhTNF-alpha above 10 micro g/L decreased the mtt and opg detecting results, but increased the opg/mtt values (P < 0.05). However, LPS had no effect on mtt, opg or opg/mtt values. Neither it had any interaction with rhTNF-alpha (P > 0.05).</p><p><b>CONCLUSIONS</b>TNF-alpha prohibits the proliferation of PDLCs but enhances their OPG secretion. However, LPS has no effect on neither side. Our works support the hypothesis that there may be an inverse feedback regulation pattern of increasing periodontal OPG production against local bone resorption activity. PDLCs might not be the natural target cells of LPS' direct cytotoxic effect.</p>


Subject(s)
Child , Humans , Male , Glycoproteins , In Vitro Techniques , Lipopolysaccharides , Pharmacology , Osteoprotegerin , Periodontal Ligament , Metabolism , Pathology , Receptors, Cytoplasmic and Nuclear , Receptors, Tumor Necrosis Factor , Tumor Necrosis Factor-alpha , Pharmacology
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