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1.
Anat Rec (Hoboken) ; 306(12): 3021-3032, 2023 12.
Article in English | MEDLINE | ID: mdl-35661433

ABSTRACT

Asthenozoospermia is a leading cause of male infertility, characterized by reduced sperm motility. In this study, we determined sperm motility and the activities of antioxidant enzymes and oxidation products in the testis of rats with ornidazole (ORN)-induced asthenozoospermia and further examined and compared the differential effects of moxa smoke (MS) and cigarette smoke (CS) on sperm motility and oxidative stress (OS) of asthenozoospermic rats. The smoke intervention was initiated 11 days after intragastric administration of ORN, followed by the examination of testis index, sperm parameters, OS-related gene levels, and testicular histopathology. Sperm motility and antioxidant enzyme activities, as well as oxidation products significantly decreased in ORN-induced rats compared with MS-treated rats (p < .05-.001). MS treatment restored the reduced sperm motility and activities of glutathione peroxidase, superoxide dismutase, and catalase, but increased the malondialdehyde and nitric oxide synthetase levels in ORN-induced rats (p < .05-.001). Also, the histopathological changes in the testis of ORN-induced rats were improved by MS treatment. The study highlighted that MS was an effective factor in moxibustion therapy, which notably improved the sperm motility of asthenozoospermic rats by inhibiting OS in the reproductive system.


Subject(s)
Asthenozoospermia , Ornidazole , Humans , Rats , Male , Animals , Antioxidants/pharmacology , Asthenozoospermia/chemically induced , Asthenozoospermia/metabolism , Asthenozoospermia/pathology , Sperm Count , Sperm Motility , Semen , Spermatozoa , Testis/metabolism , Oxidative Stress , Ornidazole/adverse effects , Ornidazole/metabolism
2.
PLoS One ; 16(6): e0252906, 2021.
Article in English | MEDLINE | ID: mdl-34153045

ABSTRACT

Oligoasthenozoospermia is a complex disease caused by a variety of factors, and its incidence is increasing yearly worldwide. Yishen Tongluo formula (YSTLF), created by Professor Sun Zixue, has been used to treat oligoasthenozoospermia in clinical practice for several decades with a good therapeutic effect. However, the chemical and pharmacological profiles of YSTLF remain unclear and need to be elucidated. In this study, a network pharmacology approach was applied to explore the potential mechanisms of YSTLF in oligoasthenozoospermia treatment. All of the compounds in YSTLF were retrieved from the corresponding databases, and the bioactive ingredients were screened according to their oral bioavailability (OB) and drug-likeness (DL). The potential proteins of YSTLF were obtained from the traditional Chinese medicine systems pharmacology (TCMSP) database and the Bioinformatics Analysis Tool for Molecular Mechanism of Traditional Chinese Medicine (BATMAN-TCM) database, while the potential genes of oligoasthenozoospermia were obtained from the GeneCards database and the DisGeNET database. The STRING database was used to construct an interaction network according to the common targets identified by the online tool Venny for YSTLF and oligoasthenozoospermia. The topological characteristics of nodes were visualized and analyzed through Cytoscape. Biological functions and significant pathways were determined and analyzed using the Gene Ontology (GO) knowledgebase, the Kyoto Encyclopedia of Genes and Genomes (KEGG) and Metascape. Finally, the disease-formula-compound-target-pathway network was constructed by Cytoscape. A total of 106 bioactive ingredients and 134 potential targets from YSTLF were associated with oligoasthenozoospermia or considered to be therapeutically relevant. Pathway analysis indicated that the PI3K/Akt, MAPK and apoptosis signaling pathways were significant pathways involved in oligoasthenozoospermia. In conclusion, the current study expounded the pharmacological actions and molecular mechanisms of YSTLF in treating oligoasthenozoospermia from a holistic viewpoint. The potential molecular mechanisms were closely related to antioxidative stress, antiapoptosis and anti-inflammation, with TNF, CCND1, ESR1, NFKBIA, NR3C1, MAPK8, and IL6 being possible targets. This network pharmacology prediction may offer a helpful tool to illustrate the molecular mechanisms of the Chinese herbal compound YSTLF in oligoasthenozoospermia treatment.


Subject(s)
Asthenozoospermia/drug therapy , Drugs, Chinese Herbal/chemistry , Gene Regulatory Networks/drug effects , Oligospermia/drug therapy , Phytochemicals/pharmacology , Protein Interaction Maps/drug effects , Asthenozoospermia/genetics , Asthenozoospermia/metabolism , Asthenozoospermia/pathology , Computational Biology , Gene Ontology , Humans , Male , Molecular Docking Simulation , Oligospermia/genetics , Oligospermia/metabolism , Oligospermia/pathology
3.
J Assist Reprod Genet ; 36(2): 255-266, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30284103

ABSTRACT

PURPOSE: Motility of spermatozoa helps not only in planning the type of infertility treatment but also directly reflects the success rate in assisted reproductive technology (ART). Previously, biotin, a water-soluble vitamin, has been shown to increase the motility and longevity of cryopreserved human spermatozoa. The present study was designed to understand the molecular basis of the beneficial effects of presence of biotin in sperm wash medium on early embryo development. METHODS: The effect biotin supplementation to sperm wash medium on the sperm parameters were assessed in swim-up fraction of normozoospermic and asthenozoospermic ejaculates collected from infertile men. Fertilization and early embryo development was studied using Swiss albino mice. RESULTS: Even though both biotin and pentoxifylline (PTX) enhanced the motility of spermatozoa from normozoospermic and asthenozoospermic samples, biotin group exhibited higher in vitro survival. Using mouse model, we observed that presence of biotin or PTX in sperm wash medium improved the fertilization rate and blastocyst rate compared to control. Blastocysts from these groups had significantly higher total cell number (P < 0.01) and lower apoptotic index. In silico target prediction revealed that GTPase HRas (HRas), tyrosine-protein phosphatase nonreceptor type 1 (PTP1B), and glucokinase are the probable targets for biotin. Solution-state Nuclear Magnetic Resonance (NMR) studies confirmed that biotin interacts both with human HRas and PTP1B. CONCLUSION: Our results indicate that presence of biotin in sperm wash medium can improve the fertilization potential and preimplantation embryo development and can be considered as a safe alternate to PTX.


Subject(s)
Asthenozoospermia/drug therapy , Culture Media/chemistry , Embryonic Development/drug effects , Spermatozoa/growth & development , Animals , Asthenozoospermia/pathology , Biotin/pharmacology , Blastocyst/drug effects , Cryopreservation , Female , Fertilization/drug effects , Fertilization in Vitro/drug effects , Gene Expression Regulation, Developmental/drug effects , Glucokinase/genetics , Humans , Male , Mice , Pentoxifylline/pharmacology , Pregnancy , Protein Tyrosine Phosphatase, Non-Receptor Type 1/genetics , Sperm Motility/drug effects , Spermatozoa/drug effects
4.
Reproduction ; 155(4): 383-392, 2018 04.
Article in English | MEDLINE | ID: mdl-29581387

ABSTRACT

Asthenozoospermia is one of the leading causes of male infertility owing to a decline in sperm motility. Herein, we determined if there is a correlation between RNASET2 content on human spermatozoa and sperm motility in 205 semen samples from both asthenozoospermia patients and normozoospermia individuals. RNASET2 content was higher in sperm from asthenozoospermia patients than in normozoospermia individuals. On the other hand, its content was inversely correlated with sperm motility as well as progressive motility. Moreover, the inhibitory effect of RNASET2 on sperm motility was induced by incubating normozoospermic sperm with RNase T2 protein. Such treatment caused significant declines in intracellular spermatozoa PKA activity, PI3K activity and calcium level, which resulted in severely impaired sperm motility, and the sperm motility was largely rescued by cAMP supplementation. Finally, protein immunoprecipitation and mass spectrometry identified proteins whose interactions with RNASET2 were associated with declines in human spermatozoa motility. AKAP4, a protein regulating PKA activity, coimmunoprecipated with RNASET2 and they colocalized with one another in the sperm tail, which might contribute to reduced sperm motility. Thus, RNASET2 may be a novel biomarker of asthenozoospermia. Increases in RNASET2 can interact with AKAP4 in human sperm tail and subsequently reduce sperm motility by suppressing PKA/PI3K/calcium signaling pathways.


Subject(s)
A Kinase Anchor Proteins/metabolism , Asthenozoospermia/pathology , Calcium/metabolism , Cyclic AMP-Dependent Protein Kinases/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Ribonucleases/metabolism , Sperm Motility/physiology , Tumor Suppressor Proteins/metabolism , Adult , Asthenozoospermia/metabolism , Biomarkers/analysis , Case-Control Studies , Humans , Male , Signal Transduction , Spermatozoa/metabolism , Spermatozoa/pathology , Young Adult
5.
Andrologia ; 46(9): 956-62, 2014.
Article in English | MEDLINE | ID: mdl-24147895

ABSTRACT

We investigated the effects of folic acid and zinc sulphate supplementation on the improvement of sperm function in subfertile oligoasthenoteratozoospermic (OAT) men. Eighty-three OAT men participated in a 16-week intervention randomised, double-blind clinical trial with daily treatment of folic acid (5 mg day(-1) ) and zinc sulphate (220 mg day(-1) ), or placebo. Before and after treatment, semen and blood samples were obtained for determining sperm concentration, motility, and morphology, sperm viability, sperm mitochondrial function, sperm chromatin status using toluidine blue, aniline blue, acridine orange and chromomycin A3 staining; and semen and blood folate, zinc, B12 , total antioxidant capacity (TAC) and malondialdehyde (MDA) concentrations. Sperm concentration (×10(6)  ml(-1) ) increased in subfertile men receiving the combined treatment of folic acid and zinc sulphate and also in the group receiving only folic acid treatment; however, it was not statistically significant (P = 0.056 and P = 0.05, respectively). Sperm chromatin integrity (%) increased significantly in subfertile men receiving only zinc sulphate treatment (P = 0.048). However, this improvement in sperm quality was not significant after adjusting placebo effect. This study showed that zinc sulphate and folic acid supplementation did not ameliorate sperm quality in infertile men with severely compromised sperm parameters, OAT. Male infertility is a multifactorial disorder, and also nutritional factors play an important role in results of administration of supplementation on sperm parameters. However, these results should be confirmed by multiple studies in larger populations of OAT men.


Subject(s)
Asthenozoospermia/drug therapy , Folic Acid/therapeutic use , Micronutrients/therapeutic use , Oligospermia/drug therapy , Zinc Sulfate/therapeutic use , Antioxidants/metabolism , Asthenozoospermia/pathology , Asthenozoospermia/physiopathology , Chromatin/drug effects , Chromatin/metabolism , Dietary Supplements , Double-Blind Method , Folic Acid/administration & dosage , Humans , Male , Malondialdehyde/metabolism , Micronutrients/administration & dosage , Oligospermia/pathology , Oligospermia/physiopathology , Sperm Count , Sperm Motility/drug effects , Spermatozoa/abnormalities , Spermatozoa/drug effects , Spermatozoa/physiology , Zinc Sulfate/administration & dosage
6.
Zhonghua Nan Ke Xue ; 19(5): 446-50, 2013 May.
Article in Chinese | MEDLINE | ID: mdl-23757970

ABSTRACT

OBJECTIVE: To study the effects of Wuzi Yanzong Pills (WYP) on sperm mitochondrial membrane potential (MMP) and its ultrastructure in oligo-asthenozoospermia model rats. METHODS: Oligo-asthenozoospermia models were made in 50 male rats weighing 200 - 220 g by intragastric administration of Tripterygium Glucosides at 30 mg per kg per d for 8 weeks, and then equally allocated to a model control, a Huangjing Zanyu Capsule (HZC) control, a low-dose WYP, a medium-dose WYP, and a high-dose WYP group. Another 10 age-matched normal male rats were included as normal controls. The rats in the model and normal control groups were given intragastrically distilled water at 10 ml/kg, those in the HZC group administered HZC at 3.01 g/kg, and those in the low-, medium- and high-dose WYP groups medicated with WYP at 2.30, 4.60 and 9.20 g/kg, respectively, once daily for 30 days. At 30 minutes after the last administration, we detected the sperm MMP by JC-1 fluorescent staining and flow cytometry, and examined the sperm ultrastructure under the JEM-1230 transmission electron microscope. RESULTS: JC-1 + % and its fluorescence intensity were (33.77 +/- 6.19)% and 1 468 +/- 496 in the model control, (56.34 +/- 10.35)% and 3 277 +/- 895 in the HZC control, (40.80 +/- 10.40)% and 2 016 +/- 767 in the low-dose WYP, (59.40 +/- 6.51)% and 3 897 +/- 643 in the medium-dose WYP, and (60.71 +/- 7.81)% and 3 371 +/- 647 in the high-dose WYP group, significantly reduced in comparison with (70.80 +/- 4.92)% and 4 360 +/- 945 in the normal control group (P < 0.05), but remarkably higher in the medium- and high-dose WYP groups than in the model controls (P < 0. 05). After modeling, the sperm membrane was loose and degenerated, the mitochondria swelling, variously sized and with incomplete membrane, and the axonemal structure unclear or ruptured. After 30 days of WYP administration, compared with the model control group, the rats exhibited integrated sperm membrane and mitochondrial membrane, reduced mitochondrial swelling and basically normal axonemal and microtubular structures. CONCLUSION: Tripterygium Glucosides could decrease the sperm mitochondrial membrane potential and damage the mitochondrial structure, while WYP could significantly increase the sperm mitochondrial membrane potential and reduce the sperm mitochondrial structure damage. The protection of the integrity of sperm mitochondrial structure and function is one of the mechanisms of WYP acting on oligo-asthenozoospermia.


Subject(s)
Asthenozoospermia , Drugs, Chinese Herbal/pharmacology , Membrane Potential, Mitochondrial/drug effects , Oligospermia , Spermatozoa/drug effects , Animals , Asthenozoospermia/pathology , Asthenozoospermia/physiopathology , Male , Oligospermia/pathology , Oligospermia/physiopathology , Rats , Rats, Sprague-Dawley , Spermatozoa/physiology , Spermatozoa/ultrastructure
7.
Zhonghua Nan Ke Xue ; 18(11): 1045-9, 2012 Nov.
Article in Chinese | MEDLINE | ID: mdl-23214258

ABSTRACT

OBJECTIVE: To investigate the effects of Yijing Recipe on sperm apoptosis and mitochondrial membrane potential (MMP) in patients with idiopathic oligoathenoteratospermia. METHODS: Using the self-control method, we examined sperm apoptosis and MMP in 30 patients with oligoathenoteratospermia before and after treated with Yijing Recipe. RESULTS: The rates of early sperm apoptosis (AV +/PI -) and MMP loss were significantly reduced after treatment as compared with pre-medication ([2.86 +/- 1.47]% vs [4.26 +/- 2.79]% and [21.77 +/- 13.46]% vs [41.73 +/- 20.30]%, P<0.05). No statistically significant difference was observed in the sperm death rate (PI+) before and after treatment ([34.10 +/- 16.26]% vs [30.21 +/- 13.50]%, P>0.05). CONCLUSION: Yijing Recipe can reduce early sperm apoptosis and improve MMP, which may be one of the mechanisms underlying its efficacy on oligoathenoteratospermia.


Subject(s)
Apoptosis/drug effects , Asthenozoospermia/drug therapy , Drugs, Chinese Herbal/therapeutic use , Membrane Potential, Mitochondrial/drug effects , Oligospermia/drug therapy , Phytotherapy , Adult , Asthenozoospermia/pathology , Asthenozoospermia/physiopathology , Humans , Infertility, Male/drug therapy , Infertility, Male/pathology , Infertility, Male/physiopathology , Male , Oligospermia/pathology , Oligospermia/physiopathology , Semen Analysis , Sperm Motility , Spermatozoa
9.
Andrologia ; 43(1): 38-47, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21219381

ABSTRACT

Effective medical treatments of infertile men with idiopathic oligoasthenoteratospermia (OAT) have yet to be determined. This study considered two major aims: (i) to measure the changes in semen parameters, omega-3 fatty acids (FA) compositions and anti-oxidant activity; (ii) to determine if the administration of omega-3 FA affect semen quality in infertile men with OAT. Two hundred thirty-eight infertile men with idiopathic OAT were randomised to eicosapentaenoic (EPA) and docosahexaenoic acids (DHA), 1.84 g per day (EPAX 5500TG; Lysaker, Norway), or placebo for 32 weeks. The semen parameters were assessed according to WHO criteria, and the EPA and DHA concentrations were determined in red blood cells (RBCs), seminal plasma and sperm cells at baseline and 32-week treatment period. Of randomised subjects, 211 (88.7%) completed the full 32-week randomisation period. The anti-oxidant status of seminal plasma was also evaluated by measuring the superoxide dismutase (SOD) and catalase-like activity. In the total group of participants, all EPA and DHA levels in RBC, and seminal plasma, were statistically significantly correlated with those in spermatozoa (both P = 0.001). A significant improvement of sperm cell total count (from 38.7 ± 8.7 ' 106 to 61.7 ± 11.2 ' 106, P = 0.001) and sperm cell concentration (from 15.6 ± 4.1 ' 106 per ml to 28.7 ± 4.4 ' 106 per ml, P = 0.001) was observed in the omega-3 group. A significant positive correlation was found between the EPA and DHA in seminal plasma and the semen parameters. Seminal plasma EPA and DHA concentrations were positively correlated with seminal plasma SOD-like and catalase-like activity (both P = 0.001). In seminal plasma, both SOD-like and catalase-like activity were positively correlated with sperm count, sperm motility, and sperm morphology. Oligoasthenoteratospermic men with low levels of EPA and DHA may benefit from omega-3 FA supplementation. Further studies are warranted to shed more light on this important issue.


Subject(s)
Asthenozoospermia/enzymology , Asthenozoospermia/pathology , Fatty Acids, Omega-3/pharmacology , Infertility, Male/enzymology , Infertility, Male/pathology , Semen/drug effects , Semen/enzymology , Adult , Asthenozoospermia/drug therapy , Catalase/metabolism , Dietary Supplements , Docosahexaenoic Acids/administration & dosage , Docosahexaenoic Acids/pharmacology , Docosahexaenoic Acids/therapeutic use , Dose-Response Relationship, Drug , Double-Blind Method , Eicosapentaenoic Acid/administration & dosage , Eicosapentaenoic Acid/pharmacology , Eicosapentaenoic Acid/therapeutic use , Fatty Acids, Omega-3/administration & dosage , Fatty Acids, Omega-3/therapeutic use , Humans , Infertility, Male/drug therapy , Male , Semen/cytology , Sperm Count , Sperm Motility/drug effects , Spermatozoa/drug effects , Spermatozoa/pathology , Superoxide Dismutase/metabolism
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