1.Status quo of the researches on the biological effect of electromagnetic radiation on the testis and epididymal sperm.
Xiao-fang GAO ; Shui-ming WANG ; Rui-yun PENG
National Journal of Andrology 2007;13(9):826-829
The testis is highly sensitive to electromagnetic radiation. Sperm is the passer of male genetic material and electromagnetic radiation may cause structural and functional injury to the testis, including motility reduction, abnormality increase and ultrastructural alteration of epididymal sperm. Energy metabolism disorder in spermatogenic cells, enhancement of lipid peroxidation in the testis, excessive expression of inflammatory factors and abnormality of genetic transcription may be responsible for injury to the testis and epididymal sperm. This paper reviews the progress made in this field and the preventive measures against the injury.
Animals
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Epididymis
;
radiation effects
;
Humans
;
Male
;
Radiation
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Rats
;
Rats, Sprague-Dawley
;
Sperm Count
;
Sperm Motility
;
radiation effects
;
Testis
;
radiation effects
2.Impact of cell phone radiation on male reproduction.
Ning KANG ; Xue-Jun SHANG ; Yu-Feng HUANG
National Journal of Andrology 2010;16(11):1027-1030
With the popularized use cell phones, more and more concern has been aroused over the effects of their radiation on human health, particularly on male reproduction. Cell phone radiation may cause structural and functional injuries of the testis, alteration of semen parameters, reduction of epididymal sperm concentration and decline of male fertility. This article presents an overview on the impact of cell phone radiation on male reproduction.
Cell Phone
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DNA Damage
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Epididymis
;
radiation effects
;
Humans
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Male
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Oxidative Stress
;
Semen
;
radiation effects
;
Sperm Count
;
Sperm Motility
;
radiation effects
;
Testis
;
radiation effects
3.Circadian effects of ionizing radiation on reproductive function and clock genes expression in male mouse.
Fenju QIN ; Ningang LIU ; Jing NIE ; Tao SHEN ; Yingjie XU ; Shuxian PAN ; Hailong PEI ; Guangming ZHOU
Environmental Health and Preventive Medicine 2021;26(1):103-103
BACKGROUND:
Exposure to the ionizing radiation (IR) encountered outside the magnetic field of the Earth poses a persistent threat to the reproductive functions of astronauts. The potential effects of space IR on the circadian rhythms of male reproductive functions have not been well characterized so far.
METHODS:
Here, we investigated the circadian effects of IR exposure (3 Gy X-rays) on reproductive functional markers in mouse testicular tissue and epididymis at regular intervals over a 24-h day. For each animal, epididymis was tested for sperm motility, and the testis tissue was used for daily sperm production (DSP), testosterone levels, and activities of testicular enzymes (glucose-6-phosphate dehydrogenase (G6PDH), sorbitol dehydrogenase (SDH), lactic dehydrogenase (LDH), and acid phosphatase (ACP)), and the clock genes mRNA expression such as Clock, Bmal1, Ror-α, Ror-β, or Ror-γ.
RESULTS:
Mice exposed to IR exhibited a disruption in circadian rhythms of reproductive markers, as indicated by decreased sperm motility, increased daily sperm production (DSP), and reduced activities of testis enzymes such as G6PDH, SDH, LDH, and ACP. Moreover, IR exposure also decreased mRNA expression of five clock genes (Clock, Bmal1, Ror-α, Ror-β, or Ror-γ) in testis, with alteration in the rhythm parameters.
CONCLUSION
These findings suggested potential health effects of IR exposure on reproductive functions of male astronauts, in terms of both the daily overall level as well as the circadian rhythmicity.
ARNTL Transcription Factors/genetics*
;
Acid Phosphatase
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Animals
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CLOCK Proteins/genetics*
;
Circadian Rhythm/radiation effects*
;
Epididymis/radiation effects*
;
Gene Expression/radiation effects*
;
Genitalia, Male/radiation effects*
;
Glucosephosphate Dehydrogenase
;
L-Iditol 2-Dehydrogenase
;
L-Lactate Dehydrogenase
;
Male
;
Mice
;
Mice, Inbred C57BL
;
Models, Animal
;
Nuclear Receptor Subfamily 1, Group F, Member 1/genetics*
;
Nuclear Receptor Subfamily 1, Group F, Member 2/genetics*
;
Nuclear Receptor Subfamily 1, Group F, Member 3/genetics*
;
RNA, Messenger/genetics*
;
Radiation Exposure
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Radiation, Ionizing
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Reproductive Physiological Phenomena/radiation effects*
;
Sperm Motility/radiation effects*
;
Spermatozoa/radiation effects*
;
Testis/radiation effects*
4.Protective effect of astaxanthin against epididymal oxidative damagein rats with ornidazole-induced oligoasthenozoospermia.
Wei LIU ; Xiao-Fang KANG ; Guo-Wei ZHANG ; Hong-Cai CAI ; Kai-Qiang LI ; Ling-Ling WANG ; Xue-Jun SHANG
National Journal of Andrology 2017;23(3):206-211
Objective:
To investigate the improving effect of astaxanthin (AST) on the sperm quality of rats with ornidazole (ORN)-induced oligoasthenozoospermiaand its action mechanism.
METHODS:
Forty adult male SD rats were equally randomized into groups A (solvent control), B (low-dose ORN [400 mg/(kg·d)]), C (high-dose ORN [800 mg/(kg·d)]), D (low-dose ORN [400 mg/(kg·d)] + AST [20 mg/(kg·d)]), and E (high-dose ORN [800 mg/(kg·d)] + AST [20 mg/(kg·d)]), all treated intragastrically for3 weeks.After treatment, the epididymal tails ononeside was taken for determination of sperm concentration and activity, and the epididymideson the other side harvested for measurement of the activities of GSH-Px, GR, CAT and SOD and the MDA contentin the homogenate.
RESULTS:
Compared with group A, sperm motilityin the epididymal tail andGSH-Px and SOD activities in theepididymiswere markedly decreased while the MDAcontent significantlyincreased in group B (P<0.05), spermmotility and concentrationin the epididymal tail, testisindex, and the activities of GSH-Px, GR, CAT and SOD in the epididymis were remarkably reduced while theMDA contentsignificantly increased in group C(P<0.05). In comparison with group B, group D showed markedly increased sperm motility ([45.3±8.7]% vs [66.3±8.9]%, P<0.05) in the epididymal tail and SOD activity in the epididymis ([116.7±25.3] U/mg prot vs [146.1±23.8] U/mg prot, P<0.05), decreased MDA content([1.68±0.45] nmol/mg prot vs [1.19±0.42] nmol/mg prot, P<0.05).Compared with group C, group Eexhibited significant increases in the weight gained ([89.0±9.5] vs [99.9±4.1] %, P<0.05) and sperm motility ([17.9±3.5]% vs [27.3±5.3] %, P<0.05) but a decrease in the content of MDA ([2.03±0.30] nmol/mg prot vs [1.52±0.41] nmol/mg prot, P<0.05).
CONCLUSIONS
AST can improve spermquality in rats with ORN-inducedoligoasthenozoospermia, which may be associated with its enhancing effect on the antioxidant capacity of the epididymis.
Animals
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Antioxidants
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pharmacology
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Asthenozoospermia
;
prevention & control
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Epididymis
;
drug effects
;
metabolism
;
Male
;
Oligospermia
;
prevention & control
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Ornidazole
;
Oxidative Stress
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Protective Agents
;
pharmacology
;
Radiation-Sensitizing Agents
;
Random Allocation
;
Rats
;
Rats, Sprague-Dawley
;
Sperm Count
;
Sperm Motility
;
Spermatozoa
;
drug effects
;
metabolism
;
Xanthophylls
;
pharmacology