Amelioration of titanium dioxide nanoparticle reprotoxicity by the antioxidants morin and rutin

被引:50
作者
Hussein, Mohamed M. A. [1 ]
Gad, Emad [2 ]
Ahmed, Mona M. [3 ]
Arisha, Ahmed H. [5 ]
Mahdy, Hasnaa F. [2 ]
Swelum, Ayman Abdel-Aziz [4 ,6 ]
Tukur, Hammed A. [4 ]
Saadeldin, Islam M. [4 ,5 ]
机构
[1] Zagazig Univ, Fac Vet Med, Dept Biochem, Zagazig 44519, Egypt
[2] Suez Canal Univ, Fac Sci, Dept Chem, Ismailia, Egypt
[3] Zagazig Univ, Fac Vet Med, Dept Forens Med & Toxicol, Zagazig 44519, Egypt
[4] King Saud Univ, Coll Food & Agr Sci, Dept Anim Prod, Riyadh 11451, Saudi Arabia
[5] Zagazig Univ, Fac Vet Med, Dept Physiol, Zagazig 44519, Egypt
[6] Zagazig Univ, Fac Vet Med, Dept Theriogenol, Zagazig 44519, Egypt
关键词
Titaniumdioxide nanoparticles; Rutin; Morin; Reproduction; Male; Rats; TETRACHLORIDE-INDUCED HEPATO; OXIDATIVE STRESS; PROTECTIVE ROLE; SILVER NANOPARTICLES; REACTIVE OXYGEN; DNA-DAMAGE; TOXICITY; TESTIS; CELLS; SPERMATOGENESIS;
D O I
10.1007/s11356-019-06091-0
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The present study aimed to examine the ameliorative effects of morin and rutin on the reproductive toxicity induced by titanium dioxide nanoparticles (TiO(2)NPs) in male rats. A total of seventy adult male Sprague-Dawley rats were randomly divided into seven groups, each comprising ten rats. Nanoreprotoxicity was induced by treating rats with TiO(2)NPs at a dosage of 300 mg/kg body weight for 30 days. Morin (30 mg/kg body weight) and rutin (100 mg/kg body weight) were co-administered with or without TiO(2)NPs to rats either individually or combined. Only distilled water was administered to the control group. The results showed that TiO(2)NPs enhanced oxidative stress, indicated by reduced levels of antioxidants such as superoxide dismutase (SOD), catalase (CAT), and glutathione (GSH) in testicular tissues, and increased levels of the lipid peroxidation marker malondialdehyde (MDA). TiO(2)NPs significantly reduced the levels of sex hormones (testosterone, FSH, and LH), reduced sperm motility, viability, and sperm cell count, and increased sperm abnormalities, in addition to damaging the testicular histological architecture. TiO(2)NPs resulted in the downregulation of 17 beta-HSD and the upregulation of proapoptotic gene (Bax) transcripts in the testicular tissues. Conversely, morin and/or rutin had a protective effect on testicular tissue. They effectively counteracted TiO2NP-induced oxidative damage and morphological injury in the testis by conserving the endogenous antioxidant mechanisms and scavenging free radicals. Thus, we suggest that morin and rutin could be used to alleviate the toxicity and oxidative damage associated with TiO2NP intake.
引用
收藏
页码:29074 / 29084
页数:11
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