Shi Zhicheng, Enayatullah Hamdard, Lv Zengpeng, Dai Hongjian, Wei Quanwei, Shen Lirong, Karwand Babrak, Shi Fangxiong
College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
College of Food Science, Zhejiang University, Hangzhou 310058, China.
Animals (Basel). 2019 Nov 15;9(11):977. doi: 10.3390/ani9110977.
Spermatogenesis and hormones secretions are crucial endocrine and physiological process for maintaining the life. Royal Jelly (RJ) bioactive components are Major Royal Jelly Proteins (MRJPs), owing exceptional biological properties. However, the effects of RJ on pup's testicular development during neonatal and pubertal period exposure hasn't been adequately studied. The aim of the study was to detect neonatal sexual hormones concentration and histopathological changes on testicular development of the male progeny after oral exposure to freeze-dried RJ for 35 consecutive days. After mice give birth, male pups were collected together, separated by sex, and randomly standardized to seven (7) male pups per dam. Male pups were assigned to control diet (CON group), low dose RJ (L-RJ group) diet (control diet + 125 mg/kg/day RJ), moderate dose RJ (M-RJ group) diet (control diet + 250 mg/kg/day RJ) and high dose of RJ (H-RJ group) diet (control diet + 500 mg/kg/day RJ). After weaning, male pups were continuously fed with freeze-dried RJ until the age of PNDs 35. The results revealed that, oral M-RJ (250 mg/kg/day) administration significantly ( < 0.05) increased the testis weight, the diameter of seminiferous tubule and the height of seminiferous epithelium of offspring mice at PNDs 14. However, high-dose RJ (500 mg/kg/day) decreased the diameter of seminiferous tubule but increased the height of seminiferous epithelium of male offspring ( < 0.05) at the same time point. Furthermore, oral M-RJ treatment significantly ( < 0.05) increased the testis weight and spermatogenesis at PNDs 21. Whereas, oral H-RJ treatment significantly ( < 0.05) reduced the diameter of seminiferous tubule and the height of seminiferous epithelium at PNDs 21. At PNDs 35, oral M-RJ treatment increased the testis weight, the diameter of seminiferous tubule and the level of FSH. While, high-dose of RJ reduced testis weight and size (diameter of seminiferous tubule and height of seminiferous epithelium), ratio of apoptotic germ cells and incomplete spermatogenesis collectively. In addition, sexual hormone secretions (FSH, LH, E2) were decreased after RJs treatment (L-RJ, M-RJ, H-RJ) at PNDs 21 respectively. In conclusion, the results concluded that oral administration of low and moderate doses of RJ could enhance the development of testis at neonate period until pubescent, whereas unfavorable adverse effects induced by high dose of RJ might remain.
精子发生和激素分泌是维持生命至关重要的内分泌和生理过程。蜂王浆(RJ)的生物活性成分是主要蜂王浆蛋白(MRJPs),具有卓越的生物学特性。然而,RJ对新生期和青春期暴露的幼崽睾丸发育的影响尚未得到充分研究。本研究的目的是检测连续35天口服冻干RJ后雄性后代的新生性激素浓度以及睾丸发育的组织病理学变化。小鼠分娩后,将雄性幼崽集中收集,按性别分开,每只母鼠随机标准化为7只雄性幼崽。雄性幼崽被分配到对照饮食组(CON组)、低剂量RJ饮食组(L-RJ组,对照饮食 + 125毫克/千克/天RJ)、中剂量RJ饮食组(M-RJ组,对照饮食 + 250毫克/千克/天RJ)和高剂量RJ饮食组(H-RJ组,对照饮食 + 500毫克/千克/天RJ)。断奶后,雄性幼崽持续喂食冻干RJ直至出生后第35天(PNDs 35)。结果显示,口服中剂量RJ(250毫克/千克/天)在出生后第14天显著(<0.05)增加了后代小鼠的睾丸重量、曲细精管直径和生精上皮高度。然而,在同一时间点,高剂量RJ(500毫克/千克/天)降低了雄性后代曲细精管直径,但增加了生精上皮高度(<0.05)。此外,口服中剂量RJ治疗在出生后第21天显著(<0.05)增加了睾丸重量和精子发生。而口服高剂量RJ治疗在出生后第21天显著(<0.05)降低了曲细精管直径和生精上皮高度。在出生后第3个月,口服中剂量RJ治疗增加了睾丸重量、曲细精管直径和促卵泡生成素(FSH)水平。而高剂量RJ共同降低了睾丸重量和大小(曲细精管直径和生精上皮高度)、凋亡生殖细胞比例和不完全精子发生。此外,在出生后第21天,RJ治疗组(L-RJ、M-RJ、H-RJ)的性激素分泌(FSH、促黄体生成素(LH)、雌二醇(E2))分别降低。总之,结果表明,口服低剂量和中剂量RJ可促进新生期至青春期睾丸的发育,而高剂量RJ可能会产生不利的不良影响。