Mitsui Yukio, Bagchi Manashi, Marone Palma Ann, Moriyama Hiroyoshi, Bagchi Debasis
Horus Co., Ltd. , Tokyo , Japan .
Toxicol Mech Methods. 2015 Jan;25(1):13-20. doi: 10.3109/15376516.2014.971139. Epub 2014 Oct 20.
Placenta is an important organ that connects the developing fetus to allow nutrient uptake, antibody provisions and gas exchange via the blood supply of the mother. We developed a novel, standardized, stable, water-soluble, peptide-enriched hydrolyzed, Horus fermented placenta powder (HFPEP) from healthy, pathogen-free, swine placenta. Earlier studies demonstrated that HFPEP significantly improves physical fatigue, hepatic functions and repair of muscle fibers. We examined the broad safety of HFPEP in various toxicology models in Good Laboratory Practices-approved laboratories. The acute oral toxicity study was conducted in female Sprague-Dawley rats, and the acute oral LD50 was found to be greater than 5000 mg/kg body weight. Ames' bacterial reverse mutation assay was conducted to determine the ability of HFPEP to induce reverse mutation at selected histidine loci in five tester strains of Salmonella typhimurium viz. TA1535, TA1537, TA98, TA100 and TA102 in the presence and absence of a metabolic activation system (S9) at the doses of 50, 15, 4.5, 1.35 and 0.41 mg/ml. No mutagenic potential was observed. Mutagenic potential was also evaluated using in vivo micronucleus test, and no mutagenic potential of HFPEP was observed. Repeated dose 28-d oral toxicity study was performed in male and female rats with 14-d recovery period at the dose levels of 250, 500 or 1000 mg/kg. No abnormal clinical signs or toxicity were detected. No observed adverse effect level of HFPEP was found to be greater than 1000 mg/kg body weight. These studies affirm that HFPEP has broad spectrum safety for human consumption.
胎盘是一个重要器官,它连接发育中的胎儿,通过母体的血液供应实现营养摄取、抗体供应和气体交换。我们从健康、无病原体的猪胎盘中开发出一种新型、标准化、稳定、水溶性、富含肽的水解荷鲁斯发酵胎盘粉(HFPEP)。早期研究表明,HFPEP能显著改善身体疲劳、肝功能和肌肉纤维修复。我们在符合良好实验室规范的实验室中,在各种毒理学模型中检测了HFPEP的广泛安全性。在雌性斯普拉格-道利大鼠中进行了急性经口毒性研究,发现急性经口半数致死量大于5000毫克/千克体重。进行了艾姆斯氏细菌回复突变试验,以确定HFPEP在有和没有代谢活化系统(S9)的情况下,对鼠伤寒沙门氏菌五个测试菌株即TA1535、TA1537、TA98、TA100和TA102在选定组氨酸位点诱导回复突变的能力,剂量分别为50、15、4.5、1.35和0.41毫克/毫升。未观察到诱变潜力。还使用体内微核试验评估了诱变潜力,未观察到HFPEP的诱变潜力。在雄性和雌性大鼠中进行了重复剂量28天经口毒性研究,恢复期为14天,剂量水平为250、500或1000毫克/千克。未检测到异常临床体征或毒性。未观察到HFPEP的不良作用水平大于1000毫克/千克体重。这些研究证实,HFPEP对人类食用具有广泛的安全性。