共查询到16条相似文献,搜索用时 62 毫秒
1.
2.
3.
4.
5.
6.
目的:对珍珠粉的食用安全性进行毒理学评价。方法:采用小鼠急性毒性试验、遗传毒性试验(Ames试验、小鼠骨髓细胞微核试验、小鼠精子畸形试验)和大鼠30 d喂养试验。结果:小鼠急性经口半数致死剂量(LD50)大于15 000 mg/(kg体重);Ames试验、小鼠骨髓细胞微核试验、小鼠精子畸形试验结果均为阴性;在30 d喂养试验中,大鼠的生长发育、血液学、生化、脏器重比及病理组织学未见与受试物相关的异常变化。结论:珍珠粉急性毒性属无毒级,无遗传毒性,珍珠粉30 d喂养实验未发现明显毒性反应,临床剂量安全。 相似文献
7.
目的对四年生鲜人参食用安全性进行毒理学评价。方法采用大鼠经FI急性毒性试验、遗传毒性试验(Ames试验、小鼠骨髓细咆微核试验、小鼠精子畸形试验)、大鼠30d喂养试验。结果雌、雄大鼠经口最大耐受剂龟(MTD)均大于18.6g/kg。3项遗传毒性试验结果均为阴性。在大鼠30d喂养试验中.8.0g/kg.4.0g/kg及2.0g/kg3个剂量组的实验动物均生长发育良好,体重、摄食量、饮水量、咀象、血液生化学、主要脏器系数及病理组织学相关指标均未见异常变化。结论四年生鲜人参属于实际无毒物,未见遗传毒性.长期服用是安全的。 相似文献
8.
目的 对五年生鲜人参的食用安全性进行毒理学评价.方法 采用小鼠、大鼠急性经口毒性试验、遗传毒性试验(Ames试验、小鼠骨髓细胞微核试验、小鼠精子畸形试验)、大鼠30d喂养试验.结果 雌、雄小鼠与大鼠经口最大耐受剂量(MTD)均大于19.2g/kg.bw.3项遗传毒性试验结果均为阴性,表明该受试物无致突变作用.在大鼠30d喂养试验中,实验动物均生长发育良好,体质量、摄食量、饮水量、血液学、血液生化学、脏器系数及病理组织学相关指标均未见异常变化.结论 五年生鲜人参属于实际无毒物,未见遗传毒性,长期服用安全. 相似文献
9.
10.
11.
目的评价元宝枫叶提取物的食用安全性。方法采用小鼠急性经口毒性试验、遗传毒性试验(小鼠骨髓细胞微核试验、小鼠精子畸变试验和Ames试验)及亚慢性毒性试验(90 d喂养试验)。结果元宝枫叶提取物对雌、雄性ICR小鼠经口最大耐受量均大于10 g/kg(本文剂量按每千克体质量所摄入受试物的克数计算),属实际无毒级;Ames试验、小鼠骨髓PCE微核试验和小鼠精子畸变试验结果均为阴性;在本实验剂量范围内摄入(1~2 g/kg),对实验大鼠的生长发育、食物利用率,血液系统、肝、肾功能、生殖系统,以及蛋白、脂肪、糖的代谢无明显影响。元宝枫叶提取物6 g/kg时对雄性实验大鼠体质量及进食量有影响(P〈0.05),6 g/kg剂量组在实验中期45 d的血液生物化学指标显示空腹血糖低于阴性对照组(P〈0.05)。结论元宝枫叶提取物在本实验条件下,未显示有急性毒性和遗传毒性;在1~2 g/kg剂量范围内未显示有亚慢性毒性。 相似文献
12.
13.
膦甲酸钠是一种抗病毒药物,其毒性与致突变性有关实验已进行研究。对小鼠LD50腹腔注射为1810mg/Kg;尾静脉注射为890mg/kg。对大鼠亚慢性毒性仅在高剂量组(900mg/kg/日)连续给药4周(总剂量达3083~5320mg/只)除体重增加稍为迟缓外,(但停药2周后即可恢复正常)。其余血常规;肝功能;肾功能等各项指标及病理切片检查,均未见明显的异常改变.致突变实验证明,无诱发小鼠骨髓细胞做核率升高.Ames试验阴性.以上实验结果表明膦甲酸钠是一种毒性较低的药物。 相似文献
14.
15.
目的:通过对啮齿动物进行急性和长期毒性实验研究,观察番石榴叶颗粒对大、小鼠的毒性反应,为临床安全用药提供实验依据.方法:急性毒性实验:用小鼠以口服给药,测定其最大耐受量(MTD),并推算出相当于临床人用量的倍数,以观察动物在短时间内出现的毒性反应.长期毒性实验:SD大鼠80只,雌雄各半,随机分成高(62.5g/kg)、中(25g/kg)、低(10g/kg)3个剂量组和空白对照组,连续灌胃给药1个月,观察大鼠一般状态、饮食、体重,于给药1个月后及停药2周后分别处死1/2的动物,取血测定血常规、血液生化指标,并取出主要脏器组织做病理组织学的检查,以观察连续用药对动物产生的毒性反应,以及停药后组织和功能损害的发展和恢复情况,了解毒性反应的可逆程度和可能出现的延迟性毒性反应.结果:急性毒性实验结果表明:番石榴叶颗粒的最大耐受量为562.5g/kg,相当于临床人用剂量的1125倍.长期毒性实验结果表明:大鼠体重逐周增长,各主要血象及血生化指标均未见异常,主要脏器病理组织学检查未见异常.结论:番石榴叶颗粒对大、小鼠无明显毒性反应,在临床推荐用量下口服连续给药安全可靠. 相似文献
16.
LI Shu Gang DING Yu Song NIU Qiang XU Shang Zhi PANG Li Juan MA Ru Lin JING Ming Xia FENG Gang Ling LIU Jia Ming GUO Shu Xia 《Biomedical and environmental sciences : BES》2015,(4):272-280
Objective To determine the ability of grape seed proanthocyanidin extract (GSPE) in alleviating arsenic-induced reproductive toxicity.
Methods Sixty male Kunming mice received the following treatments by gavage: normal saline solution (control); arsenic trioxide (ATO; 4 mg/kg); GSPE (400 mg/kg); ATO+GSPE (100 mg/kg);ATO+GSPE (200 mg/kg) and ATO+GSPE (400 mg/kg). Thereafter, the mice were sacrificed and weighed, and the testis was examined for pathological changes. Nuclear factor (erythroid-derived 2)-like 2 (Nrf2), heme oxygenase 1 (HO1), glutathione S-transferase (GST), NAD(P)H dehydrogenase, and quinone 1 (NQO1) expression in the testis was detected by real-time PCR. Superoxide dismutase (SOD), glutathione (GSH), total antioxidative capability (T-AOC), malondialdehyde (MDA), 8-hydroxydeoxyguanosine (8-OHdG), and reproductive indexes were analyzed.
Results ATO-treated mice showed a significantly decreased sperm count and testis somatic index and activity levels of SOD, GSH, and T-AOC than control group. Compared to the ATO-treated group, ATO+GSPE group showed recovery of the measured parameters. Mice treated with ATO+high-dose GSPE showed the highest level of mRNA expression of Nrf2, HO, NQO1, and GST.
Conclusion GSPE alleviates oxidative stress damage in mouse testis by activating Nrf2 signaling, thus counteracting arsenic-induced reproductive toxicity. 相似文献
Methods Sixty male Kunming mice received the following treatments by gavage: normal saline solution (control); arsenic trioxide (ATO; 4 mg/kg); GSPE (400 mg/kg); ATO+GSPE (100 mg/kg);ATO+GSPE (200 mg/kg) and ATO+GSPE (400 mg/kg). Thereafter, the mice were sacrificed and weighed, and the testis was examined for pathological changes. Nuclear factor (erythroid-derived 2)-like 2 (Nrf2), heme oxygenase 1 (HO1), glutathione S-transferase (GST), NAD(P)H dehydrogenase, and quinone 1 (NQO1) expression in the testis was detected by real-time PCR. Superoxide dismutase (SOD), glutathione (GSH), total antioxidative capability (T-AOC), malondialdehyde (MDA), 8-hydroxydeoxyguanosine (8-OHdG), and reproductive indexes were analyzed.
Results ATO-treated mice showed a significantly decreased sperm count and testis somatic index and activity levels of SOD, GSH, and T-AOC than control group. Compared to the ATO-treated group, ATO+GSPE group showed recovery of the measured parameters. Mice treated with ATO+high-dose GSPE showed the highest level of mRNA expression of Nrf2, HO, NQO1, and GST.
Conclusion GSPE alleviates oxidative stress damage in mouse testis by activating Nrf2 signaling, thus counteracting arsenic-induced reproductive toxicity. 相似文献