Shakibaie Mojtaba, Abharian Azam, Forootanfar Hamid, Ameri Atefeh, Jafari Mandana, Reza Rahimi Hamid
Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Kerman University of Medical Sciences, Kerman, Iran.
Department of Toxicology and Pharmacology, Faculty of Pharmacy, Kerman University of Medical Sciences, Kerman, Iran.
IET Nanobiotechnol. 2018 Dec;12(8):1144-1149. doi: 10.1049/iet-nbt.2018.5137.
The authors evaluated the cytotoxicity underlying mechanisms of biogenic tellurium (Te) nanorods (NRs) produced by the strain Te on the PC12 cell line. The half-maximal inhibitory concentration (IC) value was estimated at 5.05 ± 0.07 ng/ml for biogenic Te NRs and 2.44 ± 0.38 ng/ml for KTeO, respectively. The viability of PC12 was inhibited concentration dependent at doses of 1, 2.5, 5, 10, and 20 ng/ml. Te NRs principally induced late apoptosis or necrosis at IC concentration, without effect on caspase-3 activities. Furthermore, Te NRs reduced glutathione and enhanced malondialdehyde levels, and also reduced superoxide dismutase and catalase activities. These findings revealed that biogenic Te NRs were less toxic than KTeO. Additionally, they induced cytotoxity towards the PC12 cell line through the activation of late apoptosis independent of the caspase pathway, and may also enhance oxidative stress in the nervous system.
作者评估了菌株产生的生物源碲(Te)纳米棒(NRs)对PC12细胞系的细胞毒性潜在机制。生物源Te NRs的半数抑制浓度(IC)值估计为5.05±0.07 ng/ml,KTeO的IC值为2.44±0.38 ng/ml。在1、2.5、5、10和20 ng/ml剂量下,PC12的活力受到浓度依赖性抑制。Te NRs在IC浓度下主要诱导晚期凋亡或坏死,对caspase-3活性无影响。此外,Te NRs降低了谷胱甘肽水平,提高了丙二醛水平,还降低了超氧化物歧化酶和过氧化氢酶活性。这些发现表明,生物源Te NRs的毒性低于KTeO。此外,它们通过激活独立于caspase途径的晚期凋亡诱导对PC12细胞系的细胞毒性,还可能增强神经系统中的氧化应激。