Zhang Fang, Zhang Yongchun, Wang Kaiming, Zhu Xiaosong, Lin Guimei, Zhao Zhongxi, Li Shanzhong, Cai Jianhua, Cao Jimin
School of Pharmaceutical Sciences, Shandong University, 44 West Wenhua Road, Jinan 250012, PR China.
School of Pharmaceutical Sciences, Shandong University, 44 West Wenhua Road, Jinan 250012, PR China; School of Chemistry and Pharmaceutical Engineering, Qilu University of Technology, Daxue Road, Western University Science Park, Jinan, Shandong 250353, PR China.
Int Immunopharmacol. 2015 Dec;29(2):326-333. doi: 10.1016/j.intimp.2015.10.033. Epub 2015 Nov 6.
Diallyl trisulfide (DATS) is a garlic organosulfide that may have a therapeutic potential in the treatment of some diseases. We sought to determine whether DATS could inhibit naphthalene-induced oxidative injury and the production of inflammatory responses in vitro and in vivo. A549 cells were either pre-treated (PreTx, prevention) or concurrently treated (CoTx, treatment) with 20μM naphthalene and either 5 or 10μM DATS. PreTx and CoTx showed the prevention and the treatment potential of DATS to inhibit the generation of naphthalene-induced reactive oxygen species (ROS) in the A549 cells. DATS showed antioxidative activity by elevating the SOD activities in the low dose groups. The mechanistic study showed that the DATS-mediated inhibition of naphthalene-induced oxidative injury and the production of inflammatory responses (i.e., TNF-α, IL-6, and IL-8) were attributed to inhibiting the activity of nuclear factor-kappa B (NF-κB). In addition, DATS inhibited the production of serum nitric oxide NO and myeloperoxidase (MPO) in the lungs of Kunming mice. The histological analysis results indicate that DATS inhibited the naphthalene-induced lung damage, which is consistent with the in vitro study results. The in vivo and in vitro results suggest that DATS may be an effective attenuator of naphthalene-induced lung damage.
二烯丙基三硫化物(DATS)是一种大蒜有机硫化物,在某些疾病的治疗中可能具有治疗潜力。我们试图确定DATS在体外和体内是否能抑制萘诱导的氧化损伤和炎症反应的产生。A549细胞用20μM萘和5或10μM DATS进行预处理(PreTx,预防)或同时处理(CoTx,治疗)。PreTx和CoTx显示出DATS在抑制A549细胞中萘诱导的活性氧(ROS)生成方面的预防和治疗潜力。DATS通过提高低剂量组的超氧化物歧化酶(SOD)活性表现出抗氧化活性。机制研究表明,DATS介导的对萘诱导的氧化损伤和炎症反应(即肿瘤坏死因子-α、白细胞介素-6和白细胞介素-8)产生的抑制作用归因于抑制核因子-κB(NF-κB)的活性。此外,DATS抑制昆明小鼠肺组织中血清一氧化氮(NO)和髓过氧化物酶(MPO)的产生。组织学分析结果表明,DATS抑制了萘诱导的肺损伤,这与体外研究结果一致。体内和体外结果表明,DATS可能是萘诱导的肺损伤的有效减轻剂。