Department of Medical Education and Research, Kaohsiung Veterans General Hospital, Kaohsiung 81362, Taiwan.
J Nat Prod. 2012 Dec 28;75(12):2101-7. doi: 10.1021/np3005248. Epub 2012 Nov 19.
Diallyl sulfide (1), diallyl disulfide (2), and diallyl trisulfide (3), which are major organosulfur compounds of garlic (Allium sativum), are recognized as a group of potential chemopreventive compounds. In this study, the early signaling effects of 3 were examined on Madin-Darby canine kidney (MDCK) cells loaded with the Ca(2+)-sensitive dye fura-2. It was found that 3 caused an immediate and sustained increase of Ca(2+) in a concentration-dependent manner (EC(50) = 40 μM). Compound 3 also induced a Ca(2+) elevation when extracellular Ca(2+) was removed, but the magnitude was reduced by 45%. In Ca(2+)-free medium, the 3-induced Ca(2+) level was abolished by depleting stored Ca(2+) with 1 μM thapsigargin (an endoplasmic reticulum Ca(2+) pump inhibitor). Elevation of Ca(2+) caused by 3 in the Ca(2+)-containing medium was not affected by modulation of protein kinase C activity. The 3-induced Ca(2+) influx was inhibited by nifedipine and nicardipine (1 μM). U73122, an inhibitor of phospholipase C, abolished ATP (but not the 3-induced Ca(2+) level). These findings suggest that 3 induced a significant Ca(2+) elevation in MDCK renal tubular cells by stimulating both extracellular Ca(2+) influx and thapsigargin-sensitive intracellular Ca(2+) release via as yet unidentified mechanisms. Furthermore, the order of the allyl sulfide-induced Ca(2+) elevation and cell viability was 1 < 2 < 3. The differential effect of allyl sulfides on Ca(2+) signaling and cell death appears to correlate with the number of sulfur atoms in the structure of these allyl sulfides.
二烯丙基硫醚(1)、二烯丙基二硫醚(2)和二烯丙基三硫醚(3)是大蒜(Allium sativum)中的主要有机硫化合物,被认为是一组有潜在化学预防作用的化合物。在这项研究中,研究人员检测了 3 对负载 Ca(2+)敏感染料 fura-2 的 Madin-Darby 犬肾(MDCK)细胞的早期信号作用。结果发现,3 以浓度依赖的方式立即并持续增加 Ca(2+)(EC(50) = 40 μM)。当去除细胞外 Ca(2+)时,化合物 3 也会诱导 Ca(2+)的升高,但幅度降低了 45%。在无 Ca(2+)介质中,用 1 μM 他泊昔芬(内质网 Ca(2+)泵抑制剂)耗尽储存的 Ca(2+)可消除 3 诱导的 Ca(2+)水平。在含有 Ca(2+)的介质中,3 引起的 Ca(2+)升高不受蛋白激酶 C 活性调节的影响。硝苯地平和尼卡地平(1 μM)抑制 3 诱导的 Ca(2+)内流。磷脂酶 C 的抑制剂 U73122 消除了 ATP(但没有消除 3 诱导的 Ca(2+)水平)。这些发现表明,3 通过刺激细胞外 Ca(2+)内流和他泊昔芬敏感的细胞内 Ca(2+)释放,以未知的机制诱导 MDCK 肾小管细胞产生显著的 Ca(2+)升高。此外,烯丙基硫醚诱导的 Ca(2+)升高和细胞活力的顺序为 1 < 2 < 3。烯丙基硫醚对 Ca(2+)信号和细胞死亡的不同影响似乎与这些烯丙基硫醚结构中硫原子的数量有关。