Choi Seul-Ki, Mun Gil-Im, Choi Eun, Kim Seo-Young, Kwon Youngjoo, Na Younghwa, Lee Yun-Sil
Graduate School of Pharmaceutical Sciences, Ewha Womans University , Seoul 120-750, Korea.
College of Pharmacy, CHA University , Pocheon 487-010, Korea.
J Nat Prod. 2017 Aug 25;80(8):2379-2383. doi: 10.1021/acs.jnatprod.7b00126. Epub 2017 Jul 24.
Coniferyl aldehyde (1) is previously reported as a potent inducer of heat shock factor 1 (HSF1). Here, we further examined the active pharmacophore of 1 for activation of HSF1 using the derivatives coniferyl alcohol (2), 4-hydroxy-3-methoxyphenylpropanal (3), and 4-hydroxy-3-methoxyphenylpropanol (4). Both 1 and 2 resulted in increased survival days after a lethal radiation (IR) dose. The decrease in bone marrow (BM) cellularity and Ki67-positive BM cells by IR was also significantly restored by 1 or 2 in mice. These results suggested that the vinyl moiety of 1 and 2 is necessary for inducing HSF1, which may be useful for developing small molecules for cytoprotection of normal cells against damage by cytotoxic drugs and radiation.
松柏醛(1)先前被报道为热休克因子1(HSF1)的有效诱导剂。在此,我们使用松柏醇(2)、4-羟基-3-甲氧基苯丙醛(3)和4-羟基-3-甲氧基苯丙醇(4)衍生物进一步研究了1激活HSF1的活性药效团。1和2均导致致死性辐射(IR)剂量后的存活天数增加。在小鼠中,IR导致的骨髓(BM)细胞数量和Ki67阳性BM细胞的减少也被1或2显著恢复。这些结果表明,1和2的乙烯基部分对于诱导HSF1是必需的,这可能有助于开发小分子以保护正常细胞免受细胞毒性药物和辐射的损伤。