The Conjugated Double Bond of Coniferyl Aldehyde Is Essential for Heat Shock Factor 1 Mediated Cytotoprotection.
Seul-Ki ChoiGil-Im MunEun ChoiSeo-Young KimYoungjoo KwonYounghwa NaYun-Sil LeePublished in: Journal of natural products (2017)
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.
Keyphrases
- heat shock
- heat stress
- induced apoptosis
- heat shock protein
- oxidative stress
- bone marrow
- cell cycle arrest
- mesenchymal stem cells
- endoplasmic reticulum stress
- cell death
- photodynamic therapy
- signaling pathway
- radiation induced
- adipose tissue
- molecular docking
- metabolic syndrome
- skeletal muscle
- rectal cancer
- electron transfer