Nagle Dale G, Zhou Yu-Dong
Department of Pharmacognosy, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS 38677-1848, USA.
Curr Pharm Des. 2006;12(21):2673-88. doi: 10.2174/138161206777698783.
Hypoxia-inducible factor-1 (HIF-1) is a key mediator of oxygen homeostasis that was first identified as a transcription factor that is induced and activated by decreased oxygen tension. Upon activation, HIF-1 upregulates the transcription of genes that promote adaptation and survival under hypoxic conditions. HIF-1 is a heterodimer composed of an oxygen-regulated subunit known as HIF-1alpha and a constitutively expressed HIF-1beta subunit. In general, the availability and activity of the HIF-1alpha subunit determines the activity of HIF-1. Subsequent studies have revealed that HIF-1 is also activated by environmental and physiological stimuli that range from iron chelators to hormones. Preclinical studies suggest that HIF-1 activation may be a valuable therapeutic approach to treat tissue ischemia and other ischemia/hypoxia-related disorders. The focus of this review is natural product-derived small molecule HIF-1 activators. Natural products, relatively low molecular weight organic compounds produced by plants, animals, and microbes, have been and continue to be a major source of new drugs and molecular probes. The majority of known natural product-derived HIF-1 activators were discovered through the pharmacological evaluation of specifically selected individual compounds. On the other hand, the combination of natural products chemistry with appropriate high-throughput screening bioassays may yield novel natural product-derived HIF-1 activators. Potent natural product-derived HIF-1 activators that exhibit a low level of toxicity and side effects hold promise as new treatment options for diseases such as myocardial and peripheral ischemia, and as chemopreventative agents that could be used to reduce the level of ischemia/reperfusion injury following heart attack and stroke.
缺氧诱导因子-1(HIF-1)是氧稳态的关键调节因子,最初被鉴定为一种受氧张力降低诱导并激活的转录因子。激活后,HIF-1上调在缺氧条件下促进适应和存活的基因转录。HIF-1是一种异源二聚体,由一个称为HIF-1α的氧调节亚基和一个组成型表达的HIF-1β亚基组成。一般来说,HIF-1α亚基的可用性和活性决定了HIF-1的活性。随后的研究表明,HIF-1也可被从铁螯合剂到激素等各种环境和生理刺激激活。临床前研究表明,激活HIF-1可能是治疗组织缺血和其他缺血/缺氧相关疾病的一种有价值的治疗方法。本综述的重点是天然产物衍生的小分子HIF-1激活剂。天然产物是由植物、动物和微生物产生的相对低分子量的有机化合物,一直是并将继续是新药和分子探针的主要来源。大多数已知的天然产物衍生的HIF-1激活剂是通过对特定选择的单个化合物进行药理评估而发现的。另一方面,天然产物化学与适当的高通量筛选生物测定相结合可能会产生新型的天然产物衍生的HIF-1激活剂。具有低毒性和副作用的强效天然产物衍生的HIF-1激活剂有望成为治疗心肌和外周缺血等疾病的新选择,以及作为可用于降低心脏病发作和中风后缺血/再灌注损伤水平的化学预防剂。