The behaviour of some antihypertension drugs on human serum paraoxonase-1: an important protector enzyme against atherosclerosis

被引:90
作者
Demir, Yeliz [1 ,2 ]
机构
[1] Ataturk Univ, Fac Sci, Dept Chem, Erzurum, Turkey
[2] Ardahan Univ, Nihat Delibalta Gole Vocat High Sch, Dept Pharm Serv, Ardahan, Turkey
关键词
enzyme purification; hypertension; inhibition; paraoxonase; beta-adrenoceptor blocking drugs; ANHYDRASE INHIBITORY PROPERTIES; IN-VITRO; PON1; BETA-BLOCKERS; ANTIOXIDANT; PURIFICATION; HYDROCHLORIDE; ASSOCIATION; PROTEINS; PLASMA;
D O I
10.1111/jphp.13144
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives Paraoxonase-1 (PON1) enzyme is related to high-density lipoprotein (HDL), which is calcium dependent. It has essential roles such as protecting LDL against oxidation and detoxification of highly toxic substances. It is a significant risk to reduce the levels of this enzyme in patients with diabetes mellitus, cardiovascular diseases, hyperthyroidism and chronic renal failure. Methods Here, it was reported that the purification of human serum PON1 using straightforward methods and determination of the interactions between some antihypertension drugs and the enzyme. Key finding It was found that these drugs exhibit potential inhibitor properties for human serum PON1 with IC50 values in the range of 131.40-369.40 mu m and K-i values in the range of 56.24 +/- 6.75-286.74 +/- 28.28 mu m. These drugs showed different inhibition mechanisms. It was determined that midodrine and nadolol were exhibited competitive inhibition, but atenolol and pindolol were exhibited non-competitive inhibition. Conclusion Usage of these drugs would be hazardous in some cases.
引用
收藏
页码:1576 / 1583
页数:8
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