The Hill equation and the origin of quantitative pharmacology

被引:257
作者
Gesztelyi, Rudolf [1 ]
Zsuga, Judit [2 ]
Kemeny-Beke, Adam [3 ]
Varga, Balazs [1 ]
Juhasz, Bela [1 ]
Tosaki, Arpad [1 ]
机构
[1] Univ Debrecen, Dept Pharmacol, Fac Pharm, H-4012 Debrecen, Hungary
[2] Univ Debrecen, Dept Neurol, Fac Med, H-4012 Debrecen, Hungary
[3] Univ Debrecen, Dept Ophthalmol, Fac Med, H-4012 Debrecen, Hungary
基金
匈牙利科学研究基金会;
关键词
CONCENTRATION-EFFECT CURVES; DRUG-RECEPTOR INTERACTIONS; MODELS; AGONISM; CHOLINE; TERMS;
D O I
10.1007/s00407-012-0098-5
中图分类号
N09 [自然科学史]; B [哲学、宗教];
学科分类号
01 ; 0101 ; 010108 ; 060207 ; 060305 ; 0712 ;
摘要
This review addresses the 100-year-old Hill equation (published in January 22, 1910), the first formula relating the result of a reversible association (e.g., concentration of a complex, magnitude of an effect) to the variable concentration of one of the associating substances (the other being present in a constant and relatively low concentration). In addition, the Hill equation was the first (and is the simplest) quantitative receptor model in pharmacology. Although the Hill equation is an empirical receptor model (its parameters have only physico-chemical meaning for a simple ligand binding reaction), it requires only minor a priori knowledge about the mechanism of action for the investigated agonist to reliably fit concentration-response curve data and to yield useful results (in contrast to most of the advanced receptor models). Thus, the Hill equation has remained an important tool for physiological and pharmacological investigations including drug discovery, moreover it serves as a theoretical basis for the development of new pharmacological models.
引用
收藏
页码:427 / 438
页数:12
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