[1]
|
Tallarida, R.J. (2000) Drug synergism and dose-effect data analysis. Chapman and Hall/CRC, Roca Raton.
doi:10.1201/9781420036107
|
[2]
|
Chou, T.-Ch. (2006) Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies. Pharmacological reviews, 58, 621-681. doi:10.1124/pr.58.3.10
|
[3]
|
Sergeev, P.V., Szymanowski, N.L. and Petrov, V.I. (1999) Receptors of physiologically active substances. 2nd Edition, “Seven Winds” Publishing House, Volgograd.
|
[4]
|
Stephenson, R.P. (1956) A modification of receptor theory. British Journal of Pharmacology, 11, 379-393.
|
[5]
|
Paton, W.D. (1961) A theory of drug action based on rate of drug-receptor combination. Proceedings of the Royal Society B: Biological Sciences, 154, 21-69.
doi:10.1098/rspb.1961.0020
|
[6]
|
Karlin, A. (1967) On the application of “a plausible model” of allosteric proteins to the receptor for acetylcholine. Journal of Theoretical Biology, 16, 306-320.
doi:10.1016/0022-5193(67)90011-2
|
[7]
|
Colquhoun, D. (1973) The relation between classical and cooperative models for drug action. In: Rang, H.P., Ed., Drug Receptors, Macmillan Press, London, 149-182.
|
[8]
|
Colquhoun, D. (1998) Binding, gating, affinity and efficacy. The interpretation of structure-activity relationships for agonists and of the effects of mutating receptors. British Journal of Pharmacology, 125, 923-948.
doi:10.1038/sj.bjp.0702164
|
[9]
|
De Lean, A., Stadel, J.M. and Lefkowitz, R.J. (1980) A ternary complex model explains the agonist-specific binding properties of the adenylate cyclase-coupled beta-adrenergic receptor. The Journal of Biological Chemistry, 255, 7108-7117.
|
[10]
|
Brugen, A. (1981) Conformational changes and drug action. FedProc, 40, 2723-2728.
|
[11]
|
Gero, A. (1983) Desensitization, two-state receptors and pharmacological parameters. Journal of Theoretical Biology, 103, 137-161.
doi:10.1016/0022-5193(83)90204-7
|
[12]
|
Urban, J.D, Clarke, W.P., Von Zastrow, M., Nichols, D.E., Kobilka, B., Weinstein, H., et al. (2007) Functional selectivity and classical concepts of quantitative pharmacology. The Journal of Pharmacology and Experimental Therapeutics, 320, 1-13. doi:10.1124/jpet.106.104463
|
[13]
|
Black, J.W., Leff, P., Shankley, N.P. and Wood, J. (2010) An operational model of pharmacological agonism: The effect of E/[A] curve shape on agonist dissociation constant estimation. British Journal of Pharmacology, 160, S54-S64. doi:10.1111/j.1476-5381.2010.00855.x
|
[14]
|
Kenakin, T. (2004) Principles: Receptor theory in pharmacology. Trends in Pharmacological Sciences, 25, 186-192. doi:10.1016/j.tips.2004.02.012
|
[15]
|
Strange, P.G. (2008) Agonist binding, agonist affinity and agonist efficacy at G protein-coupled receptors. British Journal of Pharmacology, 153, 1353-1363.
doi:10.1038/sj.bjp.0707672
|
[16]
|
Lambeth, J.D. (2007) Nox enzymes, ROS, and chronic disease: An example of antagonistic pleiotropy. Free Radical Biology & Medicine, 43, 332-347.
doi:10.1016/j.freeradbiomed.2007.03.027
|
[17]
|
Ito, M.K., Talbert, R.L. and Tsimikas, S. (2006) Statin-associated pleiotropy: Possible beneficial effects beyond cholesterol reduction. Pharmacotherapy, 26, 85S-97S.
doi:10.1592/phco.26.7part2.85S
|
[18]
|
Schroder, W., Tzschentke, T.M., Terlinden, R., De Vry, J., Jahnel, U., Christoph, T. and Tallarida, R.J. (2011) Synergistic interaction between the two mechanisms of action of tapentadol in analgesia. The Journal of Pharmacology and Experimental Therapeutics, 337, 312-320.
doi:10.1124/jpet.110.175042
|
[19]
|
Bizunok, N.A. (2013) Structural determinants of antioxidative activity of the phenols, diphenols and polyphenols at reactive oxygen species generated by macrophages in a different microenvironment circumstances. Military Medicine, 1, 84-94.
http://www.bsmu.by/files/vm/1-2013/24.pdf
|
[20]
|
Magocsi, M., Vizi, E.S., Selmeczy, Z., Brózik A. and Szelenyi, J. (2007) Multiple G-protein-coupling specificity of β-adrenoreceptor in macrophages. Immunology, 122, 503-513. doi:10.1111/j.1365-2567.2007.02658.x
|
[21]
|
García-García, E. and Rosales, C. (2002) Signal transduction during Fc receptor-mediated phagocytosis. Journal of Leukocyte Biology, 72, 1092-1108.
|
[22]
|
Luttrell, L.M. and Lefkowitz, R.J. (2002) The role of beta-arrestins in the termination and transduction of G-protein-coupled receptor signals. Journal of Cell Science, 115, 455-465.
|
[23]
|
Allanore, Y., Borderie, D., Perianin, A., Lemaréchal, H., Ekindjian, O.G. and Kahan, A. (2005) Nifedipine protects against overproduction of superoxide anion by monocytes from patients with systemic sclerosis. Arthritis Research & Therapy, 7, R93-R100. doi:10.1186/ar1457
|
[24]
|
Yurkova, I.L. (2010) Free radical fragmentation in the polar part of the lipids: A new path of destruction and the formation of biologically active compounds. Dissertation for the Degree of Doctor of Chemical Sciences, Belarusian State University, Minsk.
|
[25]
|
Tong Mac, I., Arroyo, M.C. and Weglicki, W.B. (1989) Inhibition of sarcolemmal carbon-centered free radical formation by propranolol. Circulation Research, 65, 1151-1156. doi:10.1186/ar1718
|