Glucocorticoid hormones directly or indirectly control virtually all metabolic and physiological processes. Glucocorticoids are also shown to act on a multitude of genes, enzyme systems, and proinflammatory factors, but for these hormones there is no representative index of action on metabolism similar to glucose content in blood for insulin. The absence of such an index prevents the assessment of tissue provision with these hormones under various conditions and seems to be an essential cause of complications associated with the clinical use of glucocorticoid preparations. Considering specific features of tyrosine metabolism and data obtained experimentally and on a clinical model (adrenalectomy in rats and substitution therapy in endocrine disease), blood content of this amino acid seems promising as such an index. Based on comparing results of glucocorticoid treatment in patients with systemic lupus erythematosus with changes in their blood tyrosine contents, the pharmacological effect of glucocorticoid preparations is suggested to be mainly due to compensating a relative shortage of these hormones.
Glucocorticoid (GC) preparations are used in medicine for about 70 years as the most powerful anti-inflammatory drugs also possessing immunosuppressive, anti-allergic and antitoxic properties. However, application of these unique preparations is associated with nearly inevitable serious adverse effects and a difficulty of their withdrawal. It is very important that the adverse effects are caused not by toxic action of GC preparations but by their hormonal nature. Glucocorticoid hormones directly or indirectly control virtually all metabolic and physiological processes in the body. However, for these virtually omnipresent and vitally important hormones there is no representative specific index of action similar to blood content of glucose for insulin. The present paper considers specific features of tyrosine metabolism that allows us to consider changes in blood tyrosine content as manifestation of regulatory action of GCs. Changes in blood tyrosine content were compared with using GC preparations in two typical cases: in systemic lupus erythematosus and in congenital adrenal virilizing dysfunction in children. Blood tyrosine behavior was also considered in rats after adrenalectomy and on injecting them with hydrocortisone. Based on these observations, it is proposed to use blood content of tyrosine as a laboratory test for reasonable prescribing GC preparations and monitoring their dose. Blood tyrosine behavior in comparison with adrenocortical response is also considered in influenza.
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