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      Ketogenic state improves testosterone serum levels—results from a systematic review and meta-analysis

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          Mechanisms, Pathophysiology, and Management of Obesity

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            Testosterone Therapy in Men With Hypogonadism: An Endocrine Society Clinical Practice Guideline

            To update the "Testosterone Therapy in Men With Androgen Deficiency Syndromes" guideline published in 2010.
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              The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders.

              Steroidogenesis entails processes by which cholesterol is converted to biologically active steroid hormones. Whereas most endocrine texts discuss adrenal, ovarian, testicular, placental, and other steroidogenic processes in a gland-specific fashion, steroidogenesis is better understood as a single process that is repeated in each gland with cell-type-specific variations on a single theme. Thus, understanding steroidogenesis is rooted in an understanding of the biochemistry of the various steroidogenic enzymes and cofactors and the genes that encode them. The first and rate-limiting step in steroidogenesis is the conversion of cholesterol to pregnenolone by a single enzyme, P450scc (CYP11A1), but this enzymatically complex step is subject to multiple regulatory mechanisms, yielding finely tuned quantitative regulation. Qualitative regulation determining the type of steroid to be produced is mediated by many enzymes and cofactors. Steroidogenic enzymes fall into two groups: cytochrome P450 enzymes and hydroxysteroid dehydrogenases. A cytochrome P450 may be either type 1 (in mitochondria) or type 2 (in endoplasmic reticulum), and a hydroxysteroid dehydrogenase may belong to either the aldo-keto reductase or short-chain dehydrogenase/reductase families. The activities of these enzymes are modulated by posttranslational modifications and by cofactors, especially electron-donating redox partners. The elucidation of the precise roles of these various enzymes and cofactors has been greatly facilitated by identifying the genetic bases of rare disorders of steroidogenesis. Some enzymes not principally involved in steroidogenesis may also catalyze extraglandular steroidogenesis, modulating the phenotype expected to result from some mutations. Understanding steroidogenesis is of fundamental importance to understanding disorders of sexual differentiation, reproduction, fertility, hypertension, obesity, and physiological homeostasis.
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                Author and article information

                Contributors
                Journal
                Endocrine
                Endocrine
                Springer Science and Business Media LLC
                1559-0100
                September 23 2022
                Article
                10.1007/s12020-022-03195-5
                36149528
                256d3273-b7fa-45b6-b21b-e5dfc3ca3f35
                © 2022

                https://www.springer.com/tdm

                https://www.springer.com/tdm

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