The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.
Regulation of gluconeogenesis by glucocorticoids.
Abstract
1. Regulation of gluconeogenic substrate supply and modulation of the gluconeogenic pathway in the liver are both important in the control of gluconeogenesis by glucocorticoids. 2. Adrenal deficiency decreases the release of gluconeogenic and other amino acids from skeletal muscle during starvation. The effect is reversed by glucocorticoid replacement. The changes in amino acid release are accompanied by similar alterations in tissue amino acid levels and are not explained by alterations in net protein breakdown. Glucocorticoids do not alter protein catabolism and cause a small inhibition of protein synthesis. The biochemical alterations underlying the changes in amino acid metabolism induced by these steroids remain to be elucidated. Glucocorticoids may also regulate the supply of gluconeogenic substrates through permissive effects on the lipolytic action of catecholamines and other hormones in adipose tissue and on the glycogenolytic action of catecholamines on skeletal muscle. 3. Glucocorticoids are required for the increases in gluconeogenesis in starvation and diabetes. Part of their action is exerted directly on the liver and appears to involve modulation of P-enlopyruvate carboxykinase levels. Glucocorticoids increase the synthesis of this enzyme apparently through effects at the level of transcription. 4. Glucocorticoids exert permissive effects on the stimulation of gluconeogenesis in the liver by glucagon and epinephrine. The steroids are not required for cAMP generation or protein kinase activation by these hormones, but appear to act by maintaining the responsiveness of certain enzymes to the effects of the cAMP and alpha-adrenergic systems. It is proposed that this involves the maintenance of a normal intracellular ionic environment.
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“Glucocorticoids can exacerbate hyperglycemia by increasing hepatic gluconeogenesis (by inducing expression of G6Pase and Pepck) (46)”
From Leptin Activates a Novel CNS Mechanism for Insulin-Independent Normalization of Severe Diabetic Hyperglycemia (2011) · cites this paper as [46]
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“Increased substrates for gluconeogenesis are primarily amino acids released from muscle and other peripheral tissues, and glycerol released from adipose tissue sensitized permissively by GCs to lipolysis by GH and catecholamines (419, 420).”
BackgroundRegulation of glucose homeostasis by glucocorticoids
Kuo, T., McQueen, A., Chen, T.-C., & Wang, J.-C. (2015) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-2895-8_5 · Cited by 723
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“…travel throughout the body, exerting a multitude of effects in the periphery including glycogen breakdown and gluconeogenesis (Coderre et al., 1991; Exton, 1979; Munck et al., 1984; for detailed reviews of brain circuits regulating glucose homeostasis see Schwartz et al., 2000; Seeley and Woods,…”
BackgroundAquaglyceroporin AQP9: Solute permeation and metabolic control of expression in liver
Carbrey, J. M., Gorelick-Feldman, D. A., Kozono, D., Prætorius, J., Nielsen, S., & Agre, P. C. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0437994100 · Cited by 306
Adrenal Corticosteroid Biosynthesis, Metabolism, and Action
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“Hepatic glucose output increases through the activation of key enzymes involved in gluconeogenesis, principally glucose-6-phosphatase and phosphoenolpyruvate kinase (PEPCK) [67].”
Background
Metadata
- Authors
- Exton, J. H.
- Corresponding author
- Exton, J. H.
- Venue
- Monographs on endocrinology
- Publisher
- Springer Berlin Heidelberg
- Published
- 1979
- Volume
- 12
- Pages
- 535-546
- ISSN
- 0077-1015 (ISSN-L)
- OpenAlex
- W2407810808
- Cited by
- 130
- References
- 46
- Citations by year
- 2026: 5 · 2025: 4 · 2024: 6 · 2023: 10 · 2022: 8 · 2021: 3 · 2020: 10 · 2019: 4 · 2018: 2 · 2017: 4 · 2016: 5 · 2015: 4 · 2014: 1 · 2013: 3 · 2012: 4
- FWCI
- 2.39
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- Monographs on endocrinology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Estrogen and related hormone effects
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Keywords
- gluconeogenesis, glucocorticoids, starvation, adrenal insufficiency, glucocorticoid replacement therapy, protein synthesis, lipolysis, catecholamines, glycogenolysis, transcriptional regulation, glucagon, epinephrine, cAMP signaling, alpha-adrenergic receptors, diabetes mellitus
- MeSH terms
- Adrenalectomy, Animals, Diabetes Mellitus, Experimental, Epinephrine, Glucagon, Glucocorticoids, Gluconeogenesis, Hydrocortisone, Liver, Rats
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