The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Catecholamines: Znediator of the Hypermetabolic Response to Thermal Injury
Open accessAbstract
Hypermetabolism characterizes the metabolic response to thermal injury and the extent of energy production is positively related to the rate of urinary catecholamine excretion. Alpha and beta adrenergic blockade decreased metabolism from 69.6 +/- 5.3 Kcal/m(2)/hr to 57.4 +/- 5.2 (p < 0.01), and infusion of 6 microgm epinephrine/minute in normal man significantly increased metabolic rate. Twenty noninfected burned adults with a mean burn size of 45% total body surface (range 7-84%) and four normal controls were studied in an environmental chamber at two or more temperatures between 19 and 33 C with vapor pressure constant at 11.88 mm Hg. All burn patients were hypermetabolic at all temperatures studied and their core and mean skin temperatures were significantly elevated above control values. Between 25 and 33 C ambient, metabolism was unchanged in controls and burns of less than 40% total body surface (48.9 +/- 4.6 Kcal/m(2)/hr vs. 48.9 +/- 4.5), but metabolic rate decreased in larger burns in the warmer environment (72.0 +/- 1.9 vs. 65.8 +/- 1.7, p < 0.001). At 21 C, metabolism and catecholamines increased, except in four nonsurvivors who became hypothermic with decreased catechol elaboration. Metabolic rate in ten patients with bacteremia was below predicted levels while catecholamines were markedly elevated suggesting interference with tissue uptake of the neurohormonal transmitters. Feeding burn patients or administering glucose and insulin improved nitrogen retention and altered substrate flow but did not significantly reduce urinary catecholamines or metabolic rate. Burned patients are internally warm, not externally cold, and catecholamines appear to mediate their increased heat production. Hypermetabolism may be modified by ambient temperature, infection, and pharmacologic means. Alterations in hypothalamic function due to injury, resulting in increased catecholamine elaboration, would explain the metabolic response to thermal injury.
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INITIAL METABOLIC AND HORMONAL RESPONSE TO ACUTE MYOCARDIAL INFARCTION
Vetter, N. J., Adams, W., Strange, R. C., & Oliver, M. F. (1974) · The Lancet · doi:10.1016/s0140-6736(74)92595-1 · Cited by 207
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Persistence of muscle catabolism after severe burn
Hart, D. W., Wolf, S. E., Mlcak, R., Chinkes, D. L., Ramzy, P. I., Obeng, M. K., Ferrando, A. A., Wolfe, R. R., & Herndon, D. N. (2000) · Surgery · doi:10.1067/msy.2000.108059 · Cited by 543
Support of the metabolic response to burn injury
Herndon, D. N., & Tompkins, R. G. (2004) · The Lancet · doi:10.1016/s0140-6736(04)16360-5 · Cited by 532
Effect of Severe Burn Injury on Substrate Cycling by Glucose and Fatty Acids
Wolfe, R. R., Herndon, D. N., Jahoor, F., Miyoshi, H., & Wolfe, M. (1987) · New England Journal of Medicine · doi:10.1056/nejm198708133170702 · Cited by 467
The Surgically Induced Stress Response
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Metadata
- Authors
- WILMORE, D. W., LONG, J. M., MASON, A. D., SKREEN, R. W., & PRUITT, B. A.
- Venue
- Annals of Surgery
- Published
- 1974-10
- Volume
- 180
- Issue
- 4
- Pages
- 653-669
- ISSN
- 0003-4932 (ISSN-L)
- OpenAlex
- W1967775253
- Cited by
- 753
- References
- 1
- FWCI
- 18.02
- Type
- journal article
- Language
- en
- Open access
- green
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- WILMORE, D. W., LONG, J. M., MASON, A. D., SKREEN, R. W., & PRUITT, B. A. (1974). Catecholamines: Znediator of the Hypermetabolic Response to Thermal Injury. Annals of Surgery. https://doi.org/10.1097/00000658-197410000-00031
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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