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Dissociation Between Hormonal Counterregulatory Responses and Cerebral Glucose Metabolism During Hypoglycemia

Hypoglycemia is the most common complication of diabetes, causing morbidity and death. Recurrent hypoglycemia alters the cascade of physiological and behavioral responses that maintain euglycemia. The extent to which these responses are normally triggered by decreased whole-brain cerebral glucose me...

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Autores principales: Lee, John J., Khoury, Nadia, Shackleford, Angela M., Nelson, Suzanne, Herrera, Hector, Antenor-Dorsey, Jo Ann, Semenkovich, Katherine, Shimony, Joshua S., Powers, William J., Cryer, Philip E., Arbeláez, Ana María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697948/
https://www.ncbi.nlm.nih.gov/pubmed/28970283
http://dx.doi.org/10.2337/db17-0574
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author Lee, John J.
Khoury, Nadia
Shackleford, Angela M.
Nelson, Suzanne
Herrera, Hector
Antenor-Dorsey, Jo Ann
Semenkovich, Katherine
Shimony, Joshua S.
Powers, William J.
Cryer, Philip E.
Arbeláez, Ana María
author_facet Lee, John J.
Khoury, Nadia
Shackleford, Angela M.
Nelson, Suzanne
Herrera, Hector
Antenor-Dorsey, Jo Ann
Semenkovich, Katherine
Shimony, Joshua S.
Powers, William J.
Cryer, Philip E.
Arbeláez, Ana María
author_sort Lee, John J.
collection PubMed
description Hypoglycemia is the most common complication of diabetes, causing morbidity and death. Recurrent hypoglycemia alters the cascade of physiological and behavioral responses that maintain euglycemia. The extent to which these responses are normally triggered by decreased whole-brain cerebral glucose metabolism (CMR(glc)) has not been resolved by previous studies. We measured plasma counterregulatory hormonal responses and whole-brain CMR(glc) (along with blood-to-brain glucose transport rates and brain glucose concentrations) with 1-[(11)C]-d-glucose positron emission tomography during hyperinsulinemic glucose clamps at nominal plasma glucose concentrations of 90, 75, 60, and 45 mg/dL (5.0, 4.2, 3.3, and 2.5 mmol/L) in 18 healthy young adults. Clear evidence of hypoglycemic physiological counterregulation was first demonstrated between 75 mg/dL (4.2 mmol/L) and 60 mg/dL (3.3 mmol/L) with increases in both plasma epinephrine (P = 0.01) and glucagon (P = 0.01). In contrast, there was no statistically significant change in CMR(glc) (P = 1.0) between 75 mg/dL (4.2 mmol/L) and 60 mg/dL (3.3 mmol/L), whereas CMR(glc) significantly decreased (P = 0.02) between 60 mg/dL (3.3 mmol/L) and 45 mg/dL (2.5 mmol/L). Therefore, the increased epinephrine and glucagon secretion with declining plasma glucose concentrations is not in response to a decrease in whole-brain CMR(glc).
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spelling pubmed-56979482018-12-01 Dissociation Between Hormonal Counterregulatory Responses and Cerebral Glucose Metabolism During Hypoglycemia Lee, John J. Khoury, Nadia Shackleford, Angela M. Nelson, Suzanne Herrera, Hector Antenor-Dorsey, Jo Ann Semenkovich, Katherine Shimony, Joshua S. Powers, William J. Cryer, Philip E. Arbeláez, Ana María Diabetes Metabolism Hypoglycemia is the most common complication of diabetes, causing morbidity and death. Recurrent hypoglycemia alters the cascade of physiological and behavioral responses that maintain euglycemia. The extent to which these responses are normally triggered by decreased whole-brain cerebral glucose metabolism (CMR(glc)) has not been resolved by previous studies. We measured plasma counterregulatory hormonal responses and whole-brain CMR(glc) (along with blood-to-brain glucose transport rates and brain glucose concentrations) with 1-[(11)C]-d-glucose positron emission tomography during hyperinsulinemic glucose clamps at nominal plasma glucose concentrations of 90, 75, 60, and 45 mg/dL (5.0, 4.2, 3.3, and 2.5 mmol/L) in 18 healthy young adults. Clear evidence of hypoglycemic physiological counterregulation was first demonstrated between 75 mg/dL (4.2 mmol/L) and 60 mg/dL (3.3 mmol/L) with increases in both plasma epinephrine (P = 0.01) and glucagon (P = 0.01). In contrast, there was no statistically significant change in CMR(glc) (P = 1.0) between 75 mg/dL (4.2 mmol/L) and 60 mg/dL (3.3 mmol/L), whereas CMR(glc) significantly decreased (P = 0.02) between 60 mg/dL (3.3 mmol/L) and 45 mg/dL (2.5 mmol/L). Therefore, the increased epinephrine and glucagon secretion with declining plasma glucose concentrations is not in response to a decrease in whole-brain CMR(glc). American Diabetes Association 2017-12 2017-10-02 /pmc/articles/PMC5697948/ /pubmed/28970283 http://dx.doi.org/10.2337/db17-0574 Text en © 2017 by the American Diabetes Association. http://www.diabetesjournals.org/content/licenseReaders may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at http://www.diabetesjournals.org/content/license.
spellingShingle Metabolism
Lee, John J.
Khoury, Nadia
Shackleford, Angela M.
Nelson, Suzanne
Herrera, Hector
Antenor-Dorsey, Jo Ann
Semenkovich, Katherine
Shimony, Joshua S.
Powers, William J.
Cryer, Philip E.
Arbeláez, Ana María
Dissociation Between Hormonal Counterregulatory Responses and Cerebral Glucose Metabolism During Hypoglycemia
title Dissociation Between Hormonal Counterregulatory Responses and Cerebral Glucose Metabolism During Hypoglycemia
title_full Dissociation Between Hormonal Counterregulatory Responses and Cerebral Glucose Metabolism During Hypoglycemia
title_fullStr Dissociation Between Hormonal Counterregulatory Responses and Cerebral Glucose Metabolism During Hypoglycemia
title_full_unstemmed Dissociation Between Hormonal Counterregulatory Responses and Cerebral Glucose Metabolism During Hypoglycemia
title_short Dissociation Between Hormonal Counterregulatory Responses and Cerebral Glucose Metabolism During Hypoglycemia
title_sort dissociation between hormonal counterregulatory responses and cerebral glucose metabolism during hypoglycemia
topic Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697948/
https://www.ncbi.nlm.nih.gov/pubmed/28970283
http://dx.doi.org/10.2337/db17-0574
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