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Infusion of N‐acetyl cysteine during hypoglycaemia in humans does not preserve the counterregulatory response to subsequent hypoglycaemia

AIM: Administration of N‐acetyl cysteine (NAC) during hypoglycaemia will preserve the counterregulatory response to subsequent hypoglycaemia in healthy humans. METHODS: This was a randomized double‐blind cross over study where humans were given either a 60‐minute infusion of NAC (150 mg/kg) followed...

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Autores principales: Moheet, Amir, Kumar, Anjali, Zhang, Yuan, Eberly, Lynn, Coles, Lisa D., Seaquist, Elizabeth R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375074/
https://www.ncbi.nlm.nih.gov/pubmed/32704565
http://dx.doi.org/10.1002/edm2.144
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author Moheet, Amir
Kumar, Anjali
Zhang, Yuan
Eberly, Lynn
Coles, Lisa D.
Seaquist, Elizabeth R.
author_facet Moheet, Amir
Kumar, Anjali
Zhang, Yuan
Eberly, Lynn
Coles, Lisa D.
Seaquist, Elizabeth R.
author_sort Moheet, Amir
collection PubMed
description AIM: Administration of N‐acetyl cysteine (NAC) during hypoglycaemia will preserve the counterregulatory response to subsequent hypoglycaemia in healthy humans. METHODS: This was a randomized double‐blind cross over study where humans were given either a 60‐minute infusion of NAC (150 mg/kg) followed by a 4‐hour infusion of NAC (50 mg/kg) or saline starting 30 minutes before the initiation of a 2‐hour hypoglycaemic (HG) clamp at 8 am. After rest at euglycaemia for ~2 hours, subjects were exposed to a 2nd HG clamp at 2 pm and discharged home in euglycaemia. They returned the following day for a 3rd HG clamp at 8 am. RESULTS: Twenty‐two subjects were enrolled. Eighteen subjects completed the entire protocol. The epinephrine response during clamp 3 (171 ± 247 pg/mL) following clamp 1 NAC infusion was lower than the response during the clamp 1 NAC infusion (538 ± 392 pg/mL) (clamp 3 to clamp 1 NAC: P = .0013). The symptom response during clamp 3 (7 ± 5) following clamp 1 NAC infusion was lower than the response during the clamp 1 NAC infusion (16 ± 10) (clamp 3 to clamp 1 NAC: P = .0003). Nine subjects experienced rash, pruritus or nausea during NAC infusion. CONCLUSION: We found no difference in the hormone and symptom response to experimental hypoglycaemia measured in subjects who were administered NAC as opposed to saline the day before. This observation suggests that further development of NAC as a therapy for impaired awareness of hypoglycaemia in patients with diabetes may be unwarranted.
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spelling pubmed-73750742020-07-22 Infusion of N‐acetyl cysteine during hypoglycaemia in humans does not preserve the counterregulatory response to subsequent hypoglycaemia Moheet, Amir Kumar, Anjali Zhang, Yuan Eberly, Lynn Coles, Lisa D. Seaquist, Elizabeth R. Endocrinol Diabetes Metab Original Research Articles AIM: Administration of N‐acetyl cysteine (NAC) during hypoglycaemia will preserve the counterregulatory response to subsequent hypoglycaemia in healthy humans. METHODS: This was a randomized double‐blind cross over study where humans were given either a 60‐minute infusion of NAC (150 mg/kg) followed by a 4‐hour infusion of NAC (50 mg/kg) or saline starting 30 minutes before the initiation of a 2‐hour hypoglycaemic (HG) clamp at 8 am. After rest at euglycaemia for ~2 hours, subjects were exposed to a 2nd HG clamp at 2 pm and discharged home in euglycaemia. They returned the following day for a 3rd HG clamp at 8 am. RESULTS: Twenty‐two subjects were enrolled. Eighteen subjects completed the entire protocol. The epinephrine response during clamp 3 (171 ± 247 pg/mL) following clamp 1 NAC infusion was lower than the response during the clamp 1 NAC infusion (538 ± 392 pg/mL) (clamp 3 to clamp 1 NAC: P = .0013). The symptom response during clamp 3 (7 ± 5) following clamp 1 NAC infusion was lower than the response during the clamp 1 NAC infusion (16 ± 10) (clamp 3 to clamp 1 NAC: P = .0003). Nine subjects experienced rash, pruritus or nausea during NAC infusion. CONCLUSION: We found no difference in the hormone and symptom response to experimental hypoglycaemia measured in subjects who were administered NAC as opposed to saline the day before. This observation suggests that further development of NAC as a therapy for impaired awareness of hypoglycaemia in patients with diabetes may be unwarranted. John Wiley and Sons Inc. 2020-05-15 /pmc/articles/PMC7375074/ /pubmed/32704565 http://dx.doi.org/10.1002/edm2.144 Text en © 2020 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Articles
Moheet, Amir
Kumar, Anjali
Zhang, Yuan
Eberly, Lynn
Coles, Lisa D.
Seaquist, Elizabeth R.
Infusion of N‐acetyl cysteine during hypoglycaemia in humans does not preserve the counterregulatory response to subsequent hypoglycaemia
title Infusion of N‐acetyl cysteine during hypoglycaemia in humans does not preserve the counterregulatory response to subsequent hypoglycaemia
title_full Infusion of N‐acetyl cysteine during hypoglycaemia in humans does not preserve the counterregulatory response to subsequent hypoglycaemia
title_fullStr Infusion of N‐acetyl cysteine during hypoglycaemia in humans does not preserve the counterregulatory response to subsequent hypoglycaemia
title_full_unstemmed Infusion of N‐acetyl cysteine during hypoglycaemia in humans does not preserve the counterregulatory response to subsequent hypoglycaemia
title_short Infusion of N‐acetyl cysteine during hypoglycaemia in humans does not preserve the counterregulatory response to subsequent hypoglycaemia
title_sort infusion of n‐acetyl cysteine during hypoglycaemia in humans does not preserve the counterregulatory response to subsequent hypoglycaemia
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375074/
https://www.ncbi.nlm.nih.gov/pubmed/32704565
http://dx.doi.org/10.1002/edm2.144
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