Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Tytuł pozycji:

Repeated exposure to sucrose for procedural pain in mouse pups leads to long-term widespread brain alterations.

Tytuł:
Repeated exposure to sucrose for procedural pain in mouse pups leads to long-term widespread brain alterations.
Autorzy:
Tremblay S; Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.; BC Children's Hospital Research Institute, Vancouver, BC, Canada.; Centre for Molecular Medicine and Therapeutics, Vancouver, BC, Canada.
Ranger M; Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.; BC Children's Hospital Research Institute, Vancouver, BC, Canada.; Department of Psychiatry, Developmental Neuroscience Division, Nurture Science Program, Columbia University, New York, NY, USA.
Chau CMY; Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.; BC Children's Hospital Research Institute, Vancouver, BC, Canada.
Ellegood J; Mouse Imaging Centre, Hospital for Sick Children, Toronto, ON, Canada.
Lerch JP; Mouse Imaging Centre, Hospital for Sick Children, Toronto, ON, Canada.; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Holsti L; BC Children's Hospital Research Institute, Vancouver, BC, Canada.; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Goldowitz D; BC Children's Hospital Research Institute, Vancouver, BC, Canada.; Centre for Molecular Medicine and Therapeutics, Vancouver, BC, Canada.
Grunau RE; Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.; BC Children's Hospital Research Institute, Vancouver, BC, Canada.
Źródło:
Pain [Pain] 2017 Aug; Vol. 158 (8), pp. 1586-1598.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: 2015- : Hagerstown, MD : Lippincott Williams & Wilkins
Original Publication: Amsterdam, Elsevier/North-Holland.
MeSH Terms:
Brain/*drug effects
Pain/*drug therapy
Animals ; Animals, Newborn ; Mice, Inbred C57BL ; Pain Management/methods ; Pain Measurement/methods ; Sucrose/pharmacology
References:
Pediatr Res. 2011 Apr;69(4):285-92. (PMID: 21178816)
J Pediatr. 2015 Aug;167(2):292-8.e1. (PMID: 25987534)
Ann Neurol. 2012 Jan;71(1):93-109. (PMID: 22275256)
Am J Perinatol. 2007 Oct;24(9):511-7. (PMID: 17907073)
Neurosci Lett. 1990 Jul 31;115(2-3):137-43. (PMID: 2172870)
Pain. 2008 Nov 15;140(1):167-176. (PMID: 18801618)
Neuroimage. 2013 Sep;78:196-203. (PMID: 23587687)
Neuroimage. 2017 Apr 1;149:233-243. (PMID: 28159689)
Brain Res Bull. 1993;30(5-6):523-7. (PMID: 8384517)
Pain. 2011 Jun;152(6):1391-1397. (PMID: 21402444)
Neuroimage. 2008 Jan 1;39(1):32-9. (PMID: 17942324)
Physiol Behav. 1999 Jun;66(4):627-37. (PMID: 10386907)
JAMA. 2008 Jul 2;300(1):60-70. (PMID: 18594041)
Neuroscience. 2005;134(3):737-44. (PMID: 15987666)
Monogr Soc Res Child Dev. 1994;59(1):I-V, 1-81. (PMID: 8047076)
Neurol Res Int. 2012;2012:858929. (PMID: 22530126)
Neuroscience. 2005;133(1):231-43. (PMID: 15893646)
Neuroimage. 2002 Apr;15(4):870-8. (PMID: 11906227)
Physiol Genomics. 2006 Jan 12;24(2):154-62. (PMID: 16410543)
J Pediatr. 2016 May;172:81-87.e2. (PMID: 26763312)
Neuroimage. 2007 May 1;35(4):1424-33. (PMID: 17408971)
Neonatology. 2014;105(3):218-26. (PMID: 24503902)
Magn Reson Med. 2005 Nov;54(5):1311-6. (PMID: 16215960)
Neurotoxicology. 1989 Fall;10(3):475-83. (PMID: 2696899)
J Neurosci. 1998 Aug 15;18(16):6241-53. (PMID: 9698317)
Arch Pediatr Adolesc Med. 2003 Nov;157(11):1071-4. (PMID: 14609895)
JAMA. 2003 Nov 12;290(18):2419-27. (PMID: 14612478)
Pharmacol Biochem Behav. 2012 Apr;101(2):265-70. (PMID: 22197708)
Pediatrics. 2010 May;125(5):1042-7. (PMID: 20403938)
Lancet. 2004 May 22;363(9422):1673-82. (PMID: 15158628)
Neuroimage. 2008 Aug 1;42(1):60-9. (PMID: 18502665)
Proc Natl Acad Sci U S A. 1997 Feb 18;94(4):1471-5. (PMID: 9037077)
Brain Res Mol Brain Res. 2004 May 19;124(2):134-42. (PMID: 15135221)
Pharmacol Biochem Behav. 1987 Mar;26(3):483-9. (PMID: 3575365)
Prog Neuropsychopharmacol Biol Psychiatry. 2005 Dec;29(8):1249-63. (PMID: 16253410)
Pain. 2013 Oct;154(10):1946-1952. (PMID: 23711638)
Autism Res. 2014 Feb;7(1):124-37. (PMID: 24151012)
Nat Neurosci. 2014 Mar;17(3):341-6. (PMID: 24569830)
Physiol Behav. 2001 May;73(1-2):51-8. (PMID: 11399294)
Pediatr Res. 2009 Sep;66(3):272-7. (PMID: 19531973)
J Neurosci. 2017 Feb 1;37(5):1090-1101. (PMID: 27986927)
Cochrane Database Syst Rev. 2008 Jan 23;(1):CD004212. (PMID: 18254040)
Physiol Behav. 2015 Jun 1;145:84-90. (PMID: 25846434)
Cochrane Database Syst Rev. 2016 Jul 16;7:CD001069. (PMID: 27420164)
PLoS One. 2013 Oct 18;8(10):e76702. (PMID: 24204657)
Pediatrics. 2014 Mar;133(3):412-21. (PMID: 24534406)
Dev Neurobiol. 2013 Jan;73(1):85-97. (PMID: 22821778)
Neurotoxicol Teratol. 2012 Jan-Feb;34(1):47-55. (PMID: 22094261)
Behav Neurosci. 1986 Oct;100(5):624-30. (PMID: 3640642)
Neuropharmacology. 2002 May;42(6):829-36. (PMID: 12015209)
Pediatrics. 2016 Feb;137(2):e20154271. (PMID: 26810788)
Ann Neurol. 2012 Mar;71(3):385-96. (PMID: 22374882)
Pediatr Res. 2007 Sep;62(3):283-90. (PMID: 17551412)
Glia. 2008 Jul;56(9):1017-27. (PMID: 18381654)
Int J Neurosci. 2004 Aug;114(8):1001-11. (PMID: 15527204)
Pediatrics. 2005 Apr;115(4):1004-7. (PMID: 15805377)
Front Behav Neurosci. 2014 Dec 02;8:409. (PMID: 25520635)
Am J Physiol Regul Integr Comp Physiol. 2004 Jan;286(1):R31-7. (PMID: 12933362)
Pediatr Neurol. 2013 Feb;48(2):123-129.e1. (PMID: 23337005)
J Perinatol. 2008 Feb;28(2):107-11. (PMID: 17855806)
Neonatology. 2013;103(1):35-43. (PMID: 23037996)
J Neurosci. 2012 Oct 17;32(42):14775-93. (PMID: 23077062)
J Addict Med. 2009 Mar;3(1):33-41. (PMID: 21768998)
Psychopharmacology (Berl). 2005 May;179(2):349-55. (PMID: 15821952)
Int J Nurs Stud. 2016 Oct;62:118-25. (PMID: 27474944)
Pain. 2013 Mar;154(3):449-458. (PMID: 23352760)
J Pediatr. 2013 Jul;163(1):29-35.e1. (PMID: 23415615)
Pediatrics. 2002 Sep;110(3):523-8. (PMID: 12205254)
Arch Pediatr Adolesc Med. 2001 Feb;155(2):173-80. (PMID: 11177093)
Grant Information:
R01 HD039783 United States HD NICHD NIH HHS; International Canadian Institute of Health Research
Substance Nomenclature:
57-50-1 (Sucrose)
Entry Date(s):
Date Created: 20170718 Date Completed: 20180501 Latest Revision: 20221005
Update Code:
20240104
PubMed Central ID:
PMC5539923
DOI:
10.1097/j.pain.0000000000000961
PMID:
28715355
Czasopismo naukowe
Oral sucrose is administered routinely to reduce pain of minor procedures in premature infants and is recommended as standard care in international guidelines. No human or animal studies on effects of early repeated sucrose exposure on long-term brain development have been done in the context of pain. We evaluated the effects of repeated neonatal sucrose treatment before an intervention on long-term brain structure in mouse pups. Neonatal C57Bl/6J mice (n = 109) were randomly assigned to one of 2 treatments (vehicle vs sucrose) and one of 3 interventions (handling, touch, or needle-prick). Mice received 10 interventions daily from postnatal day 1 to 6 (P1-6). A dose of vehicle or 24% sucrose was given orally 2 minutes before each intervention. At P85-95, brains were scanned using a multichannel 7.0 T MRI. Volumes of 159 independent brain regions were obtained. Early repetitive sucrose exposure in mice (after correcting for whole brain volume and multiple comparisons) lead to smaller white matter volumes in the corpus callosum, stria terminalis, and fimbria (P < 0.0001). Cortical and subcortical gray matter was also affected by sucrose with smaller volumes of hippocampus and cerebellum (P < 0.0001). These significant changes in adult brain were found irrespective of the type of intervention in the neonatal period. This study provides the first evidence of long-term adverse effects of repetitive sucrose exposure and raises concerns for the use of this standard pain management practice during a period of rapid brain development in very preterm infants.

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies