Improvement in insulin sensitivity and prevention of high fat diet-induced liver pathology using a CXCR2 antagonist.


Journal

Cardiovascular diabetology
ISSN: 1475-2840
Titre abrégé: Cardiovasc Diabetol
Pays: England
ID NLM: 101147637

Informations de publication

Date de publication:
12 07 2022
Historique:
received: 16 02 2022
accepted: 28 05 2022
entrez: 13 7 2022
pubmed: 14 7 2022
medline: 16 7 2022
Statut: epublish

Résumé

Liver pathology (LP) characteristic of non-alcoholic fatty acid disease (NAFLD)/non-alcoholic steatohepatitis (NASH) is a prevalent co-morbidity of type 2 diabetes (T2D). Accumulating evidence indicates that neutrophils driving insulin resistance (IR), including hepatic IR, precipitate T2D-associated NAFLD/NASH. We hypothesized that targeting neutrophil accumulation into insulin-sensitive tissues in mice using a CXCR2 antagonist under T2D-precipitating high fat diet (HFD) could improve insulin sensitivity and prevent the progression towards liver pathology reminiscent of NAFLD/NASH. Mice were age-matched and on standard rodent chow prior to 1:1 randomization into control and HFD formulated with the CXCR2 antagonist AZD5069 or with biologically inactive substitute. They were monitored for metabolic changes including insulin sensitivity using the hyperinsulinemic-euglycemic clamp and hepatic histopathologic evaluation in H&E-stained sections as well as via immunofluorescence microscopy of liver sections for leukocyte markers, collagen 1A1 formation, α-smooth muscle actin (SMA), and galectin-3 expression, for 16 weeks. Statistical tests used to determine significant differences among study groups and outcomes include Student's t-test, one-way ANOVA, repeated measures two-way ANOVA, and Fisher's exact test, depending on the analytical question. Compared to mice on HFD, mice in the AZD5069-formulated HFD exhibited improved insulin sensitivity, a modest reduction in weight gain, and a significant improvement in LP and markers related to NAFLD/NASH. Mice in the AZD5069-formulated HFD also exhibited reduced neutrophil accumulation into the liver at the end of the 16 week study period. These results show, for the first time, the effectiveness of a selective CXCR2 antagonist to improve insulin sensitivity, concomitantly preventing the progression towards LP characteristic of NAFLD/NASH. This represents a novel approach to target IR and developing LP under T2D-susceptible conditions using a single agent. Furthermore, our data extend the growing evidence in support of neutrophils as a leukocyte population that imprints and maintains a chronic inflammatory state in the progression of dysregulated metabolism in liver-specific co-morbid conditions.

Sections du résumé

BACKGROUND
Liver pathology (LP) characteristic of non-alcoholic fatty acid disease (NAFLD)/non-alcoholic steatohepatitis (NASH) is a prevalent co-morbidity of type 2 diabetes (T2D). Accumulating evidence indicates that neutrophils driving insulin resistance (IR), including hepatic IR, precipitate T2D-associated NAFLD/NASH. We hypothesized that targeting neutrophil accumulation into insulin-sensitive tissues in mice using a CXCR2 antagonist under T2D-precipitating high fat diet (HFD) could improve insulin sensitivity and prevent the progression towards liver pathology reminiscent of NAFLD/NASH.
METHODS
Mice were age-matched and on standard rodent chow prior to 1:1 randomization into control and HFD formulated with the CXCR2 antagonist AZD5069 or with biologically inactive substitute. They were monitored for metabolic changes including insulin sensitivity using the hyperinsulinemic-euglycemic clamp and hepatic histopathologic evaluation in H&E-stained sections as well as via immunofluorescence microscopy of liver sections for leukocyte markers, collagen 1A1 formation, α-smooth muscle actin (SMA), and galectin-3 expression, for 16 weeks. Statistical tests used to determine significant differences among study groups and outcomes include Student's t-test, one-way ANOVA, repeated measures two-way ANOVA, and Fisher's exact test, depending on the analytical question.
RESULTS
Compared to mice on HFD, mice in the AZD5069-formulated HFD exhibited improved insulin sensitivity, a modest reduction in weight gain, and a significant improvement in LP and markers related to NAFLD/NASH. Mice in the AZD5069-formulated HFD also exhibited reduced neutrophil accumulation into the liver at the end of the 16 week study period.
CONCLUSIONS
These results show, for the first time, the effectiveness of a selective CXCR2 antagonist to improve insulin sensitivity, concomitantly preventing the progression towards LP characteristic of NAFLD/NASH. This represents a novel approach to target IR and developing LP under T2D-susceptible conditions using a single agent. Furthermore, our data extend the growing evidence in support of neutrophils as a leukocyte population that imprints and maintains a chronic inflammatory state in the progression of dysregulated metabolism in liver-specific co-morbid conditions.

Identifiants

pubmed: 35831885
doi: 10.1186/s12933-022-01564-y
pii: 10.1186/s12933-022-01564-y
pmc: PMC9277870
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

130

Informations de copyright

© 2022. The Author(s).

Références

Diabetes. 2006 Feb;55(2):390-7
pubmed: 16443772
Hepatology. 2010 Sep;52(3):913-24
pubmed: 20648476
Am J Pathol. 2022 Jan;192(1):31-42
pubmed: 34710382
J Biol Chem. 2007 Apr 20;282(16):11658-66
pubmed: 17197447
Eur J Immunol. 2015 Sep;45(9):2446-56
pubmed: 26220361
Eur J Biochem. 1998 Jul 1;255(1):67-73
pubmed: 9692902
Nat Med. 2012 Sep;18(9):1407-12
pubmed: 22863787
J Pathol. 2015 Sep;237(1):85-97
pubmed: 25950520
Lab Anim Res. 2018 Dec;34(4):133-139
pubmed: 30671098
Endocrine. 2017 Jul;57(1):72-82
pubmed: 28508193
Am J Physiol Endocrinol Metab. 2019 Dec 1;317(6):E1205-E1217
pubmed: 31573846
J Endocrinol Invest. 2018 May;41(5):509-521
pubmed: 29189999
JAMA Netw Open. 2019 Oct 2;2(10):e1912565
pubmed: 31584681
Thromb Haemost. 2013 Mar;109(3):399-406
pubmed: 23364297
Front Cell Dev Biol. 2018 Nov 12;6:150
pubmed: 30483502
Int J Mol Sci. 2021 Jun 25;22(13):
pubmed: 34202257
J Endocrinol. 2014 Aug;222(2):267-76
pubmed: 24928936
Nutrients. 2019 Jul 05;11(7):
pubmed: 31284400
Curr Opin Hematol. 2014 Jan;21(1):8-15
pubmed: 24275691
J Inflamm (Lond). 2009 Aug 27;6:25
pubmed: 19709445
Cells. 2019 Mar 08;8(3):
pubmed: 30857223
Drugs R D. 2018 Jun;18(2):149-159
pubmed: 29856004
J Clin Transl Hepatol. 2021 Feb 28;9(1):40-50
pubmed: 33604254
Hepatology. 2019 Jun;69(6):2672-2682
pubmed: 30179269
Biochemistry. 1997 Mar 4;36(9):2716-23
pubmed: 9054580
Diabetes Metab Syndr. 2016 Apr-Jun;10(2 Suppl 1):S77-81
pubmed: 26810159
Biochim Biophys Acta. 2014 Mar;1842(3):446-62
pubmed: 23707515
Diabetes. 2005 Dec;54 Suppl 2:S11-7
pubmed: 16306328
J Biol Chem. 1994 Nov 25;269(47):29355-8
pubmed: 7961909
Clin Appl Thromb Hemost. 2014 Mar;20(2):159-63
pubmed: 22992349
Immunity. 2019 Feb 19;50(2):378-389.e5
pubmed: 30784579
J Innate Immun. 2013;5(4):304-14
pubmed: 23571274
J Clin Endocrinol Metab. 2014 Jun;99(6):1983-92
pubmed: 24712577
Front Physiol. 2018 Feb 20;9:113
pubmed: 29515456
J Clin Invest. 2016 Jan;126(1):12-22
pubmed: 26727229
Cell Metab. 2009 Apr;9(4):339-49
pubmed: 19356715
J Clin Invest. 2004 Jul;114(2):147-52
pubmed: 15254578
J Am Assoc Lab Anim Sci. 2017 Jan 1;56(1):95-97
pubmed: 28905722
World J Gastroenterol. 2019 Sep 7;25(33):4904-4920
pubmed: 31543682
Cytokine. 2005 Jul 7;31(1):9-17
pubmed: 15967374
Biomedicines. 2021 Apr 21;9(5):
pubmed: 33919366
Ann Hepatol. 2020 Jul - Aug;19(4):359-366
pubmed: 32349939
Arterioscler Thromb Vasc Biol. 2012 Aug;32(8):1799-808
pubmed: 22723441
Sci Rep. 2017 Dec 4;7(1):16878
pubmed: 29203879
Nat Rev Gastroenterol Hepatol. 2017 Jan;14(1):32-42
pubmed: 27729660
Nagoya J Med Sci. 2020 Aug;82(3):391-397
pubmed: 33132423
Exp Mol Pathol. 2015 Aug;99(1):155-62
pubmed: 26112094
Mol Immunol. 2006 Mar;43(7):897-914
pubmed: 16084593
Gastroenterology. 2020 May;158(6):1611-1625.e12
pubmed: 32027911
J Hepatol. 2019 Oct;71(4):793-801
pubmed: 31279902
Front Immunol. 2020 Jun 24;11:1169
pubmed: 32670278
J Innate Immun. 2022;14(1):4-30
pubmed: 33849008
Circ Res. 2020 May 22;126(11):1590-1612
pubmed: 32437300
Int J Mol Sci. 2018 Jan 26;19(2):
pubmed: 29373564
Biol Rev Camb Philos Soc. 2016 May;91(2):452-68
pubmed: 25740151
Biochem Biophys Res Commun. 2018 Sep 10;503(3):1618-1624
pubmed: 30060948
Clin Gastroenterol Hepatol. 2021 Dec;19(12):2673-2674.e3
pubmed: 33157318
Lancet Respir Med. 2016 Oct;4(10):797-806
pubmed: 27574788
J Diabetes Complications. 2014 Mar-Apr;28(2):226-33
pubmed: 24342268
Nat Rev Gastroenterol Hepatol. 2019 Mar;16(3):145-159
pubmed: 30482910
J Clin Invest. 2006 Jul;116(7):1793-801
pubmed: 16823477
PLoS One. 2018 Dec 11;13(12):e0208634
pubmed: 30533032
Hepatology. 2019 Nov;70(5):1841-1855
pubmed: 31034092
Ann Nutr Metab. 2015;67(4):218-27
pubmed: 26452040
Eur J Immunol. 1998 Jan;28(1):164-70
pubmed: 9485196
J Hepatol. 2019 Nov;71(5):1012-1021
pubmed: 31301321
Int J Obes (Lond). 2006 Sep;30(9):1347-55
pubmed: 16534530
Mol Cell Endocrinol. 2019 Aug 1;493:110480
pubmed: 31176759
Hepatology. 2018 Apr;67(4):1204-1206
pubmed: 29091293
Am J Physiol Gastrointest Liver Physiol. 2011 Nov;301(5):G825-34
pubmed: 21836057
Cells. 2021 Sep 06;10(9):
pubmed: 34571976
J Hepatol. 2022 Mar;76(3):526-535
pubmed: 34710482
PLoS One. 2015 Mar 10;10(3):e0120092
pubmed: 25756662
Eur Med J Hepatol. 2018;6(1):100-109
pubmed: 29930864
J Biol Chem. 2009 Jul 31;284(31):20692-8
pubmed: 19494115
BMC Gastroenterol. 2020 Jul 6;20(1):210
pubmed: 32631250
J Clin Invest. 2011 Jun;121(6):2111-7
pubmed: 21633179
Scand J Immunol. 2020 Nov;92(5):e12971
pubmed: 32892401
Mol Immunol. 1993 Mar;30(4):359-67
pubmed: 8384312
Am J Physiol. 1985 Mar;248(3 Pt 1):E353-62
pubmed: 3883806
QJM. 2012 May;105(5):425-32
pubmed: 22156706
FEBS J. 2022 Jun;289(11):3024-3057
pubmed: 33860630
Expert Opin Ther Targets. 2016;20(5):615-26
pubmed: 26609894

Auteurs

Brett E Phillips (BE)

Institute of Cellular Therapeutics, Allegheny Health Network, 11th Floor South Tower, 320 East North Avenue, Pittsburgh, PA, S15212, USA.

Louise Lantier (L)

Department of Molecular Physiology and Biophysics, Vanderbilt University., Nashville, TN, 37232, USA.

Carl Engman (C)

Institute of Cellular Therapeutics, Allegheny Health Network, 11th Floor South Tower, 320 East North Avenue, Pittsburgh, PA, S15212, USA.

Yesica Garciafigueroa (Y)

Institute of Cellular Therapeutics, Allegheny Health Network, 11th Floor South Tower, 320 East North Avenue, Pittsburgh, PA, S15212, USA.

Aatur Singhi (A)

Department of Pathology, School of Medicine, Room A616.2, UPMC Presbyterian, University of Pittsburgh, 200 Lothrop Street, Pittsburgh, PA, 15213, USA.

Massimo Trucco (M)

Institute of Cellular Therapeutics, Allegheny Health Network, 11th Floor South Tower, 320 East North Avenue, Pittsburgh, PA, S15212, USA.

Christos Mantzoros (C)

Section of Endocrinology, VA Boston Healthcare System, Harvard Medical School, Boston, USA.
Department of Medicine Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

David Wasserman (D)

Department of Molecular Physiology and Biophysics, Vanderbilt University., Nashville, TN, 37232, USA.

Nick Giannoukakis (N)

Institute of Cellular Therapeutics, Allegheny Health Network, 11th Floor South Tower, 320 East North Avenue, Pittsburgh, PA, S15212, USA. nick.giannoukakis@ahn.org.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH