TRPV1: A Potential Therapeutic Target in Type 2 Diabetes and Comorbidities?

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

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TRPV1 : A Potential Therapeutic Target in Type 2 Diabetes and Comorbidities? / Gram, Dorte X; Holst, Jens J; Szallasi, Arpad.

I: Trends in Molecular Medicine, Bind 23, Nr. 11, 11.2017, s. 1002-1013.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Gram, DX, Holst, JJ & Szallasi, A 2017, 'TRPV1: A Potential Therapeutic Target in Type 2 Diabetes and Comorbidities?', Trends in Molecular Medicine, bind 23, nr. 11, s. 1002-1013. https://doi.org/10.1016/j.molmed.2017.09.005

APA

Gram, D. X., Holst, J. J., & Szallasi, A. (2017). TRPV1: A Potential Therapeutic Target in Type 2 Diabetes and Comorbidities? Trends in Molecular Medicine, 23(11), 1002-1013. https://doi.org/10.1016/j.molmed.2017.09.005

Vancouver

Gram DX, Holst JJ, Szallasi A. TRPV1: A Potential Therapeutic Target in Type 2 Diabetes and Comorbidities? Trends in Molecular Medicine. 2017 nov.;23(11):1002-1013. https://doi.org/10.1016/j.molmed.2017.09.005

Author

Gram, Dorte X ; Holst, Jens J ; Szallasi, Arpad. / TRPV1 : A Potential Therapeutic Target in Type 2 Diabetes and Comorbidities?. I: Trends in Molecular Medicine. 2017 ; Bind 23, Nr. 11. s. 1002-1013.

Bibtex

@article{add19ad3ec544a8983832e7467f28820,
title = "TRPV1: A Potential Therapeutic Target in Type 2 Diabetes and Comorbidities?",
abstract = "With an estimated 422 million affected patients worldwide in 2016, type 2 diabetes (T2D) has reached pandemic proportions and represents a major unmet medical need. T2D is a polygenic disease with a chronic, low-grade inflammatory component. Second-generation transient receptor potential vanilloid-1 (TRPV1) antagonists are potent anti-inflammatory agents with proven clinical safety. In rodent models of T2D, TRPV1 blockade was shown to halt disease progression and improve glucose metabolism. Thus, we propose that TRPV1 antagonists merit further study as novel therapeutic approaches to potentially treat T2D and its comorbidities.",
keywords = "Journal Article, Review",
author = "Gram, {Dorte X} and Holst, {Jens J} and Arpad Szallasi",
note = "Copyright {\textcopyright} 2017 Elsevier Ltd. All rights reserved.",
year = "2017",
month = nov,
doi = "10.1016/j.molmed.2017.09.005",
language = "English",
volume = "23",
pages = "1002--1013",
journal = "Trends in Molecular Medicine",
issn = "1471-4914",
publisher = "Elsevier Ltd. * Trends Journals",
number = "11",

}

RIS

TY - JOUR

T1 - TRPV1

T2 - A Potential Therapeutic Target in Type 2 Diabetes and Comorbidities?

AU - Gram, Dorte X

AU - Holst, Jens J

AU - Szallasi, Arpad

N1 - Copyright © 2017 Elsevier Ltd. All rights reserved.

PY - 2017/11

Y1 - 2017/11

N2 - With an estimated 422 million affected patients worldwide in 2016, type 2 diabetes (T2D) has reached pandemic proportions and represents a major unmet medical need. T2D is a polygenic disease with a chronic, low-grade inflammatory component. Second-generation transient receptor potential vanilloid-1 (TRPV1) antagonists are potent anti-inflammatory agents with proven clinical safety. In rodent models of T2D, TRPV1 blockade was shown to halt disease progression and improve glucose metabolism. Thus, we propose that TRPV1 antagonists merit further study as novel therapeutic approaches to potentially treat T2D and its comorbidities.

AB - With an estimated 422 million affected patients worldwide in 2016, type 2 diabetes (T2D) has reached pandemic proportions and represents a major unmet medical need. T2D is a polygenic disease with a chronic, low-grade inflammatory component. Second-generation transient receptor potential vanilloid-1 (TRPV1) antagonists are potent anti-inflammatory agents with proven clinical safety. In rodent models of T2D, TRPV1 blockade was shown to halt disease progression and improve glucose metabolism. Thus, we propose that TRPV1 antagonists merit further study as novel therapeutic approaches to potentially treat T2D and its comorbidities.

KW - Journal Article

KW - Review

U2 - 10.1016/j.molmed.2017.09.005

DO - 10.1016/j.molmed.2017.09.005

M3 - Review

C2 - 29137713

VL - 23

SP - 1002

EP - 1013

JO - Trends in Molecular Medicine

JF - Trends in Molecular Medicine

SN - 1471-4914

IS - 11

ER -

ID: 189623760