Journal article
Functional cardiac orexin receptors: role of orexin-B/orexin 2 receptor in myocardial protection
- Abstract:
- Orexins/hypocretins exert cardiovascular effects which are centrally mediated. In the present study, we tested whether orexins and their receptors may also act in an autocrine/paracrine manner in the heart exerting direct effects. Quantitative reverse transcription-PCR (RT-PCR), immunohistochemical and Western blot analyses revealed that the rat heart expresses orexins and orexin receptors (OXR). In isolated rat cardiomyocytes, only orexin-B (OR-B) caused an increase in contractile shortening, independent of diastolic or systolic calcium levels. A specific orexin receptor-2 (OX2R) agonist ([Ala11, d-Leu15]-Orexin B) exerted similar effects as OR-B, whereas a specific orexin receptor-1 (OX1R) antagonist (SB-408124) did not alter the responsiveness of OR-B. Treatment of the same model with OR-B resulted in a dose-dependent increase in myosin light chain and troponin-I (TnI) phosphorylation. Following ischaemia/reperfusion in the isolated Langendorff perfused rat heart model, OR-B, but not OR-A, exerts a cardioprotective effect; mirrored in an in vivo model as well. Unlike OR-A, OR-B was also able to induce extracellular signal-regulated kinase (ERK) 1/2 (ERK1/2) and Akt phosphorylation in rat myocardial tissue and ERK1/2 phosphorylation in human heart samples. These findings were further corroborated in an in vivo rat model. In human subjects with heart failure, there is a significant negative correlation between the expression of OX2R and the severity of the disease clinical symptoms, as assessed by the New York Heart Association (NYHA) functional classification. Collectively, we provide evidence of a distinct orexin system in the heart that exerts a cardioprotective role via an OR-B/OX2R pathway.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 2.1MB, Terms of use)
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- Publisher copy:
- 10.1042/cs20180150
Authors
- Publisher:
- Portland Press
- Journal:
- Clinical Science More from this journal
- Volume:
- 132
- Issue:
- 24
- Pages:
- 2547-2564
- Publication date:
- 2018-12-13
- Acceptance date:
- 2018-11-22
- DOI:
- EISSN:
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1470-8736
- ISSN:
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0143-5221
- Pmid:
-
30467191
- Language:
-
English
- Keywords:
- Pubs id:
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pubs:946272
- UUID:
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uuid:eee5b083-be7e-4ba0-9ee0-b00d5b3c9783
- Local pid:
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pubs:946272
- Source identifiers:
-
946272
- Deposit date:
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2019-01-31
Terms of use
- Copyright holder:
- Patel et al
- Copyright date:
- 2018
- Notes:
-
Copyright © 2018 The Authors.
This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND).
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