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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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Publisher copy:
10.1042/cs20180150

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Role:
Author
ORCID:
0000-0003-3231-7267


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:
1470-8736
ISSN:
0143-5221
Pmid:
30467191


Language:
English
Keywords:
Pubs id:
pubs:946272
UUID:
uuid:eee5b083-be7e-4ba0-9ee0-b00d5b3c9783
Local pid:
pubs:946272
Source identifiers:
946272
Deposit date:
2019-01-31

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