Macquarie Home | Course Handbook | Library | Campus Map | Macquarie Contacts
Home page

Macquarie University ResearchOnline

Home
Add
-List Of Titles -Orexin A in rat rostral ventrolateral medulla is pressor, sympathoexcitatory, increases barosensitivity and attenuates the somatosympathetic reflex

Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.14/163083

OpenURL Link
23 Visitors 24 Hits 0 Downloads
Title
Orexin A in rat rostral ventrolateral medulla is pressor, sympathoexcitatory, increases barosensitivity and attenuates the somatosympathetic reflex
Related
British journal of pharmacology, Vol. 165, Issue 7, (2012), p.2292-2303
DOI
10.1111/j.1476-5381.2011.01694.x
Publisher
British Pharmacological Society
Date
2012
Author/Creator
Shahid, Israt Z
Author/Creator
Rahman, Ahmed A
Author/Creator
Pilowsky, Paul M
Description
Background: The rostral ventrolateral medulla (RVLM) maintains sympathetic nerve activity (SNA), and integrates adaptive reflexes. Orexin A (OX-A)-immunoreactive (-ir) neurones in the lateral hypothalamus project to the RVLM. Microinjection of OX-A into RVLM increases blood pressure and heart rate (HR). The expression of orexin receptors, and effect of OX-A in the RVLM on splanchnic SNA (sSNA), respiration and adaptive reflexes is unknown. Experimental approach: The effect of OX-A on baseline cardiorespiratory variables as well as the somatosympathetic, baroreceptor and chemoreceptor reflexes in RVLM were investigated in urethane-anaesthetized, vagotomized and artificially ventilated male Sprague-Dawley rats (n = 49). OX-A and its receptors were detected with fluorescence immunohistochemistry. Key results: RVLM tyrosine hydroxylase-ir (TH-ir) neurones were frequently colocalised with orexin receptor 1 (OX₁) and orexin receptor 2 (OX₂), and closely apposed by OX-A-ir terminals. RVLM injection of OX-A is pressor and sympathoexcitatory. The peak effect was observed at 50 pmol with increase in mean arterial pressure (MAP) and SNA of 42 mmHg and 45 % from baseline, respectively. The responses to OX-A (50 pmol) were attenuated by the OX₁ antagonist, SB334867, and reproduced by the OX₂ agonist, [Ala₁₁, D-Leu₁₅]orexin B. OX-A attenuated the somatosympathetic reflex but increased baroreflex sensitivity. OX-A increased or reduced the sympathoexcitation following hypoxia or hypercapnia respectively. Conclusions: The results demonstrate that while the central cardiorespiratory control mechanisms at rest do not rely on orexin, responses to adaptive stimuli are dramatically affected by the functional state of orexin receptors.
Description
12 page(s)
Subject Keyword
Orexin A
Subject Keyword
sympathetic vasomotor tone
Subject Keyword
somatosympathetic reflex
Subject Keyword
baroreflex
Subject Keyword
chemoreflex
Resource Type
journal article
Organisation
Macquarie University. Australian School of Advanced Medicine

Identifier
http://hdl.handle.net/1959.14/163083
Identifier
ISSN:0007-1188
Identifier
mq-rm-2011005289
Identifier
mq_res-20111202-090534
Language
eng
Reviewed
Reviewed
Save/E-mail Citation
Citation Format
E-mail Address
Subject
"British journal of pharmacology"
 
OR
  • Show All  
  • Show My Selections 
Advanced Search

Search

Rahman, Ahmed A
chemoreflex
baroreflex

Browse

  • By Title 
  • By Author/Creator 
  • By Department/Centre 
  • By Subject Keyword 
  • By Journal/Conference 
  • By FoR/RFCD codes 
  • By Resource Type 
  • By Date 

Highlights

  • Most Accessed Objects 
  • Recent Additions 
  • Pending Publications 
  • Author Profiles 

Resources

  • About ResearchOnline 
  • FAQ 
  • Open Access 
  • Open Access-FAQs 
  • Copyright 
  • Contribute 
  • Help 
  • Contact
  • Terms and Conditions 
Valid XHTML 1.0 Strict Powered by VITAL

Copyright Macquarie University | Privacy Statement | Accessibility Information

ABN 90 952 801 237 | CRICOS Provider No 00002J

Library Staff Sign In