SCIRP Mobile Website

Why Us? >>

  • - Open Access
  • - Peer-reviewed
  • - Rapid publication
  • - Lifetime hosting
  • - Free indexing service
  • - Free promotion service
  • - More citations
  • - Search engine friendly

Free SCIRP Newsletters>>

Add your e-mail address to receive free newsletters from SCIRP.


Contact Us >>

WhatsApp  +86 18163351462(WhatsApp)
Paper Publishing WeChat
Book Publishing WeChat

Article citations


Ewart, M.A., Kennedy, S., Macmillan, D., Raja, A.L., Watt, I.M. and Currie, S. (2014) Altered Vascular Smooth Muscle Function in the ApoE Knockout Mouse during the Progression of Atherosclerosis. Atherosclerosis, 234, 154-161.

has been cited by the following article:

  • TITLE: Effect of Peroxynitrite (ONOO-) on the Function of Murine Perivascular Adipose Tissue

    AUTHORS: Azizah Binti Ugusman, Alex Riddell, Simon Kennedy

    KEYWORDS: Perivascular Adipose Tissue (PVAT), Peroxynitrite, Nitric Oxide, Adiponectin, Anticontractile

    JOURNAL NAME: Pharmacology & Pharmacy, Vol.10 No.4, April 23, 2019

    ABSTRACT: Perivascular adipose tissue (PVAT) surrounds the exterior of blood vessels and releases numerous substances such as adiponectin which positively modulate blood vessel tone. In some cardiovascular diseases such as diabetes and high blood pressure, the function of PVAT changes and we speculate that oxidant stress may play a role in this change. PVAT has the ability to generate both superoxide and nitric oxide and these can combine rapidly under physiological conditions to form peroxynitrite (ONOO-). In disease states, the production of ONOO- may be increased and so its effect on the function of PVAT is of great interest. Consequently, we studied the effects of acute addition of the oxidant species ONOO- on vascular tone and production of adiponectin by mouse thoracic aortic PVAT. Murine PVAT was immunostained for nitrotyrosine, indicating that ONOO- is formed in the PVAT. Exogenous ONOO- significantly increased the anticontractile effect of PVAT via increased adiponectin content but had no effect on eNOS expression or phosphorylation. These results suggest that generation of ONOO- within PVAT may be an important regulatory mechanism which influences the activity of PVAT. The effect of chronic exposure to raised levels of ONOO- on PVAT function remains to be determined.