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Nitric oxide synthase expressions in mice skeletal muscle subjected to ischemia/reperfusion injury.

Abstract
Nitric oxide synthase (NOS) expressions in skeletal muscle subjected to ischemia/reperfusion (I/R) were studied using a hind limb tourniquet ischemia model in mice. A rubber band was applied to a hind limb for 3 h under isoflurane anesthesia followed by 1 or 4 h of reperfusion. Increased NADPH diaphorase activity and NOS immunoreactivity were histochemically detected in the cells of muscle that had been subjected to I/R. The results of RT-PCR of the muscle subjected to I/R showed that NOS mRNA expressions were not significantly increased until 4 h after the start of reperfusion. Since there was no significant difference between histochemical findings or between water contents of the hind limbs or organs in interleukin (IL)-6-deficient mice and the wild-type mice, IL-6 may not be involved in the early stage of I/R muscle injury such as that in this model. O(2)(-) production in the cells of muscle that had been subjected to I/R was observed using an in situ detection method with hydroethidine, and the O(2)(-) was inhibited by intravenous administration of L-NAME or L-NMMA, but not L-NIL, 30 min before tourniquet release. Further study is needed to evaluate the role of O(2)(-) produced by constitutive NOS in muscle subjected to I/R in the pathophysiology of tourniquet shock.
AuthorsHirobumi Gunji, Emiko Kurisaki, Miwako Suto, Sumiko Abe, Kouichi Hiraiwa
JournalLegal medicine (Tokyo, Japan) (Leg Med (Tokyo)) Vol. 5 Suppl 1 Pg. S217-20 (Mar 2003) ISSN: 1344-6223 [Print] Ireland
PMID12935594 (Publication Type: Journal Article)
Chemical References
  • Interleukin-6
  • RNA, Messenger
  • Nitric Oxide Synthase
  • NADPH Dehydrogenase
Topics
  • Animals
  • Interleukin-6 (deficiency)
  • Male
  • Mice
  • Models, Animal
  • Muscle, Skeletal (metabolism)
  • NADPH Dehydrogenase (metabolism)
  • Nitric Oxide Synthase (metabolism)
  • RNA, Messenger (metabolism)
  • Reperfusion Injury (metabolism)
  • Reverse Transcriptase Polymerase Chain Reaction

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