SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:umu-5986"
 

Search: onr:"swepub:oai:DiVA.org:umu-5986" > Inhibition of fatty...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Inhibition of fatty acid amide hydrolase, a key endocannabinoid metabolizing enzyme, by analogues of ibuprofen and indomethacin.

Holt, Sandra (author)
Paylor, Ben (author)
Boldrup, Linda (author)
show more...
Alajakku, Kirsi (author)
Vandevoorde, Séverine (author)
Sundström, Anna (author)
Cocco, Maria Teresa (author)
Onnis, Valentina (author)
Fowler, Christopher J (author)
Umeå universitet,Farmakologi
show less...
 (creator_code:org_t)
Elsevier B.V. 2007
2007
English.
In: European Journal of Pharmacology. - : Elsevier B.V.. - 0014-2999 .- 1879-0712. ; 565:1-3, s. 26-36
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • There is evidence in the literature that the nonsteroidal anti-inflammatory drugs indomethacin and ibuprofen can interact with the cannabinoid system both in vitro and in vivo. In the present study, a series of analogues of ibuprofen and indomethacin have been investigated with respect to their ability to inhibit fatty acid amide hydrolase, the enzyme responsible for the hydrolysis of the endogenous cannabinoid anandamide. Of the fourteen compounds tested, the 6-methyl-pyridin-2-yl analogue of ibuprofen (“ibu-am5”) was selected for further study. This compound inhibited rat brain anandamide hydrolysis in a non-competitive manner, with IC50 values of 4.7 and 2.5 μM being found at pH 6 and 8, respectively. By comparison, the IC50 values for ibuprofen were 130 and 750 μM at pH 6 and 8, respectively. There was no measurable N-acylethanolamine hydrolyzing acid amidase activity in rat brain membrane preparations. In intact C6 glioma cells, ibu-am5 inhibited the hydrolysis of anandamide with an IC50 value of 1.2 μM. There was little difference in the potencies of ibu-am5 and ibuprofen towards cyclooxygenase-1 and -2 enzymes, and neither compound inhibited the activity of monoacylglycerol lipase. Ibu-am5 inhibited the binding of [3H]-CP55,940 to rat brain CB1 and human CB2 cannabinoid receptors more potently than ibuprofen, but the increase in potency was less than the corresponding increase in potency seen for inhibition of FAAH activity. It is concluded that ibu-am5 is an analogue of ibuprofen with a greater potency towards fatty acid amide hydrolase but with a similar cyclooxygenase inhibitory profile, and may be useful for the study of the therapeutic potential of combined fatty acid amide hydrolase–cyclooxygenase inhibitors.

Keyword

Anandamide
Fatty acid amide hydrolase
Cyclooxygenase
Nonsteroidal anti-inflammatory drug
Cannabinoid receptor

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view