substance-p--arg(1)-pro(2)-trp(7)-(9)-leunh(2)(11)- and Inflammation

substance-p--arg(1)-pro(2)-trp(7)-(9)-leunh(2)(11)- has been researched along with Inflammation* in 2 studies

Other Studies

2 other study(ies) available for substance-p--arg(1)-pro(2)-trp(7)-(9)-leunh(2)(11)- and Inflammation

ArticleYear
Effect of neurokinin A, substance P and calcitonin gene related peptide in peripheral hyperalgesia in the rat paw.
    Neuroscience letters, 1991, Mar-11, Volume: 124, Issue:1

    The effect of neurokinin A (NKA), substance P (SP) and calcitonin gene-related peptide (CGRP) in peripheral hyperalgesia was studied in rats using a modification of the Randall-Selitto paw test. NKA was 10 times more potent than SP which was 500 times more potent than CGRP in inducing hyperalgesia in the rat paw, suggesting that NKA and SP but not CGRP could have an important role in acute hyperalgesic conditions. Furthermore, sensitization induced by several injections of subthreshold doses of NKA or CGRP suggest that these neuropeptides along with SP could participate as mediators or modulators of chronic pain.

    Topics: Animals; Calcitonin Gene-Related Peptide; Hyperalgesia; Inflammation; Male; Neurokinin A; Nociceptors; Rats; Rats, Inbred Strains; Substance P

1991
Substance P and peripheral inflammatory hyperalgesia.
    Pain, 1989, Volume: 38, Issue:1

    The hyperalgesic effect of substance P (SP) is usually described as presenting short latency. We now report that multiple injections of sub-threshold doses of SP into the foot pad of a hind paw of rats pre-treated with indomethacin induced a long-lasting hyperalgesia, sensitizing the paw to further challenges with small doses of SP, dopamine or prostacyclin. The sensitizing process also occurred after multiple injections of prostacyclin or prostaglandin E2. The sensitizing effect induced by SP, prostaglandin E2 or prostacyclin is inhibited by pre-treatment with the SP antagonist (D-Arg, D-Pro, D-Trp, Leu)-SP. We suggest that SP has an important role as a modulator in peripheral inflammatory pain by sensitizing nociceptors to its own action and to the action of different mediators. This sensitizing process could also be associated with chronic inflammatory pain.

    Topics: Animals; Dose-Response Relationship, Drug; Hyperalgesia; Hyperesthesia; Inflammation; Male; Pain; Rats; Rats, Inbred Strains; Substance P

1989