Nitric oxide mediates long‐term hyperalgesic and antinociceptive effects of the N‐terminus of substance P in the formalin assay in mice
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Summary
The hypothesis that an accumulation of SP N‐terminal metabolites, either peripherally or within the spinal cord area, is sufficient for long‐term modulation of multiple types of nociception with hyperalgesic responses being most persistent is supported.
- Type
- article
- Published
- 1996-10-01
- Cited by
- 28
- References
- 49
- OpenAlex
- https://openalex.org/W2041917376
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:31260765
Keywords
Nociception, Nitric oxide, Substance P, Chemistry, Pharmacology
References
- Extracellular Amino Acid Concentrations in the Dorsal Spinal Cord of Freely Moving Rats Following Veratridine and Nociceptive Stimulation
- The NH2-terminus of substance P modulates NMDA-induced activity in the mouse spinal cord
- Amino terminus of substance P potentiates kainic acid-induced activity in the mouse spinal cord
- The contribution of excitatory amino acids to central sensitization and persistent nociception after formalin-induced tissue injury
- Specific binding of substance P aminoterminal heptapeptide [SP(1-7)] to mouse brain and spinal cord membranes
- Roles of substance P and somatostatin on transmission of nociceptive information induced by formalin in spinal cord.
- Noxious heating of the skin releases immunoreactive substance P in the substantia gelatinosa of the cat: a study with antibody microprobes.
- Effects of substance P on functionally identified units in cat spinal cord.
- Neurokinin and NMDA antagonists (but not a kainic acid antagonist) are antinociceptive in the mouse formalin model
- l‐NG‐nitro arginine methyl ester exhibits antinociceptive activity in the mouse
- Characterization of the hyperalgesic effect induced by intrathecal injection of substance P.
- Elevated CSF levels of substance P and high incidence of Raynaud phenomenon in patients with fibromyalgia: new features for diagnosis
- Antinociceptive actions of different classes of excitatory amino acid receptor antagonists in mice.
- Antinociceptive effects in the formalin and capsaicin tests after intrathecal administration of substance P analogues in mice.
- Substance P and peripheral inflammatory hyperalgesia
- Correlation of substance P-induced desensitization with substance P amino terminal metabolites in the mouse spinal cord.
- Enhanced release of immunoreactive CGRP and substance P from spinal dorsal horn slices occurs during carrageenan inflammation.
- Hyperalgesia produced by intrathecal substance P and related peptides: desensitization and cross desensitization
- Immunoreactive substance P release from skin nerves in the rat by noxious thermal stimulation.
- Central nervous system plasticity in the tonic pain response to subcutaneous formalin injection.
Cited by
- Neuronal nitric oxide synthase (nNOS) mRNA is down‐regulated, and constitutive NOS enzymatic activity decreased, in thoracic dorsal root ganglia and spinal cord of the rat by a substance P N‐terminal metabolite
- NOS inhibitors exhibit antinociceptive properties in the rat formalin test
- Involvement of Nitric Oxide in the Nociceptive Behavioral Reaction in Mice with Tonic Pain
- NOS inhibitor antagonism of PGE2-induced mechanical sensitization of cutaneous C-fiber nociceptors in the rat.
- Dual effect of local application of nitric oxide donors in a model of incision pain in rats.
- Inhibition of ERK phosphorylation by substance P N-terminal fragment decreases capsaicin-induced nociceptive response.
- Evidence that nitric oxide‐ and opioid‐containing interneurons innervate vessels in the dorsal horn of the spinal cord of rats
- An antagonist of substance P N-terminal fragments, D-substance P(1-7), reveals that both nociceptive and antinociceptive effects are induced by substance P N-terminal activity during noxious chemical stimulation.
- Relevance of nitric oxide in pain mechanisms and pain management
- Nitric oxide involvement in the anxiogenic-like effect of substance P.
- The role of PPARs in the microvascular dysfunction in diabetes.
- Modulation of peripheral inflammation by the substance P N-terminal metabolite substance P1-7.
- Effects of substance P fragments on pathological pain
- Nitric oxide from the laterodorsal tegmental neurons: its possible retrograde modulation on norepinephrine release from the axon terminal of the locus coeruleus neurons.
- Inhibition of substance P release from spinal cord tissue after pretreatment with capsaicin does not mediate the antinociceptive effect of capsaicin in adult mice
- Neurokinin 1 receptor distribution in cholinergic neurons and targets of substance P terminals in the rat nucleus accumbens
- Reactive nitroxidative species and nociceptive processing: determining the roles for nitric oxide, superoxide, and peroxynitrite in pain
- Mutual antagonism between nerve growth factor and substance P N-terminal activity on nociceptive activity in mice.
- Synergistic interaction between meloxicam and aminoguanidine in formalin‐induced nociception in mice
- Suppressed Injury-Induced Rise in Spinal Prostaglandin E2 Production and Reduced Early Thermal Hyperalgesia in iNOS-Deficient Mice
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