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Substance P

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|- | align="center" colspan="2" |
|- | colspan="2" bgcolor="#dddddd" | Identifiers |- | bgcolor="#e7dcc3" | Symbol(s) | bgcolor="#eeeeee" | [TAC1] TAC2, NKNA |- | bgcolor="#e7dcc3" | Entrez | bgcolor="#eeeeee" | [6863] |- class="hiddenStructure" | bgcolor="#e7dcc3" | OMIM | bgcolor="#eeeeee" | [162320] |- | bgcolor="#e7dcc3" | RefSeq | bgcolor="#eeeeee" | [NM_003182] |- | bgcolor="#e7dcc3" | UniProt | bgcolor="#eeeeee" | [P20366] |- class="hiddenStructure" | bgcolor="#e7dcc3" | PDB | bgcolor="#eeeeee" | [] |- | colspan="2" bgcolor="#dddddd" | Other data |- class="hiddenStructure" | bgcolor="#e7dcc3" | EC number | bgcolor="#eeeeee" | [] |- | bgcolor="#e7dcc3" | Locus | bgcolor="#eeeeee" | Chr. 7[q21-q22] |- |}
|- | align="center" colspan="2" |
|- | colspan="2" bgcolor="#dddddd" | Identifiers |- | bgcolor="#e7dcc3" | Symbol(s) | bgcolor="#eeeeee" | [TACR1] TAC1R |- | bgcolor="#e7dcc3" | Entrez | bgcolor="#eeeeee" | [6869] |- class="hiddenStructure" | bgcolor="#e7dcc3" | OMIM | bgcolor="#eeeeee" | [162323] |- | bgcolor="#e7dcc3" | RefSeq | bgcolor="#eeeeee" | [NM_001058] |- | bgcolor="#e7dcc3" | UniProt | bgcolor="#eeeeee" | [P25103] |- class="hiddenStructure" | bgcolor="#e7dcc3" | PDB | bgcolor="#eeeeee" | [] |- | colspan="2" bgcolor="#dddddd" | Other data |- class="hiddenStructure" | bgcolor="#e7dcc3" | EC number | bgcolor="#eeeeee" | [] |- | bgcolor="#e7dcc3" | Locus | bgcolor="#eeeeee" | Chr. 2[p13.1-p12] |- |} In neuroscience, Substance P is a neuropeptide: a short-chain polypeptide that functions as a neurotransmitter and as a neuromodulator. It belongs to the tachykininneuropeptide family.

Substance P is an 11-amino acid polypeptide with the sequence: Arg Pro Lys Pro Gln Gln Phe Phe Gly Leu Met NH2. In central nervous system substance P has been associated in the regulation of mood disorders, anxiety, stress, reinforcement, neurogenesis, respiratory rhythm, neurotoxicity, nausea / emesis and pain.

It also has effects as a potent vasodilator. This is caused by the release of nitric oxide from the endothelium. Its release can cause hypotension.

The endogenous receptor for Substance P is neurokinin 1 receptor (NK1-receptor, NK1R). It belongs to the tachykinin receptor sub-family of GPCRs.

Substance P antagonist (SPA) aprepitant is available in the market in the treatment of chemotherapy-induced nausea / emesis.

Substance P is involved in the transmission of pain impulses from peripheral receptors to the central nervous system. It has been theorised that it plays a part in fibromyalgia. Capsaicin has been shown to reduce the levels of Substance P probably by reducing the number of C-fibre nerves or causing these nerves to be more tolerant.

Naked Mole Rats lack Substance P and do not feel pain when painful stimuli are administered.

External links

  • http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=36511 Substance P in PubChem

 


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