Protein Information

ID 447
Name P10
Synonyms CGI 102; p10; EXOSC 3; EXOSC3; Exosome complex exonuclease RRP40; Exosome component 3; Exosome component Rrp40; RP11 3J10.8…

Compound Information

ID 336
Name strychnine
CAS strychnidin-10-one

Reference

PubMed Abstract RScore(About this table)
19720114 Cooke JE, Mathers DA, Puil E: Isovaline causes inhibition by increasing potassium conductance in thalamic neurons. Neuroscience. 2009 Dec 15;164(3):1235-43. Epub 2009 Aug 28.
The rare amino acid isovaline has analgesic properties in pain models and is a structural analogue of the inhibitory neurotransmitter glycine. Glycinergic inhibition is prevalent in pain pathways. In this paper, we examined the possibility that isovaline inhibits neurons by activating strychnine (Str)-sensitive glycine (A) receptors in ventrobasal thalamus. Sagittal brain sections containing ventrobasal nuclei were prepared from P10-P15 rats. Whole-cell recordings were made in current-clamp and voltage-clamp modes. R-isovaline (R-Iva) increased input conductance and hyperpolarized the membrane. The conductance increase shunted action potentials and low-threshold Ca (2+) spikes evoked by current pulse injection. Unlike the Cl (-)-mediated responses to glycine, isovaline responses were insensitive to Str antagonism and usually not reversible. The concentration-response curve was non-sigmoidal, rising to a maximum at approximately 100 microM, and thereafter declining in amplitude. Current-voltage relationships showed that isovaline increased inward and outward rectification. The isovaline current reversed polarity close to the K (+) equilibrium potential. The relationships were negligibly affected by tetrodotoxin (TTX), chelation of intracellular Ca (2+) or blockade of the hyperpolarization-activated current, I (h). Internal Cs (+) and external Ba (2+) or Cs (+) prevented isovaline responses. In conclusion, isovaline inhibited firing mainly by activating rectifying and possibly leak K (+) currents. Isovaline-induced changes shunted action potentials and suppressed rebound excitation in ventrobasal neurons, as expected for analgesic actions.
1(0,0,0,1)