| Name | sodium channel (protein family or complex) |
|---|---|
| Synonyms | Sodium channel |
| Name | rotenone |
|---|---|
| CAS |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 17173871 | Molchanova SM, Oja SS, Saransaari P: Inhibitory effect of on veratridine-evoked D-[3H] release from murine corticostriatal slices: involvement of channels and mitochondria. Brain Res. 2007 Jan 26;1130(1):95-102. Epub 2006 Dec 14. The respiratory chain blocker rotenone or mitochondrial protonophore carbonyl 3-chlorophenylhydrazone (CCCP) in combination with the mitochondrial ATPase inhibitor oligomycin, which inhibits the mitochondrial Ca2+ uniporter, also reduced the effect of We have previously shown that the inhibitory neuromodulator attenuates the release of preloaded D-[3H] from murine corticostriatal slices evoked by ischemic conditions or by application of the sodium channel agonist veratridine. |
1(0,0,0,1) | Details |
| 14505934 | Deng Y, Nicholson RA: Stimulation by surangin B of endogenous amino acid release from synaptosomes. Toxicon. 2003 Sep 15;42(4):351-7. In all cases, these responses were reduced by removing from the saline and surangin B-evoked release of GLU, aspartic acid (ASP) and was significantly inhibited by the sodium channel blocker tetrodotoxin. Rotenone (a complex I inhibitor) and carbonyl chlorophenylhydrazone (CCCP; an uncoupler), were more potent releasers of amino acids from synaptosomes than surangin B, however, carboxin (a complex II-selective inhibitor), was extremely weak to ineffective in this regard. |
1(0,0,0,1) | Details |