Table 1.
Toxins and inhibitors of mitochondrial respiratory complexes.
Complexes | Toxins/Inhibitors | Mechanism of Action | References |
---|---|---|---|
Complex-I | Rotenone | Inhibition of electron transport from the iron-sulfur centers in complex I to ubiquinone. | [26] |
Myxothiazol | Inhibits mitochondrial respiration in the bc1 complex of the respiratory chain. | ||
Metformin | Directly targeting ETC complex 1, resulting in inhibition of ATP synthesis | [27] | |
Complex-II | Thenoyltrifluoroacetone (TTFA) | Inhibits complex-II by binding to two ubiquinone binding sites, Qp and Qd. | [28] |
2-[1-Methylhexyl]-4,6-Dinitrophenol | Targets succinate dehydrogenase flavoprotein subunit. | ||
Complex-III | Antimycins | Prevents transfer of electrons from cytochrome b to c1 | [29] |
Ubiquinone Q2, B-2-Octylglucoside |
Targets ubiquinol-cytochrome c reductase iron-sulphur subunit | ||
Complex-IV | Cyanide | Binds with iron and prevent transfer of electrons. | [30] |
Carbon Monoxide | Binds with the reduced form of iron in the heme groups and blocks transfer of electrons to oxygen. | [31] | |
Azide | Reacts with ferric form of Complex-IV and blocks further electron flow. | [32] | |
Complex-V | Efrapeptin | F1-targeting, binding pocket localized in α, β and γ subunits | [33] |
Oligomycin | Binds to the Fo subunit and inhibits the apoptosis induced by Bax | ||
Aurovertin B | Localized mainly in the β subunit. |