Protein Information

ID 3044
Name ubiquinone reductase
Synonyms B13; CI 13KD B; Complex I subunit B13; Complex I 13kD B; NADH Ubiquinone oxidoreductase 1 alpha subcomplex 5; NADH Ubiquinone oxidoreductase subunit B13; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5; NADH ubiquinone oxidoreductase 13 kDa B subunit…

Compound Information

ID 1341
Name rotenone
CAS

Reference

PubMed Abstract RScore(About this table)
11325348 Cormier A, Morin C, Zini R, Tillement JP, Lagrue G: In vitro effects of nicotine on mitochondrial respiration and superoxide anion generation. Brain Res. 2001 May 4;900(1):72-9.
In this study, we investigated the effects of nicotine on rat brain mitochondria. The polarographic studies determined the effects on the respiratory chain, whereas enzymatic assays and [3H]-nicotine binding allowed us to precisely identify its target and site of action. The measurements of oxygen consumption showed a significantly concentration-dependent inhibition by nicotine (EC50 was 4.95x10 (-11) M), and a maximal decrease of 23.90% at 10 (-7) M. Nicotine bound to complex I of the respiratory chain and inhibited the NADH-Ubiquinone reductase activity. We also showed that nicotine and NADH were competitive on complex I. Effects of cotinine, the main nicotine metabolite, and nornicotine, were also investigated: nornicotine inhibited the mitochondrial respiration whereas cotinine did not. Because the complex I generates superoxide anion, we investigated the effects of nicotine, following NBT oxidation, and showed that nicotine was able to inhibit this reactive oxygen species (ROS) generation by 15.74% with an EC50 of 2.02x10 (-11) M. In conclusion, the present study shows that nicotine interacts with the complex I of brain mitochondrial respiratory chain and decreases ROS generation. This may explain a part of the beneficial and protective effects of nicotine in few neurodegenerative diseases, as suggested by many epidemiological studies.
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