Paradoxical lower sensitivity of Locus Coeruleus than Substantia Nigra pars compacta neurons to acute actions of rotenone

• Published in: Experimental neurology 2017-01, Vol.287 (Pt 1), p.34-43
• Main Authors: Yee, Andrew G., Freestone, Peter S., Bai, Ji-Zhong, Lipski, Janusz
• Format: Article
• Language: English
• Subjects: Action Potentials - drug effects; Animals; Animals, Newborn; Antihypertensive Agents - pharmacology; Brain slice; Calcium; Calcium - metabolism; Diazoxide - pharmacology; Electrochemistry; Electrophysiology; Hydrogen Peroxide - metabolism; Hypoglycemic Agents - pharmacology; In Vitro Techniques; Insecticides - pharmacology; KATP; Locus Coeruleus - cytology; Membrane Potential, Mitochondrial - drug effects; Neurons - classification; Neurons - drug effects; Parkinsonian toxin; Pars Compacta - cytology; Patch-Clamp Techniques; Rats; Rats, Wistar; Reactive Oxygen Species - metabolism; Rotenone - pharmacology; Tolbutamide - pharmacology; TRPM Cation Channels - metabolism; TRPM2
• ISSN: 0014-4886; 1090-2430
• DOI: 10.1016/j.expneurol.2016.10.010

Parkinson's disease (PD) is not only associated with degeneration of dopaminergic (DAergic) neurons in the Substantia Nigra, but also with profound loss of noradrenergic neurons in the Locus Coeruleus (LC). Remarkably, LC degeneration may exceed, or even precede the loss of nigral DAergic neurons, suggesting that LC neurons may be more susceptible to damage by various insults. Using a combination of electrophysiology, fluorescence imaging and electrochemistry, we directly compared the responses of LC, nigral DAergic and nigral non-dopaminergic (non-DAergic) neurons in rat brain slices to acute application of rotenone, a mitochondrial toxin used to create animal and in vitro models of PD. Rotenone (0.01–5.0μM) dose-dependently inhibited the firing of all three groups of neurons, primarily by activating KATP channels. The toxin also depolarised mitochondrial potential (Ψm) and released reactive oxygen species (H2O2). When KATP channels were blocked, rotenone (1μM) increased the firing of LC neurons by activating an inward current associated with dose-dependent increase of cytosolic free Ca2+ ([Ca2+]i). This effect was attenuated by blocking oxidative stress-sensitive TRPM2 channels, and by pre-treatment of slices with anti-oxidants. These results demonstrate that rotenone inhibits the activity of LC neurons mainly by activating KATP channels, and increases [Ca2+]ivia TRPM2 channels. Since the responses of LC neurons were smaller than those of nigral DAergic neurons, our study shows that LC neurons are paradoxically less sensitive to acute effects of this parkinsonian toxin. [Display omitted] •Rotenone inhibited the firing of NAergic LC neurons by activating KATP channels.•The toxin also increased intracellular Ca2+ by activating TRPM2 channels.•Rotenone depolarised mitochondria and released H2O2 from these neurons.•Responses of LC neurons were compared to nigral DAergic and non-DAergic neurons.•LC neurons were less sensitive than nigral DAergic neurons to effects of rotenone.