Ih blockade reduces cocaine-induced firing patterns of putative dopaminergic neurons of the ventral tegmental area in the anesthetized rat

Karl Y. Bosque-Cordero, Rafael Vazquez-Torres, Cristhian Calo-Guadalupe, Daisy Consuegra-Garcia, Giulia R. Fois, François Georges, Carlos A. Jimenez-Rivera
Progress in Neuro-Psychopharmacology and Biological Psychiatry. 2022-01-01; 112: 110431
DOI: 10.1016/j.pnpbp.2021.110431

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Bosque-Cordero KY(1), Vazquez-Torres R(2), Calo-Guadalupe C(2), Consuegra-Garcia D(2), Fois GR(3), Georges F(3), Jimenez-Rivera CA(4).

Author information:
(1)University of Puerto Rico Rio Piedras Campus, San Juan, Puerto Rico.
(2)University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico.
(3)University of Bordeaux, Neurodegeneratives Diseases Institute, IMN-UMR-CNRS 5293, 146 rue Léo Saignat, 33076 Bordeaux, France; CNRS, Neurodegeneratives Diseases Institute, IMN-UMR-CNRS 5293, 146 rue Léo Saignat, 33076 Bordeaux, France.
(4)University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico. Electronic address: .

The hyperpolarization-activated cation current (Ih) is a determinant of intrinsic excitability in various cells, including dopaminergic neurons (DA) of the ventral tegmental area (VTA). In contrast to other cellular conductances, Ih is activated by hyperpolarization negative to -55 mV and activating Ih produces a time-dependent depolarizing current. Our laboratory demonstrated that cocaine sensitization, a chronic cocaine behavioral model, significantly reduces Ih amplitude in VTA DA neurons. Despite this reduction in Ih, the spontaneous firing of VTA DA cells after cocaine sensitization remained similar to control groups. Although the role of Ih in controlling VTA DA excitability is still poorly understood, our hypothesis is that Ih reduction could play a role of a homeostatic controller compensating for cocaine-induced change in excitability. Using in vivo single-unit extracellular electrophysiology in isoflurane
anesthetized rats, we explored the contribution of Ih on spontaneous firing patterns of VTA DA neurons. A key feature of spontaneous excitability is bursting activity; bursting is defined as trains of two or more spikes occurring within a
short interval and followed by a prolonged period of inactivity. Burst activity increases the reliability of information transfer. To elucidate the contribution of Ih to spontaneous firing patterns of VTA DA neurons, we locally infused an Ih
blocker (ZD 7288, 8.3 μM) and evaluated its effect. Ih blockade significantly reduced firing rate, bursting frequency, and percent of spikes within a burst. In addition, Ih blockade significantly reduced acute cocaine-induced spontaneous
firing rate, bursting frequency, and percent of spikes within a burst. Using whole-cell patch-clamp, we determine the progressive reduction of Ih after acute and chronic cocaine administration (15 mg/k.g intraperitoneally). Our data show a significant reduction (~25%) in Ih amplitude after 24 but not 2 h of acute cocaine administration. These results suggest that a progressive reduction of Ih could serve as a homeostatic regulator of cocaine-induced spontaneous firing patterns related to VTA DA excitability.

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Auteurs Bordeaux Neurocampus