Neurochemical characterization of the striatum and the nucleus accumbens in L-type Ca(v)1.3 channels knockout mice

• Published in: Neurochemistry international Vol. 60; no. 3; pp. 229 - 232
• Main Authors: Sagala, Ferry S P, Harnack, Daniel, Bobrov, Evgeny, Sohr, Reinhard, Gertler, Christoph, James Surmeier, D, Kupsch, Andreas
• Format: Journal Article
• Language: English
• Published: England 01.02.2012
• Subjects: Animals; Calcium Channels, L-Type - genetics; Calcium Channels, L-Type - physiology; Chromatography, High Pressure Liquid; Corpus Striatum - metabolism; DNA - biosynthesis; DNA - genetics; Dopamine - metabolism; Female; gamma-Aminobutyric Acid - metabolism; Glutamic Acid - metabolism; Male; Mice; Mice, Knockout; Nucleus Accumbens - metabolism; Real-Time Polymerase Chain Reaction; Serotonin - metabolism; Taurine - metabolism; Ventral Tegmental Area - drug effects; Ventral Tegmental Area - metabolism
• ISSN: 1872-9754
• DOI: 10.1016/j.neuint.2011.12.009

L-type Ca(v)1.3 channels control the autonomous pacemaking of the substantia nigra (SN) dopamine (DA) neurons, which maintains the sustained release of DA in the striatum, its target structure. The persistent engagement of L-type channels during pacemaking might lead to increased vulnerability to environmental stressors or degenerative processes, providing a mechanism for the development of Parkinson's disease (PD). Interestingly, L-type channels are not necessary for pacemaking, opening the possible use of calcium channel antagonists as neuroprotective agents for PD without disturbing normal DA function. In this study we aimed to evaluate the consequences of Ca(v)1.3 channels deletion at the neurochemical level. For this purpose, tissue concentrations of DA and their respective metabolites were measured using high performance liquid chromatography (HPLC) in the striatum and the nucleus accumbens (NAcc) of mice lacking the gene for the Ca(v)1.3 channel subunit (CACNA1D) and compared to those in wild-type mice. Striatal DA level did not differ between the two groups. In contrast, the level of serotonin, glutamate, GABA, and taurine were increased by more than 50% in the striatum of Ca(v)1.3 null mice. Neurotransmitters levels in the NAcc did not differ between the different groups. In conclusion, our results neurochemically corroborate the robustness of the nigrostriatal DA neurons in the absence of Ca(v)1.3 channels, but suggest that complete deletion of this channel affected a variety of other transmitter systems.