Different α2 adrenoceptor subtypes control noradrenaline release and cell firing in the locus coeruleus of wildtype and monoamine oxidase‐A knockout mice

Abstract In this study, we investigated which subtype(s) of α 2 ‐adrenoceptor control stimulated noradrenaline (NA) release and noradrenergic cell firing in the locus coeruleus (LC) of monoamine oxidase‐A knockout (MAO‐A KO) and C3H/HeJ wildtype mice. On short stimulus trains (10 pulses, 200 Hz), the α 2 agonist dexmedetomidine (10 n m ) reduced NA efflux by 78 ± 8% and 51 ± 8% in wildtype and MAO‐A KO mice, respectively. In both strains, BRL 44408 (100 n m ) and ARC 239 (100 n m ) each partially blocked the effect of dexmedetomidine. In MAO‐A KO mice, BRL 44408 (100 n m ) increased evoked NA efflux on short trains while ARC 239 (100 n m ) had no effect. The two antagonists in combination increased NA efflux (by 81 ± 34%, P < 0.001), significantly more than by BRL 44408 alone. Conversely, in wildtype mice, the α 2 ‐adrenoceptor antagonists did not significantly increase LC NA efflux. On long stimuli (30 pulses, 10 Hz), NA efflux was increased by BRL 44408 ( P < 0.001) but not by ARC 239. The effect of BRL 44408 was significantly greater in MAO‐A KO than wildtype mice (208 ± 43% vs. 113 ± 31% increase, P < 0.001). When we examined noradrenergic cell firing, we found that dexmedetomidine inhibited LC cell firing in both strains with comparable EC 50 values (2–5 n m ), although E max was significantly lower in MAO‐A KO mice ( P < 0.001). The agonist effect was antagonized by BRL 44408 ( P < 0.001) in wildtype but not in MAO‐A KO mice, with a p K B of 7.75. ARC 239 had no effect on the agonist response in either strain. A combination of the antagonists was no more effective than BRL 44408 alone (in wildtypes) and had no effect in MAO‐A KO mice. Neither BRL 44408 nor ARC 239 affected basal LC cell firing in wildtype or MAO‐A KO mice. Collectively, these results suggest that, analogous to other monoamine cell groups, there are differences in the autoreceptor populations controlling NA efflux and LC cell firing and that important differences exist between MAO‐A KO and wildtype mice