Comparing adenosine A2A receptor modulation of cannabinoid CB1 receptor-mediated inhibition of GABA and glutamate release in rodent striatal nerve terminals

被引:0
|
作者
Ferreira, Samira G. [1 ,2 ]
Bitencourt, Rafael M. [1 ,3 ]
Garcao, Pedro [1 ,4 ]
Cunha, Rodrigo A. [1 ,2 ,5 ]
Kofalvi, Attila [1 ,2 ]
机构
[1] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, Coimbra, Portugal
[2] Univ Coimbra, Ctr Innovat Biomed & Biotechnol CIBB, P-3000548 Coimbra, Portugal
[3] Univ South Santa Catarina, Postgrad Program Hlth Sci, Tubarao, Brazil
[4] Talisman Therapeut, Jonas Webb Bldg,Babraham Res Campus, Cambridge, England
[5] Univ Coimbra, Fac Med, Coimbra, Portugal
关键词
A(2A) receptor; CB1; receptor; GABA; glutamate; GPCR heteromerization; striatum; PURINERGIC MODULATION; SYNAPTIC MODULATION; PLASTICITY; TRANSMISSION; NEURONS; ROLES; ACID; ENDOCANNABINOIDS; IDENTIFICATION; STIMULATION;
D O I
10.1111/ejn.16642
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In corticostriatal nerve terminals, glutamate release is stimulated by adenosine via A(2A) receptors (A(2A)Rs) and simultaneously inhibited by endocannabinoids via CB1 receptors (CB(1)Rs). We previously identified presynaptic A(2A)R-CB1R heterotetrameric complexes in corticostriatal nerve terminals. We now explored the possible functional interaction between A(2A)Rs and CB(1)Rs in purified striatal GABAergic nerve terminals (synaptosomes) and compared these findings with those on the release of glutamate. In the striatal synaptosomes of rats and wild-type mice, the synthetic cannabinoid receptor agonist WIN55212-2 (10-1000 nM) attenuated the Ca2+-dependent, high-K+-evoked release of gamma-[2,3-H-3(N)]-aminobutyric acid ([H-3]GABA) and [H-3]glutamate. WIN55212-2 did not affect the evoked release of either neurotransmitter under CB1R blockade by AM251 or O-2050 or in CB1R knockout (KO) mice. The A(2A)R-selective agonist CGS21680 (30 nM) and the A(2A)R-selective antagonist SCH58261 (100 nM) dampened the inhibitory action of WIN55212-2 in rat synaptosomes. Another A(2A)R-selective antagonist, ZM241385 (100 nM), abolished the inhibition by WIN55212-2 of the evoked release of both [H-3]GABA and [H-3]glutamate. Surprisingly, WIN55212-2 also failed to inhibit the evoked release of [H-3]GABA but not of [H-3]glutamate in A(2A)R KO mice of both CD-1 and C57BL/6 strains. In rat striatal synaptosomal membranes, the binding of [H-3]ZM241385 to A(2A)Rs was not affected by cannabinoids. However, ZM241385 reduced the B-max while CGS21680 and SCH58261 increased the K-D of [H-3]SR141716A binding to CB1R, indicating an A(2A)R-ligand-specific modulation of CB1R function. CB1R B-max and K-D were reduced in A(2A)R KO mice, whereas A(2A)R B-max was smaller in CB1R KO mice. Altogether, our data reveal an intricate interdependence of presynaptic A(2A)Rs and CB(1)Rs on striatal neuromodulation.
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页数:17
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