I. Llano et Hm. Gerschenfeld, BETA-ADRENERGIC ENHANCEMENT OF INHIBITORY SYNAPTIC ACTIVITY IN RAT CEREBELLAR STELLATE AND PURKINJE-CELLS, Journal of physiology, 468, 1993, pp. 201-224
1. Using the tight-seal whole-cell recording technique. we studied the
effects of noradrenaline (NA) on the spontaneous inhibitory synaptic
currents (IPSCs) of stellate and Purkinje cells in rat cerebellar slic
es. 2. In both types of cells, NA (10 muM) induced a marked increase i
n the frequency of the IPSCs. This effect was observed both in the abs
ence and in the presence of TTX in the saline bathing the cerebellar s
lices. 3. The NA-induced increase in frequency of IPSCs and miniature
IPSCs (mIPSCs) in the two cell types was mimicked by bath applications
of isoprenaline (10 muM) and of the adenylyl cyclase activator forsko
lin (20 muM). Neither phenylephrine nor clonidine changed the frequenc
y of IPSCs in stellate or Purkinje cells. 4. ln stellate cells, the be
ta-agonists and forskolin had variable effects on the amplitudes of bo
th IPSCs and mIPSCs. None of these compounds altered the amplitude of
mIPSCs in Purkinje cells. 5. The responses to local applications of GA
BA to Purkinje cells were unchanged by bath applications of beta-adren
ergic agonists or forskolin. A decrease in the response to GABA after
treatment with these agents was observed in half the stellate cells ex
amined. 6. We conclude that the major effect of NA on stellate and Pur
kinje cells is an increase in the frequency of occurrence of spontaneo
us inhibitory synaptic currents. This action is exerted through the ac
tivation of beta-adrenergic receptors and is probably mediated by an i
ntracellular mechanism involving cAMP. The beta-adrenergic modulation
of IPSC frequency takes place at the presynaptic level and may involve
a change in the process of transmitter release.