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Biomedical subjects

J S Kelly

Publications and source records attributed to J S Kelly.

At least 109 records · Page 6Linked to original sources

The actions of cholecystokinin and related peptides on pyramidal neurones of the mammalian hippocampus.

The presence of cholecystokinin octapeptide (CCK-8) immunoreactivity in the vicinity of the pyramidal neurones of the mammalian hippocampus has allowed us to investigate the central postsynaptic actions of CCK-8 and a number of related peptides, at a site thought to be innervated by a peptidergic pathway. Intracellular records from pyramidal cells of the CA1 region of the hippocampal slice preparation were used to determine changes in excitability and associated changes in membrane potential and resistance evoked by the pressure application of peptides into the cell body layer, from an independently mounted multibarrelled micropipette. The tetra- and octa-peptide C-terminal fragments of cholecystokinin evoked abrupt and rapidly reversible depolarizations which were accompanied by marked increases in excitability and a decrease in membrane input resistance. A comparison was made of the actions of these peptides with those of glutamate, released by iontophoresis from an adjacent barrel of the same multibarrelled pipette. The rate of onset of the cholecystokinin-evoked response was similar to that of the response evoked by glutamate. C-terminal fragments of gastrin (G-13 and G-14) and bombesin were also found to be excitatory to pyramidal neurones in the CA1 region. However, the nonsulphated form of CCK-8 was inactive, as was substance P, a peptide not present in the hippocampus.

Animals↗

Action of 5-hydroxytryptamine on granule cells in the rat hippocampal slice.

1. The action of iontophoretic applications of 5HT on granule cells of the dentate gyrus was studied in the rat hippocampal slice with intracellular electrodes. 2. The inhibition produced by 5HT was accompanied by a depolarization of the membrane and a substantial decrease in input resistance. 3. 5HT was only inhibitory when applied close to the soma and had no effect when applied to the dendritic region of the cell. 4. The reversal potential for the 5HT response was estimated to be 15.5 +/- 6 mV depolarizing with respect to resting membrane potential; increasing intracellular Cl- shifted the reversal potential to a more positive value. 5. Equipotent applications of GABA applied from adjacent barrels of the same multibarrel electrode evoked similar responses with an identical equilibrium potential.

Animals↗

Lack of labelling of microglial cells following microinjection of [3H] beta-alanine: an electron microscopic autoradiographic study.

Following axotomy of the facial nerve, the uptake of [3H] beta-alanine into different types of glial cells in the facial nucleus was studied by autoradiography. A marked proliferation of microglial cells, predominantly in a satellite position to neurons, was accompanied by a localization of [3H] beta--alanine over astrocytes and oligodendrocytes but not over microglial cells. Microglial cells therefore appear to be a functionally distinct cell type and should not be classified with the macroglia.

Alanine↗