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Intracellular recordings from the paraventricular nucleus in slices of rat hypothalamus.
Author(s) -
Dudek F E,
Hatton G I,
Macvicar B A
Publication year - 1980
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1980.sp013192
Subject(s) - antidromic , orthodromic , depolarization , neuroscience , excitatory postsynaptic potential , stimulation , extracellular , chemistry , electrophysiology , hypothalamus , slice preparation , biophysics , biology , inhibitory postsynaptic potential , biochemistry
1. The electrical activity of thirty‐five neurones in the lateral area of the paraventricular nucleus (p.v.n.) was recorded intracellularly in vitro from slices of rat hypothalamus. 2. Spontaneously occurring action potentials were observed in twenty‐four of the neurones. The temporal pattern of action potentials was generally slow and irregular; occasionally some cells fired bursts of action potentials. 3. Depolarizations with a fast rising phase and slow decay occurred spontaneously in most cells. These depolarizations exhibited a wide range of amplitudes in each cell (up to 33 mV), showed temporal summation, and could serve as pre‐potentials for spontaneously occurring action potentials. Presumably, these depolarizations were excitatory post‐synaptic potentials (e.p.s.p.s.). 4. Depolarizing current injection could evoke action potentials. Extracellular stimuli dorsolateral to the fornix column occasionally elicited action potentials which had a short and invariant latency and which could respond to stimulation rates of 100 Hz. In some cases, extracellular stimuli in the same area evoked depolarizations which had long and variable latency and were similar to those occurring spontaneously. These two types of responses probably represent antidromic and orthodromic activation respectively. 5. Intracellular injections of horseradish peroxidase suggest that these recordings were obtained primarily, but not exclusively, from magnocellular neuroendocrine cells. This is consistent with previous anatomical studies on the location of magnocellular elements in p.v.n.