Synaptic Plasticity in the CA1 Area of the Hippocampus of Scrapie-Infected Mice

Using conventionalin vitroextracellular field potential recordings we have investigated both short- and long-term synaptic plasticity in the hippocampal CA1 area of mice infected with ME7 scrapie. In agreement with earlier studies, no changes were seen in the properties of the Schäffer collateral-ev...

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Main Authors: Alex R. Johnston, Janet R. Fraser, Martin Jeffrey, Nikki MacLeod
Format: Article
Language:English
Published: Elsevier 1998-09-01
Series:Neurobiology of Disease
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996198901942
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spelling doaj-a12c9ebaf504404e823508768b0947582021-03-22T08:43:31ZengElsevierNeurobiology of Disease1095-953X1998-09-0153188195Synaptic Plasticity in the CA1 Area of the Hippocampus of Scrapie-Infected MiceAlex R. Johnston0Janet R. Fraser1Martin Jeffrey2Nikki MacLeod3Department of Physiology, University Medical School, Teviot Place, Edinburgh, EH8 9AG, United Kingdom; BBSRC and MRC Neuropathogenesis Unit, Institute of Animal Health, Kings Buildings, West Mains Road, Edinburgh, EH9 3JQ, United Kingdom; Lasswade Veterinary Laboratory, Bush Estate, Penicuick, Midlothian, EH26 OSA, United KingdomDepartment of Physiology, University Medical School, Teviot Place, Edinburgh, EH8 9AG, United Kingdom; BBSRC and MRC Neuropathogenesis Unit, Institute of Animal Health, Kings Buildings, West Mains Road, Edinburgh, EH9 3JQ, United Kingdom; Lasswade Veterinary Laboratory, Bush Estate, Penicuick, Midlothian, EH26 OSA, United KingdomDepartment of Physiology, University Medical School, Teviot Place, Edinburgh, EH8 9AG, United Kingdom; BBSRC and MRC Neuropathogenesis Unit, Institute of Animal Health, Kings Buildings, West Mains Road, Edinburgh, EH9 3JQ, United Kingdom; Lasswade Veterinary Laboratory, Bush Estate, Penicuick, Midlothian, EH26 OSA, United KingdomDepartment of Physiology, University Medical School, Teviot Place, Edinburgh, EH8 9AG, United Kingdom; BBSRC and MRC Neuropathogenesis Unit, Institute of Animal Health, Kings Buildings, West Mains Road, Edinburgh, EH9 3JQ, United Kingdom; Lasswade Veterinary Laboratory, Bush Estate, Penicuick, Midlothian, EH26 OSA, United KingdomUsing conventionalin vitroextracellular field potential recordings we have investigated both short- and long-term synaptic plasticity in the hippocampal CA1 area of mice infected with ME7 scrapie. In agreement with earlier studies, no changes were seen in the properties of the Schäffer collateral-evoked field excitatory postsynaptic potential during the early stages of the disease (up to 160 days, post inoculation, d.p.i) after which time the recorded potentials were seen to attenuate. Also, up to this time no changes were seen in either paired-pulse facilitation or post-tetanic potentiation, which are short-term phenomena associated with brief elevations in presynaptic calcium levels. However, there was a significant shift from the ability of slices to maintain long-term potentiation (LTP) from 100 d.p.i. onwards. In all of these experiments short-term potentiation (STP) was preserved, suggesting that from the time that abnormal PrP becomes detectable, or perhaps even earlier, the mechanisms responsible for stabilizing the maintenance phase of LTP are impaired. This result is discussed in terms of the relationship between STP and LTP and how this might be compromised by the conversion of cellular prion protein (PrPC) to the scrapie, protease resistant form of PrP (PrPSc).http://www.sciencedirect.com/science/article/pii/S0969996198901942scrapieprionelectrophysiologylong-term potentiationhippocampusbrain slice
collection DOAJ
language English
format Article
sources DOAJ
author Alex R. Johnston
Janet R. Fraser
Martin Jeffrey
Nikki MacLeod
spellingShingle Alex R. Johnston
Janet R. Fraser
Martin Jeffrey
Nikki MacLeod
Synaptic Plasticity in the CA1 Area of the Hippocampus of Scrapie-Infected Mice
Neurobiology of Disease
scrapie
prion
electrophysiology
long-term potentiation
hippocampus
brain slice
author_facet Alex R. Johnston
Janet R. Fraser
Martin Jeffrey
Nikki MacLeod
author_sort Alex R. Johnston
title Synaptic Plasticity in the CA1 Area of the Hippocampus of Scrapie-Infected Mice
title_short Synaptic Plasticity in the CA1 Area of the Hippocampus of Scrapie-Infected Mice
title_full Synaptic Plasticity in the CA1 Area of the Hippocampus of Scrapie-Infected Mice
title_fullStr Synaptic Plasticity in the CA1 Area of the Hippocampus of Scrapie-Infected Mice
title_full_unstemmed Synaptic Plasticity in the CA1 Area of the Hippocampus of Scrapie-Infected Mice
title_sort synaptic plasticity in the ca1 area of the hippocampus of scrapie-infected mice
publisher Elsevier
series Neurobiology of Disease
issn 1095-953X
publishDate 1998-09-01
description Using conventionalin vitroextracellular field potential recordings we have investigated both short- and long-term synaptic plasticity in the hippocampal CA1 area of mice infected with ME7 scrapie. In agreement with earlier studies, no changes were seen in the properties of the Schäffer collateral-evoked field excitatory postsynaptic potential during the early stages of the disease (up to 160 days, post inoculation, d.p.i) after which time the recorded potentials were seen to attenuate. Also, up to this time no changes were seen in either paired-pulse facilitation or post-tetanic potentiation, which are short-term phenomena associated with brief elevations in presynaptic calcium levels. However, there was a significant shift from the ability of slices to maintain long-term potentiation (LTP) from 100 d.p.i. onwards. In all of these experiments short-term potentiation (STP) was preserved, suggesting that from the time that abnormal PrP becomes detectable, or perhaps even earlier, the mechanisms responsible for stabilizing the maintenance phase of LTP are impaired. This result is discussed in terms of the relationship between STP and LTP and how this might be compromised by the conversion of cellular prion protein (PrPC) to the scrapie, protease resistant form of PrP (PrPSc).
topic scrapie
prion
electrophysiology
long-term potentiation
hippocampus
brain slice
url http://www.sciencedirect.com/science/article/pii/S0969996198901942
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