Literature DB >> 8981616

Metrifonate treatment enhances acquisition of eyeblink conditioning in aging rabbits.

M A Kronforst-Collins1, P L Moriearty, M Ralph, R E Becker, B Schmidt, L T Thompson, J F Disterhoft.   

Abstract

The cholinergic system is known to show deterioration during aging and Alzheimer's disease. In response, a therapeutic approach to Alzheimer's disease has been to attempt to compensate for the decrease in central cholinergic function by potentiating the activity of the remaining intact cholinergic cells with cholinesterase inhibitors. In this study treatment with the long-lasting cholinesterase inhibitor metrifonate enhanced acquisition of eyeblink conditioning in aging rabbits without producing interfering side effects. The effects of metrifonate on central and peripheral cholinesterase activity were evaluated, as was the involvement of plasma atropine esterase activity on the central and peripheral response to metrifonate. Results demonstrate that metrifonate can produce predictable, dose-dependent ChE inhibition. Associative learning in the aging rabbit was improved by metrifonate-induced steady state ChE inhibition within a range of 30-80%. Metrifonate was behaviorally effective in the absence of the severe side effects which typically plague cholinesterase inhibitors, suggesting that metrifonate is a possible treatment for the cognitive deficits resulting from normal aging and Alzheimer's disease.

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Year:  1997        PMID: 8981616     DOI: 10.1016/S0091-3057(96)00164-5

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  12 in total

Review 1.  Physiological and anatomical studies of associative learning: Convergence with learning studies of W.T. Greenough.

Authors:  Roberto Galvez; Daniel A Nicholson; John F Disterhoft
Journal:  Dev Psychobiol       Date:  2011-07       Impact factor: 3.038

2.  Kinetics of brain cholinesterase inhibition following metrifonate administration.

Authors:  S Dachir; B H Schmidt; A Levy
Journal:  Neurochem Res       Date:  1999-08       Impact factor: 3.996

3.  Ovarian hormone deficiency reduces intrinsic excitability and abolishes acute estrogen sensitivity in hippocampal CA1 pyramidal neurons.

Authors:  Wendy W Wu; John P Adelman; James Maylie
Journal:  J Neurosci       Date:  2011-02-16       Impact factor: 6.167

4.  Metrifonate increases neuronal excitability in CA1 pyramidal neurons from both young and aging rabbit hippocampus.

Authors:  M M Oh; J M Power; L T Thompson; P L Moriearty; J F Disterhoft
Journal:  J Neurosci       Date:  1999-03-01       Impact factor: 6.167

5.  Mechanisms underlying basal and learning-related intrinsic excitability in a mouse model of Alzheimer's disease.

Authors:  C C Kaczorowski; E Sametsky; S Shah; R Vassar; J F Disterhoft
Journal:  Neurobiol Aging       Date:  2009-10-14       Impact factor: 4.673

6.  Cellular mechanisms for altered learning in aging.

Authors:  M Matthew Oh; John F Disterhoft
Journal:  Future Neurol       Date:  2010-01-01

7.  AR-R 17779 improves social recognition in rats by activation of nicotinic alpha7 receptors.

Authors:  Marja Van Kampen; Karin Selbach; Renate Schneider; Elleonore Schiegel; Frank Boess; Rudy Schreiber
Journal:  Psychopharmacology (Berl)       Date:  2004-01-15       Impact factor: 4.530

8.  Effects of subchronic administration of metrifonate on cholinergic neurotransmission in rats.

Authors:  V C Hinz; J Kolb; B H Schmidt
Journal:  Neurochem Res       Date:  1998-07       Impact factor: 3.996

9.  Galantamine facilitates acquisition of hippocampus-dependent trace eyeblink conditioning in aged rabbits.

Authors:  Aldis P Weible; M Matthew Oh; Grace Lee; John F Disterhoft
Journal:  Learn Mem       Date:  2004 Jan-Feb       Impact factor: 2.460

Review 10.  Learning and aging affect neuronal excitability and learning.

Authors:  M Matthew Oh; John F Disterhoft
Journal:  Neurobiol Learn Mem       Date:  2019-11-28       Impact factor: 2.877

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