Immunological detection of glutamate receptor subtypes in human central nervous system
β Scribed by Craig D. Blackstone; Allan I. Levey; Lee J. Martin; Donald L. Price; Dr Richard L. Huganir
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 661 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
β¦ Synopsis
Glutamate receptors are the principal excitatory neurotransmitter receptors in the central nervous system and are involved in a number of normal and pathological neuronal processes. Using subunit-specific antipeptide antibodies developed against the predicted amino acid sequences of several rat glutamate receptor cDNAs, we have identified these proteins in post-mortem human central nervous system tissue. Immunoblotting of dissected brain regions demonstrates that these receptor proteins are differentially distributed. The ability to identify these proteins in post-mortem human tissues should allow examination of the changes in levels of receptor subtypes that occur in a variety of neurological and psychiatric diseases.
π SIMILAR VOLUMES
Previous physiological and pharmacological evidence has suggested a neurotransmitter role for the excitatory amino acid glutamate in the leech central nervous system (CNS). In the present study, we sought to localize glutamate receptor (GluR) subunits (GluR 5/6/7, GluR 2/3 and N-methyl-D-aspartate r
## Abstract Previous studies on glutamate (GLU) and its receptors in the pond snail __Lymnaea stagnalis__ have suggested that GLU functions as a neurotransmitter in various behaviors, particularly for generation of feeding rhythm. The uptake mechanism of GLU is not yet known in __Lymnaea__. In the
g-Aminobutyric acid (GABA) is the main inhibitory neurotransmitter in the cockroach central nervous system (CNS). Electrophysiological assays performed at cercal-afferent giant-interneuron (GI) synapses demonstrated that a biphasic (transient and stable phases) increase in membrane conductance, in r
The ability of microglia to migrate through central nervous system (CNS) tissue requires proteolytic degradation of components of the extracellular matrix. Urokinase plasminogen activator (uPA), when bound to its cell surface receptor (uPAR), is an active cell surface protease. uPAR expression has b