Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0022116 (
ischemia
)
91,303
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Carboxypeptidase E, an exoprotease involved in the processing of bioactive peptides released by a regulated secretory pathway, was identified in a subtractive complementary DNA library derived from an ischemic rat brain by differential screening. In situ hybridization and immunocytochemical analysis showed the presence of
carboxypeptidase E
messenger RNA and protein in the cerebral cortex, thalamus, striatum, and hippocampus of a healthy rat brain. After 15 minutes of transient global
ischemia
followed by 8 hours of reperfusion, increased levels of
carboxypeptidase E
messenger RNA and protein were observed in the hippocampal CA1 and CA3 regions and in the cortex, as detected by Northern and Western blot analyses and in situ hybridization. After extended reperfusion (24 to 72 hours), both
carboxypeptidase E
messenger RNA and protein levels were decreased. The
ischemia
-induced changes in
carboxypeptidase E
expression suggest that this enzyme may play a role in modulating the brain's response to
ischemia
.
...
PMID:Altered expression of the neuropeptide-processing enzyme carboxypeptidase E in the rat brain after global ischemia. 1174 Feb 3
In this study, using both in vivo and in vitro
ischemia
models, the authors investigated the impact of brain
ischemia
on the biosynthesis of a key neuropeptide-processing enzyme,
carboxypeptidase E
(
CPE
). The response to brain
ischemia
of animals that lacked an active
CPE
was also examined. Combined in situ hybridization and immunocytochemical analyses for
CPE
showed reciprocal changes of
CPE
mRNA and protein, respectively, in the same cortical cells in rat brains after focal cerebral ischemia. Western blot analysis revealed an accumulation of the precursor protein of
CPE
in the ischemic cortex in vivo and in ischemic cortical neurons in vitro. Detailed metabolic labeling experiments on ischemic cortical neurons showed that ischemic stress caused a blockade in the proteolytic processing of
CPE
. When mice lacking an active
CPE
protease were subjected to a sublethal episode of focal cerebral ischemia, abundant TUNEL-positive cells were seen in the ischemic cortex whereas only a few were seen in the cortex of wild-type animals. These findings suggest that
ischemia
has an adverse impact on the neuropeptide-processing system in the brain and that the lack of an active neuropeptide-processing enzyme exacerbates ischemic brain injury.
...
PMID:Altered biosynthesis of neuropeptide processing enzyme carboxypeptidase E after brain ischemia: molecular mechanism and implication. 1518 68