PLoS ONE · 2012 · 55 citations · 37 references
Life SciencesNeurosciencePharmacologyDementiaMolecular NeuroscienceNeurodegenerationAlzheimer DiseaseAmyloid FormationMicroglia BiologyNeurodegeneration MechanismsNeurodegenerative DiseasesNeurodegenerative DisordersAmyloid Beta PeptidesAmyloid Beta PlaquesAmyloid Plaque FormationAmyloid PlaquesOctreotide TherapyProteolytic ActivityProteolytic Enzyme ActivityTherapeutic Targeting Of Amyloid
The deposition of β-amyloid (Aβ) into senile plaques and the impairment of somatostatin-mediated neurotransmission are key pathological events in the onset of Alzheimer's disease (AD). Insulin-degrading-enzyme (IDE) is one of the main extracellular protease targeting Aβ, and thus it represents an interesting pharmacological target for AD therapy. We show that the active form of somatostatin-14 regulates IDE activity by affecting its expression and secretion in microglia cells. A similar effect can also be observed when adding octreotide. Following a previous observation where somatostatin directly interacts with IDE, here we demonstrate that somatostatin regulates Aβ catabolism by modulating IDE proteolytic activity in IDE gene-silencing experiments. As a whole, these data indicate the relevant role played by somatostatin and, potentially, by analogue octreotide, in preventing Aβ accumulation by partially restoring IDE activity.
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SMS 201–995: A very potent and selective octapeptide analogue of somatostatin with prolonged action
W. Bauer, U. Briner, W. Doepfner et al. · Life Sciences · 1982 · 1.3K citations