SwePub
Sök i LIBRIS databas

  Utökad sökning

id:"swepub:oai:DiVA.org:uu-426301"
 

Sökning: id:"swepub:oai:DiVA.org:uu-426301" > Enhanced neprilysin...

Enhanced neprilysin-mediated degradation of hippocampal A beta 42 with a somatostatin peptide that enters the brain

Rofo, Fadi (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Yilmaz, Canan Ugur (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Metzendorf, Nicole G., 1979- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
visa fler...
Gustavsson, Tobias (författare)
Uppsala universitet,Geriatrik
Beretta, Chiara (författare)
Uppsala universitet,Geriatrik
Erlandsson, Anna (författare)
Uppsala universitet,Geriatrik
Sehlin, Dag, 1976- (författare)
Uppsala universitet,Geriatrik
Syvänen, Stina (författare)
Uppsala universitet,Geriatrik
Nilsson, Per (författare)
Karolinska Inst, Dept Neurobiol Care Sci & Soc, Stockholm, Sweden.
Hultqvist, Greta, 1980- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Protein drug design
visa färre...
 (creator_code:org_t)
IVYSPRING INT PUBL, 2021
2021
Engelska.
Ingår i: Theranostics. - : IVYSPRING INT PUBL. - 1838-7640. ; 11:2, s. 789-804
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: Aggregation of the amyloid-beta (A beta) peptide is one of the main neuropathological events in Alzheimer's disease (AD). Neprilysin is the major enzyme degrading A beta, with its activity enhanced by the neuropeptide somatostatin (SST). SST levels are decreased in the brains of AD patients. The poor delivery of SST over the blood-brain barrier (BBB) and its extremely short half-life of only 3 min limit its therapeutic significance.Methods: We recombinantly fused SST to a BBB transporter binding to the transferrin receptor. Using primary neuronal cultures and neuroblastoma cell lines, the ability of the formed fusion protein to activate neprilysin was studied. SST-scFv8D3 was administered to mice overexpressing the A beta-precursor protein (A beta PP) with the Swedish mutation (APPswe) as a single injection or as a course of three injections over a 72 h period. Levels of neprilysin and A beta were quantified using an Enzyme-linked immunosorbent assay (ELISA). Distribution of SST-scFv8D3 in the brain, blood and peripheral organs was studied by radiolabeling with iodine-125.Results: The construct, SST-scFv8D3, exhibited 120 times longer half-life than SST alone, reached the brain in high amounts when injected intravenously and significantly increased the brain concentration of neprilysin in APPswe mice. A significant decrease in the levels of membrane-bound A beta 42 was detected in the hippocampus and the adjacent cortical area after only three injections.Conclusion: With intravenous injections of our BBB permeable SST peptide, we were able to significantly increase the levels neprilysin, an effect that was followed by a significant and selective degradation of membrane-bound A beta 42 in the hippocampus. Being that membrane-bound A beta triggers neuronal toxicity and the hippocampus is the central brain area in the progression of AD, the study has illuminated a new potential treatment paradigm with a promising safety profile targeting only the disease affected areas.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Nyckelord

Amyloid-beta (A beta)
blood-brain barrier (BBB)
neprilysin
somatostatin (SST)
transferrin receptor (TfR)

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy