Matches in SemOpenAlex for { <https://semopenalex.org/work/W2599990538> ?p ?o ?g. }
- W2599990538 endingPage "232" @default.
- W2599990538 startingPage "223" @default.
- W2599990538 abstract "A pressing need exists for long-acting, non-addictive medicines to treat chronic pain, a major societal burden. Botulinum neurotoxin type A (BoNT/A) complex – a potent, specific and prolonged inhibitor of neuro-exocytosis – gives some relief in several pain disorders, but not for all patients. Our study objective was to modify BoNT/A to overcome its inability to block transmitter release elicited by high [Ca2+]i and increase its limited analgesic effects. This was achieved by fusing a BoNT/A gene to that for the light chain (LC) of type/E. The resultant purified protein, LC/E-BoNT/A, entered cultured sensory neurons and, unlike BoNT/A, inhibited release of calcitonin gene-related peptide evoked by capsaicin. Western blotting revealed that this improvement could be due to a more extensive truncation by LC/E of synaptosomal-associated protein of Mr = 25 k, essential for neuro-exocytosis. When tested in a rat spared nerve injury (SNI) model, a single intra-plantar (IPL) injection of LC/E-BoNT/A alleviated for ∼2 weeks mechanical and cold hyper-sensitivities, in a dose-dependent manner. The highest non-paralytic dose (75 U/Kg, IPL) proved significantly more efficacious than BoNT/A (15 U/Kg, IPL) or repeated systemic pregabalin (10 mg/Kg, intraperitoneal), a clinically-used pain modulator. Effects of repeated or delayed injections of this fusion protein highlighted its analgesic potential. Attenuation of mechanical hyperalgesia was extended by a second administration when the effect of the first had diminished. When injected 5 weeks after injury, LC/E-BoNT/A also reversed fully-established mechanical and cold hyper-sensitivity. Thus, combining advantageous features of BoNT/E and/A yields an efficacious, locally-applied and long-acting anti-hyperalgesic." @default.
- W2599990538 created "2017-04-07" @default.
- W2599990538 creator A5018631520 @default.
- W2599990538 creator A5036088530 @default.
- W2599990538 creator A5048987262 @default.
- W2599990538 creator A5052827662 @default.
- W2599990538 creator A5059539564 @default.
- W2599990538 creator A5060061391 @default.
- W2599990538 creator A5060488022 @default.
- W2599990538 creator A5061660173 @default.
- W2599990538 date "2017-05-01" @default.
- W2599990538 modified "2023-10-18" @default.
- W2599990538 title "A novel therapeutic with two SNAP-25 inactivating proteases shows long-lasting anti-hyperalgesic activity in a rat model of neuropathic pain" @default.
- W2599990538 cites W1513245939 @default.
- W2599990538 cites W1519556854 @default.
- W2599990538 cites W1766552324 @default.
- W2599990538 cites W1812574243 @default.
- W2599990538 cites W1847416587 @default.
- W2599990538 cites W1916656475 @default.
- W2599990538 cites W1918151868 @default.
- W2599990538 cites W1964790300 @default.
- W2599990538 cites W1965137822 @default.
- W2599990538 cites W1979246434 @default.
- W2599990538 cites W1993581461 @default.
- W2599990538 cites W1998634781 @default.
- W2599990538 cites W2006048052 @default.
- W2599990538 cites W2006589555 @default.
- W2599990538 cites W2018363788 @default.
- W2599990538 cites W2027063112 @default.
- W2599990538 cites W2033665513 @default.
- W2599990538 cites W2047010161 @default.
- W2599990538 cites W2048223574 @default.
- W2599990538 cites W2056987713 @default.
- W2599990538 cites W2072147078 @default.
- W2599990538 cites W2075715972 @default.
- W2599990538 cites W2076313213 @default.
- W2599990538 cites W2077358692 @default.
- W2599990538 cites W2091149144 @default.
- W2599990538 cites W2097577760 @default.
- W2599990538 cites W2103351070 @default.
- W2599990538 cites W2106246537 @default.
- W2599990538 cites W2113723285 @default.
- W2599990538 cites W2132639205 @default.
- W2599990538 cites W2133093960 @default.
- W2599990538 cites W2147024386 @default.
- W2599990538 cites W2153588448 @default.
- W2599990538 cites W2154507501 @default.
- W2599990538 cites W2154913782 @default.
- W2599990538 cites W2155781531 @default.
- W2599990538 cites W2159842221 @default.
- W2599990538 cites W2159980203 @default.
- W2599990538 cites W2164005268 @default.
- W2599990538 cites W2167613032 @default.
- W2599990538 cites W2169022369 @default.
- W2599990538 cites W2172201406 @default.
- W2599990538 cites W2173417946 @default.
- W2599990538 cites W2288675656 @default.
- W2599990538 cites W2309413820 @default.
- W2599990538 cites W2327641916 @default.
- W2599990538 cites W2329316201 @default.
- W2599990538 cites W2334668612 @default.
- W2599990538 cites W2520336676 @default.
- W2599990538 cites W4230405800 @default.
- W2599990538 doi "https://doi.org/10.1016/j.neuropharm.2017.03.026" @default.
- W2599990538 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28347837" @default.
- W2599990538 hasPublicationYear "2017" @default.
- W2599990538 type Work @default.
- W2599990538 sameAs 2599990538 @default.
- W2599990538 citedByCount "19" @default.
- W2599990538 countsByYear W25999905382018 @default.
- W2599990538 countsByYear W25999905382019 @default.
- W2599990538 countsByYear W25999905382020 @default.
- W2599990538 countsByYear W25999905382021 @default.
- W2599990538 countsByYear W25999905382022 @default.
- W2599990538 countsByYear W25999905382023 @default.
- W2599990538 crossrefType "journal-article" @default.
- W2599990538 hasAuthorship W2599990538A5018631520 @default.
- W2599990538 hasAuthorship W2599990538A5036088530 @default.
- W2599990538 hasAuthorship W2599990538A5048987262 @default.
- W2599990538 hasAuthorship W2599990538A5052827662 @default.
- W2599990538 hasAuthorship W2599990538A5059539564 @default.
- W2599990538 hasAuthorship W2599990538A5060061391 @default.
- W2599990538 hasAuthorship W2599990538A5060488022 @default.
- W2599990538 hasAuthorship W2599990538A5061660173 @default.
- W2599990538 hasConcept C118303440 @default.
- W2599990538 hasConcept C126322002 @default.
- W2599990538 hasConcept C15490471 @default.
- W2599990538 hasConcept C163170386 @default.
- W2599990538 hasConcept C170493617 @default.
- W2599990538 hasConcept C185592680 @default.
- W2599990538 hasConcept C2776468701 @default.
- W2599990538 hasConcept C2777107010 @default.
- W2599990538 hasConcept C2779245659 @default.
- W2599990538 hasConcept C2780820201 @default.
- W2599990538 hasConcept C2781063702 @default.
- W2599990538 hasConcept C42219234 @default.
- W2599990538 hasConcept C71924100 @default.
- W2599990538 hasConcept C98274493 @default.