Matches in SemOpenAlex for { <https://semopenalex.org/work/W2014798765> ?p ?o ?g. }
- W2014798765 endingPage "49" @default.
- W2014798765 startingPage "43" @default.
- W2014798765 abstract "A major consequence of Parkinson's disease (PD) involves the loss of dopaminergic neurons in the substantia nigra (SN) and a subsequent loss of dopamine (DA) in the striatum. We have shown that glial cell line-derived neurotrophic factor (GDNF) shows robust restorative and protective effects for DA neurons in rats, non-human primates and possibly in humans. Despite GDNF's therapeutic potential, its clinical value has been questioned due to its limited diffusion to target areas from its large size and chemical structure. Several comparatively smaller peptides are thought to be generated from the prosequence. A five amino-acid peptide, dopamine neuron stimulating peptide-5 (DNSP-5), has been proposed to demonstrate biological activity relevant to neurodegenerative disease. We tested the in vitro effects of DNSP-5 in primary dopaminergic neurons dissected from the ventral mesencephalon of E14 Sprague Dawley rat fetuses. Cells were treated with several doses (0.03, 0.1, 1.0, 10.0 ng/mL) of GDNF, DNSP-5, or an equivalent volume of citrate buffer (vehicle). Morphological features of tyrosine hydroxylase positive neurons were quantified for each dose. DNSP-5 significantly increased (p < 0.001) all differentiation parameters compared to citrate vehicle (at one or more dose). For in vivo studies, a unilateral DNSP-5 treatment (30 μg) was administered directly to the SN. Microdialysis in the ipsilateral striatum was performed 28 days after treatment to determine extracellular levels of DA and its primary metabolites (3,4-dihydroxyphenylacetic acid and homovanillic acid). A single treatment significantly increased (~66%) extracellular DA levels compared to vehicle, while DA metabolites were unchanged. Finally, the protective effects of DNSP-5 against staurosporine-induced cytotoxicity were investigated in a neuronal cell line showing substantial protection by DNSP-5. Altogether, these studies strongly indicate biological activity of DNSP-5 and suggest that DNSP-5 has neurotrophic-like properties that may be relevant to the treatment of neurodegenerative diseases like PD." @default.
- W2014798765 created "2016-06-24" @default.
- W2014798765 creator A5013829647 @default.
- W2014798765 creator A5013951672 @default.
- W2014798765 creator A5016727567 @default.
- W2014798765 creator A5037708891 @default.
- W2014798765 creator A5040563604 @default.
- W2014798765 creator A5048761265 @default.
- W2014798765 creator A5050293094 @default.
- W2014798765 creator A5051602799 @default.
- W2014798765 creator A5059581239 @default.
- W2014798765 creator A5061363221 @default.
- W2014798765 date "2013-02-01" @default.
- W2014798765 modified "2023-10-17" @default.
- W2014798765 title "A synthetic five amino acid propeptide increases dopamine neuron differentiation and neurochemical function" @default.
- W2014798765 cites W102297612 @default.
- W2014798765 cites W1551575480 @default.
- W2014798765 cites W1583740060 @default.
- W2014798765 cites W1588182583 @default.
- W2014798765 cites W1795898662 @default.
- W2014798765 cites W1890054393 @default.
- W2014798765 cites W1900535849 @default.
- W2014798765 cites W1943060734 @default.
- W2014798765 cites W1969434975 @default.
- W2014798765 cites W1973178390 @default.
- W2014798765 cites W1974563583 @default.
- W2014798765 cites W1976749972 @default.
- W2014798765 cites W1983847788 @default.
- W2014798765 cites W1988463041 @default.
- W2014798765 cites W1989381407 @default.
- W2014798765 cites W1991208841 @default.
- W2014798765 cites W1996001296 @default.
- W2014798765 cites W1997631088 @default.
- W2014798765 cites W2005447847 @default.
- W2014798765 cites W2006747031 @default.
- W2014798765 cites W2019695510 @default.
- W2014798765 cites W2032554568 @default.
- W2014798765 cites W2034499699 @default.
- W2014798765 cites W2040137025 @default.
- W2014798765 cites W2051729090 @default.
- W2014798765 cites W2052450120 @default.
- W2014798765 cites W2053086497 @default.
- W2014798765 cites W2054810445 @default.
- W2014798765 cites W2057014510 @default.
- W2014798765 cites W2059383094 @default.
- W2014798765 cites W2065541320 @default.
- W2014798765 cites W2073986062 @default.
- W2014798765 cites W2079356832 @default.
- W2014798765 cites W2082559815 @default.
- W2014798765 cites W2086190854 @default.
- W2014798765 cites W2086802883 @default.
- W2014798765 cites W2103899142 @default.
- W2014798765 cites W2105696266 @default.
- W2014798765 cites W2145337544 @default.
- W2014798765 cites W2152718734 @default.
- W2014798765 cites W2153669485 @default.
- W2014798765 cites W2154452702 @default.
- W2014798765 cites W2163815564 @default.
- W2014798765 cites W2170077596 @default.
- W2014798765 cites W2203444202 @default.
- W2014798765 cites W2212123487 @default.
- W2014798765 cites W2471449461 @default.
- W2014798765 cites W83222092 @default.
- W2014798765 cites W2467292408 @default.
- W2014798765 doi "https://doi.org/10.1016/j.npep.2012.08.004" @default.
- W2014798765 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3558608" @default.
- W2014798765 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22981157" @default.
- W2014798765 hasPublicationYear "2013" @default.
- W2014798765 type Work @default.
- W2014798765 sameAs 2014798765 @default.
- W2014798765 citedByCount "3" @default.
- W2014798765 countsByYear W20147987652013 @default.
- W2014798765 countsByYear W20147987652016 @default.
- W2014798765 crossrefType "journal-article" @default.
- W2014798765 hasAuthorship W2014798765A5013829647 @default.
- W2014798765 hasAuthorship W2014798765A5013951672 @default.
- W2014798765 hasAuthorship W2014798765A5016727567 @default.
- W2014798765 hasAuthorship W2014798765A5037708891 @default.
- W2014798765 hasAuthorship W2014798765A5040563604 @default.
- W2014798765 hasAuthorship W2014798765A5048761265 @default.
- W2014798765 hasAuthorship W2014798765A5050293094 @default.
- W2014798765 hasAuthorship W2014798765A5051602799 @default.
- W2014798765 hasAuthorship W2014798765A5059581239 @default.
- W2014798765 hasAuthorship W2014798765A5061363221 @default.
- W2014798765 hasBestOaLocation W20147987652 @default.
- W2014798765 hasConcept C126322002 @default.
- W2014798765 hasConcept C134018914 @default.
- W2014798765 hasConcept C137183658 @default.
- W2014798765 hasConcept C159167319 @default.
- W2014798765 hasConcept C160539049 @default.
- W2014798765 hasConcept C169760540 @default.
- W2014798765 hasConcept C170493617 @default.
- W2014798765 hasConcept C185592680 @default.
- W2014798765 hasConcept C185856081 @default.
- W2014798765 hasConcept C25876315 @default.
- W2014798765 hasConcept C2775841634 @default.
- W2014798765 hasConcept C2775864247 @default.
- W2014798765 hasConcept C2775905480 @default.