Matches in SemOpenAlex for { <https://semopenalex.org/work/W2967718877> ?p ?o ?g. }
- W2967718877 endingPage "5040" @default.
- W2967718877 startingPage "5025" @default.
- W2967718877 abstract "We demonstrated optical activation of primary somatosensory afferents with high selectivity to fast-conducting fibres by means of adeno-associated virus 9 (AAV9)-mediated gene transduction in dorsal root ganglion (DRG) neurons. AVV9 expressing green fluorescent protein showed high selectivity and transduction efficiency for fast-conducting, large-sized DRG neurons. Compared with conventional electrical stimulation, optically elicited volleys in primary afferents had higher sensitivity with stimulus amplitude, but lower sensitivity with stimulus frequency. Optically elicited dorsal root volleys activated postsynaptic neurons in the segmental spinal pathway. This proposed technique will help establish the causal relationships between somatosensory afferent inputs and neural responses in the CNS as well as behavioural outcomes in higher mammals where transgenic animals are not available.Previously, fundamental structures and their mode of action in the spinal reflex circuit were determined by confirming their input-output relationship using electrophysiological techniques. In those experiments, the electrical stimulation of afferent fibres was used as a core element to identify different types of reflex pathways; however, a major disadvantage of this technique is its non-selectivity. In this study, we investigated the selective activation of large-diameter afferents by optogenetics combined with a virus vector transduction technique (injection via the sciatic nerve) in non-transgenic male Jcl:Wistar rats. We found that green fluorescent protein gene transduction of rat dorsal root ganglion (DRG) neurons with a preference for medium-to-large-sized cells was achieved using the adeno-associated virus 9 (AAV9) vector compared with the AAV6 vector (P = 0.021). Furthermore, the optical stimulation of Channelrhodopsin 2 (ChR2)-expressing DRG neurons (transduced by AAV9) produced compound action potentials in afferent nerves originating from fast-conducting nerve fibres. We also confirmed that physiological responses to different stimulus amplitudes were comparable between optogenetic and electrophysiological activation. However, compared with electrically elicited responses, the optically elicited responses had lower sensitivity with stimulus frequency. Finally, we showed that afferent volleys evoked by optical stimulation were sufficient to activate postsynaptic neurons in the spinal reflex arc. These results provide new ways for understanding the role of sensory afferent input to the central nervous system regarding behavioural control, especially when genetically manipulated animals are not available, such as higher mammals including non-human primates." @default.
- W2967718877 created "2019-08-22" @default.
- W2967718877 creator A5008078468 @default.
- W2967718877 creator A5025328770 @default.
- W2967718877 creator A5040667714 @default.
- W2967718877 creator A5059427033 @default.
- W2967718877 creator A5069224135 @default.
- W2967718877 creator A5070023754 @default.
- W2967718877 creator A5084824641 @default.
- W2967718877 date "2019-08-28" @default.
- W2967718877 modified "2023-10-15" @default.
- W2967718877 title "Optogenetic recruitment of spinal reflex pathways from large‐diameter primary afferents in non‐transgenic rats transduced with AAV9/Channelrhodopsin 2" @default.
- W2967718877 cites W1540607329 @default.
- W2967718877 cites W1747533618 @default.
- W2967718877 cites W1878468192 @default.
- W2967718877 cites W1965363502 @default.
- W2967718877 cites W1970839656 @default.
- W2967718877 cites W1975574255 @default.
- W2967718877 cites W1976627923 @default.
- W2967718877 cites W1978838450 @default.
- W2967718877 cites W1998085200 @default.
- W2967718877 cites W2004988025 @default.
- W2967718877 cites W2008289270 @default.
- W2967718877 cites W2015634109 @default.
- W2967718877 cites W2021493985 @default.
- W2967718877 cites W2024230789 @default.
- W2967718877 cites W2025645467 @default.
- W2967718877 cites W2026920679 @default.
- W2967718877 cites W2029105646 @default.
- W2967718877 cites W2033072655 @default.
- W2967718877 cites W2034503413 @default.
- W2967718877 cites W2035233735 @default.
- W2967718877 cites W2041229780 @default.
- W2967718877 cites W2042847772 @default.
- W2967718877 cites W2056902643 @default.
- W2967718877 cites W2063210874 @default.
- W2967718877 cites W2064838071 @default.
- W2967718877 cites W2073418960 @default.
- W2967718877 cites W2073572813 @default.
- W2967718877 cites W2073940113 @default.
- W2967718877 cites W2077821607 @default.
- W2967718877 cites W2081123138 @default.
- W2967718877 cites W2083932518 @default.
- W2967718877 cites W2092587499 @default.
- W2967718877 cites W2092757238 @default.
- W2967718877 cites W2099002565 @default.
- W2967718877 cites W2104579888 @default.
- W2967718877 cites W2109349667 @default.
- W2967718877 cites W2110095415 @default.
- W2967718877 cites W2110181951 @default.
- W2967718877 cites W2130121533 @default.
- W2967718877 cites W2139801134 @default.
- W2967718877 cites W2151917482 @default.
- W2967718877 cites W2167095271 @default.
- W2967718877 cites W2211603551 @default.
- W2967718877 cites W2346626276 @default.
- W2967718877 cites W2398054166 @default.
- W2967718877 cites W2418447373 @default.
- W2967718877 cites W2418592407 @default.
- W2967718877 cites W2473153144 @default.
- W2967718877 cites W2484015429 @default.
- W2967718877 cites W2490487642 @default.
- W2967718877 cites W2510758757 @default.
- W2967718877 cites W2564777270 @default.
- W2967718877 cites W2596596521 @default.
- W2967718877 cites W2766465734 @default.
- W2967718877 cites W2777690023 @default.
- W2967718877 cites W2780733918 @default.
- W2967718877 cites W2783656583 @default.
- W2967718877 cites W2799532100 @default.
- W2967718877 cites W2896045166 @default.
- W2967718877 cites W2905338839 @default.
- W2967718877 cites W2947351679 @default.
- W2967718877 cites W4210574564 @default.
- W2967718877 cites W4239908405 @default.
- W2967718877 doi "https://doi.org/10.1113/jp278292" @default.
- W2967718877 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6851594" @default.
- W2967718877 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31397900" @default.
- W2967718877 hasPublicationYear "2019" @default.
- W2967718877 type Work @default.
- W2967718877 sameAs 2967718877 @default.
- W2967718877 citedByCount "9" @default.
- W2967718877 countsByYear W29677188772020 @default.
- W2967718877 countsByYear W29677188772021 @default.
- W2967718877 countsByYear W29677188772022 @default.
- W2967718877 countsByYear W29677188772023 @default.
- W2967718877 crossrefType "journal-article" @default.
- W2967718877 hasAuthorship W2967718877A5008078468 @default.
- W2967718877 hasAuthorship W2967718877A5025328770 @default.
- W2967718877 hasAuthorship W2967718877A5040667714 @default.
- W2967718877 hasAuthorship W2967718877A5059427033 @default.
- W2967718877 hasAuthorship W2967718877A5069224135 @default.
- W2967718877 hasAuthorship W2967718877A5070023754 @default.
- W2967718877 hasAuthorship W2967718877A5084824641 @default.
- W2967718877 hasBestOaLocation W29677188771 @default.
- W2967718877 hasConcept C104317684 @default.
- W2967718877 hasConcept C105702510 @default.
- W2967718877 hasConcept C12554922 @default.