FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2016073125> ?p ?o ?g. }

• W2016073125 endingPage "207" @default.
• W2016073125 startingPage "202" @default.
• W2016073125 abstract "Sleep apnea (SA) causes not only sleep disturbances, but also neurocognitive impairments and/or psychoemotional disorders. Here, we studied the effects of intermittent hypoxia (IH) on forebrain Fos expression using obese diabetic db/db mice to explore the pathophysiological alterations in neural activities and the brain regions related to SA syndrome. Male db/db mice were exposed to IH stimuli (repetitive 6-min cycles of 1min with 5% oxygen followed by 5min with 21% oxygen) for 8h (80 cycles) per day or normoxic condition (control group) for 14 days. Fos protein expression was immunohistochemically examined a day after the last IH exposure. Mapping analysis revealed a significant reduction of Fos expression by IH in limbic and paralimbic structures, including the cingulate and piriform cortices, the core part of the nucleus accumbens and most parts of the amygdala (i.e., the basolateral and basomedial amygdaloid nuclei, cortical amygdaloid area and medial amygdaloid nucleus). In the brain stem regions, Fos expression was region-specifically reduced in the ventral tegmental area while other regions including the striatum, thalamus and hypothalamus, were relatively resistant against IH. In addition, db/db mice exposed to IH showed a trend of sedative and/or depressive behavioral signs in the open field and forced swim tests. The present results illustrate that SA in the obese diabetic model causes neural suppression preferentially in the limbic and paralimbic regions, which may be related to the neuropsychological disturbances associated with SA." @default.
• W2016073125 created "2016-06-24" @default.
• W2016073125 creator A5007422276 @default.
• W2016073125 creator A5010916565 @default.
• W2016073125 creator A5011049221 @default.
• W2016073125 creator A5013647008 @default.
• W2016073125 creator A5015371472 @default.
• W2016073125 creator A5030739148 @default.
• W2016073125 creator A5044708206 @default.
• W2016073125 creator A5045907284 @default.
• W2016073125 creator A5050238592 @default.
• W2016073125 creator A5067266977 @default.
• W2016073125 creator A5075433231 @default.
• W2016073125 creator A5078141659 @default.
• W2016073125 creator A5081585524 @default.
• W2016073125 creator A5084056727 @default.
• W2016073125 date "2013-12-01" @default.
• W2016073125 modified "2023-09-26" @default.
• W2016073125 title "Preferential suppression of limbic Fos expression by intermittent hypoxia in obese diabetic mice" @default.
• W2016073125 cites W1797972710 @default.
• W2016073125 cites W1962596608 @default.
• W2016073125 cites W1967473292 @default.
• W2016073125 cites W1969391575 @default.
• W2016073125 cites W1969394902 @default.
• W2016073125 cites W1970175928 @default.
• W2016073125 cites W1977957829 @default.
• W2016073125 cites W1988629142 @default.
• W2016073125 cites W1996692474 @default.
• W2016073125 cites W1998101177 @default.
• W2016073125 cites W1999624194 @default.
• W2016073125 cites W2010888510 @default.
• W2016073125 cites W2019546014 @default.
• W2016073125 cites W2025240330 @default.
• W2016073125 cites W2028025368 @default.
• W2016073125 cites W2028318252 @default.
• W2016073125 cites W2030284843 @default.
• W2016073125 cites W2034556696 @default.
• W2016073125 cites W2036241837 @default.
• W2016073125 cites W2041457323 @default.
• W2016073125 cites W2041545014 @default.
• W2016073125 cites W2045344970 @default.
• W2016073125 cites W2052108626 @default.
• W2016073125 cites W2066771173 @default.
• W2016073125 cites W2075027890 @default.
• W2016073125 cites W2079926893 @default.
• W2016073125 cites W2102740359 @default.
• W2016073125 cites W2111232488 @default.
• W2016073125 cites W2114168282 @default.
• W2016073125 cites W2115476973 @default.
• W2016073125 cites W2123072375 @default.
• W2016073125 cites W2148535867 @default.
• W2016073125 cites W2151803734 @default.
• W2016073125 cites W2155858211 @default.
• W2016073125 cites W2159317713 @default.
• W2016073125 cites W2168660234 @default.
• W2016073125 doi "https://doi.org/10.1016/j.neures.2013.09.013" @default.
• W2016073125 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24144732" @default.
• W2016073125 hasPublicationYear "2013" @default.
• W2016073125 type Work @default.
• W2016073125 sameAs 2016073125 @default.
• W2016073125 citedByCount "7" @default.
• W2016073125 countsByYear W20160731252016 @default.
• W2016073125 countsByYear W20160731252017 @default.
• W2016073125 countsByYear W20160731252020 @default.
• W2016073125 countsByYear W20160731252021 @default.
• W2016073125 crossrefType "journal-article" @default.
• W2016073125 hasAuthorship W2016073125A5007422276 @default.
• W2016073125 hasAuthorship W2016073125A5010916565 @default.
• W2016073125 hasAuthorship W2016073125A5011049221 @default.
• W2016073125 hasAuthorship W2016073125A5013647008 @default.
• W2016073125 hasAuthorship W2016073125A5015371472 @default.
• W2016073125 hasAuthorship W2016073125A5030739148 @default.
• W2016073125 hasAuthorship W2016073125A5044708206 @default.
• W2016073125 hasAuthorship W2016073125A5045907284 @default.
• W2016073125 hasAuthorship W2016073125A5050238592 @default.
• W2016073125 hasAuthorship W2016073125A5067266977 @default.
• W2016073125 hasAuthorship W2016073125A5075433231 @default.
• W2016073125 hasAuthorship W2016073125A5078141659 @default.
• W2016073125 hasAuthorship W2016073125A5081585524 @default.
• W2016073125 hasAuthorship W2016073125A5084056727 @default.
• W2016073125 hasConcept C126322002 @default.
• W2016073125 hasConcept C134018914 @default.
• W2016073125 hasConcept C137183658 @default.
• W2016073125 hasConcept C15744967 @default.
• W2016073125 hasConcept C169760540 @default.
• W2016073125 hasConcept C169900460 @default.
• W2016073125 hasConcept C2776006263 @default.
• W2016073125 hasConcept C2776552330 @default.
• W2016073125 hasConcept C2777003273 @default.
• W2016073125 hasConcept C2778402161 @default.
• W2016073125 hasConcept C2779144063 @default.
• W2016073125 hasConcept C2779246727 @default.
• W2016073125 hasConcept C2779715522 @default.
• W2016073125 hasConcept C2780451725 @default.
• W2016073125 hasConcept C2780796939 @default.
• W2016073125 hasConcept C2780948874 @default.
• W2016073125 hasConcept C2781210436 @default.
• W2016073125 hasConcept C513476851 @default.

• next