The effects of peripherally-subacute treatment with irisin on hippocampal dendritogenesis and astrocyte-secreted factors

Fibronectin type III domain containing 5 (FNDC5)/irisin is an exercise-induced myokine, which contributes to cognitive functions. However, the relationship between the neuroprotective effects of FNDC5/irisin and hippocampal dendritic remodeling and astrocyte-secreted factors remains unclear. Therefo...

Full description

Saved in:
Bibliographic Details
Published inJournal of exercise nutrition & biochemistry Vol. 23; no. 4; pp. 32 - 35
Main Authors Kim, Mun-Hee, Leem, Yea-Hyun
Format Journal Article
LanguageEnglish
Published Korea (South) 한국운동영양학회 31.12.2019
Subjects
Online AccessGet full text
ISSN2233-6842
2233-6834
2233-6842
DOI10.20463/jenb.2019.0029

Cover

Loading…
More Information
Summary:Fibronectin type III domain containing 5 (FNDC5)/irisin is an exercise-induced myokine, which contributes to cognitive functions. However, the relationship between the neuroprotective effects of FNDC5/irisin and hippocampal dendritic remodeling and astrocyte-secreted factors remains unclear. Therefore, we explored whether subchronic recombinant irisin treatment affected hippocampal morphology and some astrocyte-derived molecules. Mice were intraperitoneally injected with irisin (0.5 μg/kg/day) for seven days, followed by their sacrifice two days later. Hippocampal morphometric parameters were analyzed and pgc-1a, fndc5, bdnf, and some astrocyte-derived factors mRNA levels were measured. Dendritic length, arborization, and spine density were enhanced by irisin regimen in hippocampal CA1 and CA3 areas. Hippocampal pgc-1a, fndc5, and bdnf mRNA levels were significantly increased by irisin treatment. Moreover, hevin mRNA levels were significantly enhanced, whereas tgf-b1 levels downregulated by irisin treatment. FNDC5/irisin has dendritogenic activity probably through hevin induction and TGF-β1 suppression.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2233-6842
2233-6834
2233-6842
DOI:10.20463/jenb.2019.0029