The role of nitric oxide signaling in food intake; insights from the inner mitochondrial membrane peptidase 2 mutant mice

Autor: Baisong Lu, Qingguo Zhao, Changjie Han
Jazyk: angličtina
Rok vydání: 2013
Předmět:
Male
Clinical Biochemistry
Mutant
Adipose tissue
Biochemistry
Eating
Mice
chemistry.chemical_compound
0302 clinical medicine
Food intake
NOS
nitric oxide synthase

Inner mitochondrial membrane
Cyclic GMP
lcsh:QH301-705.5
Cells
Cultured

Immp2l
IMP2 inner mitochondrial membrane peptidase-like

chemistry.chemical_classification
Regulation of gene expression
0303 health sciences
lcsh:R5-920
Superoxide
Brain
UCP2
uncoupling protein 2

Adipose Tissue
Female
Signal transduction
lcsh:Medicine (General)
Signal Transduction
Research Paper
medicine.medical_specialty
CART
cocaine- and amphetamine-regulated transcript

NPY
neuropeptide Y

CYC1
cytochrome c1

POMC
pro-opiomelanocortin

Biology
Nitric oxide
Mitochondrial Proteins
03 medical and health sciences
ROS
reactive oxygen species

AMPK
AMP-activated protein kinase

Internal medicine
Endopeptidases
medicine
Animals
AgRP
agouti related protein

GPD2
mitochondrial glycerol phosphate dehydrogenase

030304 developmental biology
Mutant mice
NO
nitric oxide

Reactive oxygen species
Body Weight
Organic Chemistry
ADSC
adipose-derived stromal cells

Endocrinology
Gene Expression Regulation
chemistry
lcsh:Biology (General)
Mutation
Immp2l
cGMP
cyclic guanosine monophosphate

Energy expenditure
Reactive Oxygen Species
030217 neurology & neurosurgery
Zdroj: Redox Biology, Vol 1, Iss 1, Pp 498-507 (2013)
Redox Biology
ISSN: 2213-2317
Popis: Reactive oxygen species have been implicated in feeding control through involvement in brain lipid sensing, and regulating NPY/AgRP and pro-opiomelanocortin (POMC) neurons, although the underlying mechanisms are unclear. Nitric oxide is a signaling molecule in neurons and it stimulates feeding in many species. Whether reactive oxygen species affect feeding through interaction with nitric oxide is unclear. We previously reported that Immp2l mutation in mice causes excessive mitochondrial superoxide generation, which causes infertility and early signs of aging. In our present study, reduced food intake in mutant mice resulted in significantly reduced body weight and fat composition while energy expenditure remained unchanged. Lysate from mutant brain showed a significant decrease in cGMP levels, suggesting insufficient nitric oxide signaling. Thus, our data suggests that reactive oxygen species may regulate food intake through modulating the bioavailability of nitric oxide.
Graphical abstract
Highlights • Mature adult Immp2l mutant mice have reduced body weight and fat composition. • Reduced body weight and fat composition is caused by reduced food intake. • Energy expenditure is not affected in mutant mice. • Brain cGMP level is lower in mutant mice.
Databáze: OpenAIRE