-
Je něco špatně v tomto záznamu ?
Altered sex differences related to food intake, hedonic preference, and FosB/deltaFosB expression within central neural circuit involved in homeostatic and hedonic food intake regulation in Shank3B mouse model of autism spectrum disorder
Z. Pirník, I. Szadvári, V. Borbélyová, A. Tomova
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
- MeSH
- homeostáza * fyziologie MeSH
- mikrofilamentové proteiny * genetika metabolismus MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední C57BL MeSH
- myši knockoutované MeSH
- myši MeSH
- pohlavní dimorfismus * MeSH
- poruchy autistického spektra * genetika metabolismus MeSH
- preference v jídle fyziologie MeSH
- přijímání potravy * fyziologie genetika MeSH
- proteiny nervové tkáně * genetika MeSH
- protoonkogenní proteiny c-fos metabolismus biosyntéza MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Autism spectrum disorder (ASD) is a neurodevelopmental disorder accompanied by narrow interests, difficulties in communication and social interaction, and repetitive behavior. In addition, ASD is frequently associated with eating and feeding problems. Although the symptoms of ASD are more likely to be observed in boys, the prevalence of eating disorders is more common in females. The ingestive behavior is regulated by the integrative system of the brain, which involves both homeostatic and hedonic neural circuits. Sex differences in the physiology of food intake depend on sex hormones regulating the expression of the ASD-associated Shank genes. Shank3 mutation leads to ASD-like traits and Shank3B -/- mice have been established as an animal model to study the neurobiology of ASD. Therefore, the long-lasting neuronal activity in the central neural circuit related to the homeostatic and hedonic regulation of food intake was evaluated in both sexes of Shank3B mice, followed by the evaluation of the food intake and preference. In the Shank3B +/+ genotype, well-preserved relationships in the tonic activity within the homeostatic neural network together with the relationships between ingestion and hedonic preference were observed in males but were reduced in females. These interrelations were partially or completely lost in the mice with the Shank3B -/- genotype. A decreased hedonic preference for the sweet taste but increased total food intake was found in the Shank3B -/- mice. In the Shank3B -/- group, there were altered sex differences related to the amount of tonic cell activity in the hedonic and homeostatic neural networks, together with altered sex differences in sweet and sweet-fat solution intake. Furthermore, the Shank3B -/- females exhibited an increased intake and preference for cheese compared to the Shank3B +/+ ones. The obtained data indicate altered functional crosstalk between the central homeostatic and hedonic neural circuits involved in the regulation of food intake in ASD.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25003191
- 003
- CZ-PrNML
- 005
- 20250206104109.0
- 007
- ta
- 008
- 250121e20241024enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.neuint.2024.105895 $2 doi
- 035 __
- $a (PubMed)39461669
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Pirník, Zdenko $u Institute of Physiology, Faculty of Medicine, Comenius University in Bratislava, Bratislava, Slovakia; Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of Sciences, Bratislava, Slovakia; Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Prague, Czech Republic. Electronic address: zdenko.pirnik@fmed.uniba.sk
- 245 10
- $a Altered sex differences related to food intake, hedonic preference, and FosB/deltaFosB expression within central neural circuit involved in homeostatic and hedonic food intake regulation in Shank3B mouse model of autism spectrum disorder / $c Z. Pirník, I. Szadvári, V. Borbélyová, A. Tomova
- 520 9_
- $a Autism spectrum disorder (ASD) is a neurodevelopmental disorder accompanied by narrow interests, difficulties in communication and social interaction, and repetitive behavior. In addition, ASD is frequently associated with eating and feeding problems. Although the symptoms of ASD are more likely to be observed in boys, the prevalence of eating disorders is more common in females. The ingestive behavior is regulated by the integrative system of the brain, which involves both homeostatic and hedonic neural circuits. Sex differences in the physiology of food intake depend on sex hormones regulating the expression of the ASD-associated Shank genes. Shank3 mutation leads to ASD-like traits and Shank3B -/- mice have been established as an animal model to study the neurobiology of ASD. Therefore, the long-lasting neuronal activity in the central neural circuit related to the homeostatic and hedonic regulation of food intake was evaluated in both sexes of Shank3B mice, followed by the evaluation of the food intake and preference. In the Shank3B +/+ genotype, well-preserved relationships in the tonic activity within the homeostatic neural network together with the relationships between ingestion and hedonic preference were observed in males but were reduced in females. These interrelations were partially or completely lost in the mice with the Shank3B -/- genotype. A decreased hedonic preference for the sweet taste but increased total food intake was found in the Shank3B -/- mice. In the Shank3B -/- group, there were altered sex differences related to the amount of tonic cell activity in the hedonic and homeostatic neural networks, together with altered sex differences in sweet and sweet-fat solution intake. Furthermore, the Shank3B -/- females exhibited an increased intake and preference for cheese compared to the Shank3B +/+ ones. The obtained data indicate altered functional crosstalk between the central homeostatic and hedonic neural circuits involved in the regulation of food intake in ASD.
- 650 _2
- $a zvířata $7 D000818
- 650 12
- $a poruchy autistického spektra $x genetika $x metabolismus $7 D000067877
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 12
- $a proteiny nervové tkáně $x genetika $7 D009419
- 650 12
- $a pohlavní dimorfismus $7 D012727
- 650 12
- $a mikrofilamentové proteiny $x genetika $x metabolismus $7 D008840
- 650 12
- $a homeostáza $x fyziologie $7 D006706
- 650 _2
- $a myši $7 D051379
- 650 12
- $a přijímání potravy $x fyziologie $x genetika $7 D004435
- 650 _2
- $a modely nemocí na zvířatech $7 D004195
- 650 _2
- $a preference v jídle $x fyziologie $7 D005518
- 650 _2
- $a myši inbrední C57BL $7 D008810
- 650 _2
- $a myši knockoutované $7 D018345
- 650 _2
- $a protoonkogenní proteiny c-fos $x metabolismus $x biosyntéza $7 D016760
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Szadvári, Ivan $u Institute of Physiology, Faculty of Medicine, Comenius University in Bratislava, Bratislava, Slovakia
- 700 1_
- $a Borbélyová, Veronika $u Institute of Molecular Biomedicine, Faculty of Medicine, Comenius University in Bratislava, Bratislava, Slovakia
- 700 1_
- $a Tomova, Aleksandra $u Institute of Physiology, Faculty of Medicine, Comenius University in Bratislava, Bratislava, Slovakia
- 773 0_
- $w MED00003485 $t Neurochemistry international $x 1872-9754 $g Roč. 181 (20241024), s. 105895
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39461669 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250121 $b ABA008
- 991 __
- $a 20250206104105 $b ABA008
- 999 __
- $a ok $b bmc $g 2263126 $s 1239198
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 181 $c - $d 105895 $e 20241024 $i 1872-9754 $m Neurochemistry international $n Neurochem Int $x MED00003485
- LZP __
- $a Pubmed-20250121