Guggulsterone Mediated JAK/STAT and PPAR-Gamma Modulation Prevents Neurobehavioral and Neurochemical Abnormalities in Propionic Acid-Induced Experimental Model of Autism.
Animals
Autism Spectrum Disorder
/ chemically induced
Disease Models, Animal
Female
Janus Kinases
/ metabolism
Male
Neuroprotective Agents
/ therapeutic use
PPAR gamma
/ metabolism
Pregnenediones
/ therapeutic use
Propionates
Rats, Wistar
STAT Transcription Factors
/ metabolism
Signal Transduction
/ drug effects
JAK/STAT
PPAR-gamma
autism
guggulsterone
neuroprotection
propionic acid
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
28 Jan 2022
28 Jan 2022
Historique:
received:
06
01
2022
revised:
21
01
2022
accepted:
27
01
2022
entrez:
15
2
2022
pubmed:
16
2
2022
medline:
22
2
2022
Statut:
epublish
Résumé
Autism spectrum disorder is a neurodevelopmental disorder marked by repetitive behaviour, challenges in verbal and non-verbal communication, poor socio-emotional health, and cognitive impairment. An increased level of signal transducer and activator of transcription 3 (STAT3) and a decreased level of peroxisome proliferator-activated receptor (PPAR) gamma have been linked to autism pathogenesis. Guggulsterone (GST) has a neuroprotective effect on autistic conditions by modulating these signalling pathways. Consequently, the primary objective of this study was to examine potential neuroprotective properties of GST by modulating JAK/STAT and PPAR-gamma levels in intracerebroventricular propionic acid (ICV PPA) induced experimental model of autism in adult rats. In this study, the first 11 days of ICV-PPA injections in rats resulted in autism-like behavioural, neurochemical, morphological, and histopathological changes. The above modifications were also observed in various biological samples, including brain homogenate, CSF, and blood plasma. GST was also observed to improve autism-like behavioural impairments in autistic rats treated with PPA, including locomotion, neuromuscular coordination, depression-like behaviour, spatial memory, cognition, and body weight. Prolonged GST treatment also restored neurochemical deficits in a dose-dependent manner. Chronic PPA administration increased STAT3 and decreased PPAR gamma in autistic rat brain, CSF, and blood plasma samples, which were reversed by GST. GST also restored the gross and histopathological alterations in PPA-treated rat brains. Our results indicate the neuroprotective effects of GST in preventing autism-related behavioural and neurochemical alterations.
Identifiants
pubmed: 35164154
pii: molecules27030889
doi: 10.3390/molecules27030889
pmc: PMC8839522
pii:
doi:
Substances chimiques
Neuroprotective Agents
0
PPAR gamma
0
Pregnenediones
0
Propionates
0
STAT Transcription Factors
0
pregna-4,17-diene-3,16-dione
A4PW148END
Janus Kinases
EC 2.7.10.2
propionic acid
JHU490RVYR
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Indo Soviet Friendship College of Pharmacy
ID : ISFCP/IAEC/CPCSEA/Meeting No: 27/2020/Protocol No.456
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