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Activation of PPAR gamma Attenuates the Expression of Physical and Affective Nicotine Withdrawal Symptoms through Mechanisms Involving Amygdala and Hippocampus Neurotransmission

Domi, Esi (författare)
Linköpings universitet,Centrum för social och affektiv neurovetenskap,Medicinska fakulteten,Univ Camerino, Italy
Caputi, Francesca Felicia (författare)
Alma Mater Studiorum Univ Bologna, Italy
Romualdi, Patrizia (författare)
Alma Mater Studiorum Univ Bologna, Italy
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Domi, Ana (författare)
Univ Camerino, Italy
Scuppa, Giulia (författare)
Univ Camerino, Italy
Candeletti, Sanzio (författare)
Alma Mater Studiorum Univ Bologna, Italy
Atkins, Alison Lynn (författare)
Linköpings universitet,Avdelning för neurobiologi,Medicinska fakulteten
Heilig, Markus (författare)
Linköpings universitet,Centrum för social och affektiv neurovetenskap,Medicinska fakulteten,Region Östergötland, Psykiatriska kliniken inkl beroendekliniken
Demopulos, Gregory (författare)
Omeros Corp, WA 98101 USA
Gaitanaris, George (författare)
Omeros Corp, WA 98101 USA
Ciccocioppo, Roberto (författare)
Univ Camerino, Italy
Ubaldi, Massimo (författare)
Univ Camerino, Italy
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 (creator_code:org_t)
SOC NEUROSCIENCE, 2019
2019
Engelska.
Ingår i: Journal of Neuroscience. - : SOC NEUROSCIENCE. - 0270-6474 .- 1529-2401. ; 39:49, s. 9864-9875
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • An isoform of peroxisome proliferator-activated receptors (PPARs), PPAR gamma, is the receptor for the thiazolidinedione class of antidiabetic medications including pioglitazone. Neuroanatomical data indicate PPAR gamma localization in brain areas involved in drug addiction. Preclinical and clinical data have shown that pioglitazone reduces alcohol and opioid self-administration, relapse to drug seeking, and plays a role in emotional responses. Here, we investigated the behavioral effect of PPAR gamma manipulation on nicotine withdrawal in male Wistar rats and in male mice with neuron-specific PPAR gamma deletion (PPAR gamma(()(+/+)())) and their littermate wild-type (PPAR gamma((-/-))) controls. Real-time quantitative RT-PCR and RNAscope in situ hybridization assays were used for assessing the levels of expression and cell-type localization of PPAR gamma function, Memory, Mortality, Older subjects, Structural brain abnormalities during nicotine withdrawal. Brain site-specific microinjections of the PPAR gamma agonist pioglitazone were performed to explore the role of this system on nicotine withdrawal at a neurocircuitry level. Results showed that activation of PPAR gamma by pioglitazone abolished the expression of somatic and affective nicotine withdrawal signs in rats and in (PPAR gamma(()(+/+)())) mice. This effect was blocked by the PPAR gamma antagonist GW9662. During early withdrawal and protracted abstinence, the expression of PPAR gamma increased in GABAergic and glutamatergic cells of the amygdala and hippocampus, respectively. Hippocampal microinjections of pioglitazone reduced the expression of the physical signs of withdrawal, whereas excessive anxiety associated with protracted abstinence was prevented by pioglitazone microinjection into the amygdala. Our results demonstrate the implication of the neuronal PPAR gamma in nicotine withdrawal and indicates that activation of PPAR gamma may offer an interesting strategy for smoking cessation.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Nyckelord

addiction; nicotine; pioglitazone; PPAR gamma; withdrawal

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