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Lipopolysaccharide-induced changes in the kynurenine pathway and symptoms of sickness behavior in humans

Balter, Leonie J. T. (författare)
Stockholms universitet,Stressforskningsinstitutet,Biologisk psykologi,Karolinska Institutet, Sweden
Li, Xueqi (författare)
Schwieler, Lilly (författare)
Karolinska Institutet
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Erhardt, Sophie (författare)
Axelsson, John (författare)
Stockholms universitet,Stressforskningsinstitutet,Biologisk psykologi,Karolinska Institutet, Sweden
Olsson, Mats J. (författare)
Karolinska Institutet
Lasselin, Julie (författare)
Stockholms universitet,Stressforskningsinstitutet,Biologisk psykologi,Karolinska Institutet, Sweden
Lekander, Mats, 1959- (författare)
Stockholms universitet,Stressforskningsinstitutet,Biologisk psykologi,Karolinska Institutet, Sweden
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 (creator_code:org_t)
2023
2023
Engelska.
Ingår i: Psychoneuroendocrinology. - 0306-4530 .- 1873-3360. ; 153
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Metabolites of the kynurenine pathway are hypothesized to be implicated in inflammation-associated depression, but there is a lack of experimental studies in humans assessing the kinetics of kynurenine metabolites in relation to experimentally-induced sickness. The aim of the present study was to assess changes in the kynurenine pathway and to explore its relation to symptoms of sickness behavior during an acute experimental immune challenge.This double-blind placebo-controlled randomized cross-over study included 22 healthy human participants (n = 21 both sessions, Mage = 23.4, SD = 3.6, nine women) who received an intravenous injection of 2.0 ng/kg lipopolysaccharide (LPS) and saline (placebo) on two different occasions in a randomized order. Blood samples (0 h, 1 h, 1.5 h, 2 h, 3 h, 4 h, 5 h, 7 h post-injection) were analyzed for kynurenine metabolites and inflammatory cytokines. The intensity of symptoms of sickness behavior was assessed using the 10-item Sickness Questionnaire at 0 h, 1.5 h, 3 h, 5 h, and 7 h post-injection.LPS induced significantly lower concentrations of plasma tryptophan (at 2 h, 4 h, 5 h, and 7 h post-injection), kynurenine (at 2 h, 3 h, 4 h, and 5 h post-injection), nicotinamide (at 4 h, 5 h, and 7 h post-injection), and higher levels for quinolinic acid at 5 h post-injection as compared to placebo. LPS did not affect kynurenic acid, 3-hydroxykynurenine, and picolinic acid. The development of the sickness symptoms was largely similar across items, with the highest levels around 1.5–3 h post-injection. Changes in plasma levels of kynurenine metabolites seem to coincide rather than precede or follow changes in subjective sickness. Exploratory analyses indicate that higher Sickness Questionnaire total scores at 1.5–5 h post-injection were correlated with lower kynurenic acid and nicotinamide levels.These results lend further support for LPS-induced changes in the kynurenine pathway, but may not, as interpreted from blood levels, causally link to LPS-induced acute symptoms of sickness behavior. Future research may consider a larger sample to further scrutinize the role of the kynurenine pathway in the sickness response.

Ämnesord

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

Nyckelord

kynurenine pathway
lipopolysaccharides
sickness behavior
depression
tryptophan
psykologi
Psychology

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