SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Nyberg Erik 1986 )
 

Sökning: WFRF:(Nyberg Erik 1986 ) > Toxic Impact of Ana...

Toxic Impact of Anabolic Androgenic Steroids in Primary Rat Cortical Cell Cultures

Zelleroth, Sofia, 1990- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Biologisk beroendeforskning
Nylander, Erik, 1986- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Biologisk beroendeforskning
Nyberg, Fred, 1945- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Biologisk beroendeforskning
visa fler...
Grönbladh, Alfhild, 1983- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Biologisk beroendeforskning
Hallberg, Mathias, 1971- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Biologisk beroendeforskning
visa färre...
 (creator_code:org_t)
Elsevier BV, 2019
2019
Engelska.
Ingår i: Neuroscience. - : Elsevier BV. - 0306-4522 .- 1873-7544. ; 397, s. 172-183
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The use of anabolic androgenic steroids (AASs) among non-athletes is a public health-problem, as abusers underestimate the negative effects associated with these drugs. The present study investigated the toxic effects of testosterone, nandrolone, stanozolol, and trenbolone, and aimed to understand how AAS abuse affects the brain. Mixed cortical cultures from embryonic rats were grown in vitro for 7 days and thereafter treated with increasing concentrations of AASs for 24 h (single-dose) or 3 days (repeated exposure). Cells were co-treated with the androgen-receptor (AR) antagonist flutamide, to determine whether the potential adverse effects observed were mediated by the AR. Cellular toxicity was determined by measuring mitochondrial activity, lactate dehydrogenase (LDH) release, and caspase-3/7 activity. Nandrolone, unlike the other AASs studied, indicated an effect on mitochondrial activity after 24 h. Furthermore, single-dose exposure with testosterone, nandrolone and trenbolone increased LDH release, while no effect was detected with stanozolol. However, all of the four steroids negatively affected mitochondrial function and resulted in LDH release after repeated exposure. Testosterone, nandrolone, and trenbolone caused their toxic effects by induction of apoptosis, unlike stanozolol that seemed to induce necrosis. Flutamide almost completely prevented AAS-induced toxicity by maintaining mitochondrial function, cellular integrity, and inhibition of apoptosis. Overall, we found that supra-physiological concentrations of AASs induce cell death in mixed primary cortical cultures, but to different extents, and possibly through various mechanisms. The data presented herein suggest that the molecular interactions of the AASs with the AR are primarily responsible for the toxic outcomes observed.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Nyckelord

mitochondrial function membrane integrity cell death androgen-receptor flutamide
Farmaceutisk vetenskap
Pharmaceutical Science

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy