Behavioral conditioning of anti-proliferative and immunosuppressive properties of the mTOR inhibitor rapamycin.
Animals
Avoidance Learning
/ physiology
CD4-Positive T-Lymphocytes
/ immunology
CD8-Positive T-Lymphocytes
/ immunology
Conditioning, Classical
/ drug effects
Cyclophosphamide
/ pharmacology
Cyclosporine
/ pharmacology
Immune Tolerance
/ drug effects
Immunosuppression Therapy
Immunosuppressive Agents
/ pharmacology
Interleukin-10
/ immunology
Male
Rats
Rats, Inbred F344
Rats, Inbred Strains
Saccharin
Sirolimus
/ metabolism
TOR Serine-Threonine Kinases
/ immunology
Taste
/ physiology
Anti-proliferative effects
Conditioned taste avoidance
Immunosuppression
Interleukin-10
Rapamycin
mTOR
Journal
Brain, behavior, and immunity
ISSN: 1090-2139
Titre abrégé: Brain Behav Immun
Pays: Netherlands
ID NLM: 8800478
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
received:
25
11
2018
revised:
05
02
2019
accepted:
02
04
2019
pubmed:
7
4
2019
medline:
14
5
2020
entrez:
7
4
2019
Statut:
ppublish
Résumé
Suppression of immune functions can be elicited by behavioral conditioning using drugs such as cyclosporine A, cyclophosphamide, or opioids. Nevertheless, little is known regarding the conditioned actions of clinically approved immunosuppressive drugs with distinct cell signaling pathways. The present study tested the assumption to condition immunopharmacological properties of rapamycin (sirolimus), a small-molecule drug widely used as anti-tumor medication and to prevent graft rejection. For this purpose, a conditioned taste avoidance (CTA) paradigm was used, pairing the presentation of a novel taste (saccharin) as conditioned stimulus (CS) with injections of rapamycin as unconditioned stimulus (US). Subsequent re-exposure to the CS at a later time revealed that conditioning with rapamycin induced an only moderate CTA. However, pronounced conditioned immunopharmacological effects were observed, reflected by significantly reduced levels of IL-10 cytokine production and diminished proliferation of splenic CD4
Identifiants
pubmed: 30953772
pii: S0889-1591(18)31159-0
doi: 10.1016/j.bbi.2019.04.013
pii:
doi:
Substances chimiques
Immunosuppressive Agents
0
Interleukin-10
130068-27-8
Cyclosporine
83HN0GTJ6D
Cyclophosphamide
8N3DW7272P
mTOR protein, rat
EC 2.7.1.1
TOR Serine-Threonine Kinases
EC 2.7.11.1
Saccharin
FST467XS7D
Sirolimus
W36ZG6FT64
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
326-331Informations de copyright
Copyright © 2019. Published by Elsevier Inc.