Relaxation response induces temporal transcriptome changes in energy metabolism, insulin secretion and inflammatory pathways
PloS one
Short Title:
PLoS One
Format:
Journal Article
Publication Date:
Nov 30, 2012
Pages:
e62817
Sources ID:
70121
Notes:
LR: 20170221; GR: H75/CCH123424/PHS HHS/United States; GR: M01 RR01032/RR/NCRR NIH HHS/United States; GR: R01 AT006464-01/AT/NCCIH NIH HHS/United States; GR: R01 DP000339/DP/NCCDPHP CDC HHS/United States; JID: 101285081; 0 (Inflammation Mediators); 0 (Insulin); 31C4KY9ESH (Nitric Oxide); EIN: PLoS One. 2017 Feb 21;12 (2):e0172873. PMID: 28222196; 2012/10/09 00:00 [received]; 2013/03/26 00:00 [accepted]; 2013/05/08 06:00 [entrez]; 2013/05/08 06:00 [pubmed]; 2013/12/16 06:00 [medline]; epublish
Collection:
Yoga-Based Interventions for Stress and Anxiety
Visibility:
Public (group default)
Abstract:
(Show)
The relaxation response (RR) is the counterpart of the stress response. Millennia-old practices evoking the RR include meditation, yoga and repetitive prayer. Although RR elicitation is an effective therapeutic intervention that counteracts the adverse clinical effects of stress in disorders including hypertension, anxiety, insomnia and aging, the underlying molecular mechanisms that explain these clinical benefits remain undetermined. To assess rapid time-dependent (temporal) genomic changes during one session of RR practice among healthy practitioners with years of RR practice and also in novices before and after 8 weeks of RR training, we measured the transcriptome in peripheral blood prior to, immediately after, and 15 minutes after listening to an RR-eliciting or a health education CD. Both short-term and long-term practitioners evoked significant temporal gene expression changes with greater significance in the latter as compared to novices. RR practice enhanced expression of genes associated with energy metabolism, mitochondrial function, insulin secretion and telomere maintenance, and reduced expression of genes linked to inflammatory response and stress-related pathways. Interactive network analyses of RR-affected pathways identified mitochondrial ATP synthase and insulin (INS) as top upregulated critical molecules (focus hubs) and NF-kappaB pathway genes as top downregulated focus hubs. Our results for the first time indicate that RR elicitation, particularly after long-term practice, may evoke its downstream health benefits by improving mitochondrial energy production and utilization and thus promoting mitochondrial resiliency through upregulation of ATPase and insulin function. Mitochondrial resiliency might also be promoted by RR-induced downregulation of NF-kappaB-associated upstream and downstream targets that mitigates stress.