Behaviorally-Mediated Entrainment of Whole-Body Metabolic Processes: Conservation and Evolutionary Development of Mitochondrial Respiratory Complexes
Jazyk angličtina Země Spojené státy americké Médium electronic
Typ dokumentu úvodníky
PubMed
31809494
PubMed Central
PMC6911308
DOI
10.12659/msm.920174
PII: 920174
Knihovny.cz E-zdroje
- MeSH
- adenosintrifosfát metabolismus MeSH
- buněčné dýchání fyziologie MeSH
- energetický metabolismus MeSH
- lidé MeSH
- mitochondrie metabolismus fyziologie MeSH
- oxid dusnatý metabolismus MeSH
- relaxace fyziologie MeSH
- spotřeba kyslíku fyziologie MeSH
- teoretické modely MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- úvodníky MeSH
- Názvy látek
- adenosintrifosfát MeSH
- oxid dusnatý MeSH
The relaxation response derives its health benefits by reestablishing "normal" equilibria between the sympathetic and parasympathetic branches of the autonomic nervous system. Recent work suggests that this behavioral training provides positive effects on mitochondrial bioenergetics, insulin secretion, and reductions in pro-inflammatory and stress-related pathways. We have previously contended, however, that correlative associations of relaxation training with positive changes in gene expression in selected biological systems are strongly suggestive of adaptive physiological changes, but do not elucidate an underlying, clinically compelling, unified mechanism of action consistent with its purported positive health effects. We surmise that any plausible model of behaviorally-mediated regulatory effects on whole-body metabolic processes must be intrinsically broad-based and multifaceted via integration of differential contributions of functionally interactive peripheral and CNS organ systems. Accordingly, the initiation of multiple cellular protective/anti-bio-senescence processes may have emerged during evolutionary development to ensure the survival of hybrid prokaryotic/eukaryotic progenitor cells, given the evolvement of oxidative metabolism and its associated negative byproducts. As an essential corollary, preservation and adaptation of multifaceted regulatory molecules, notably nitric oxide, paralleled the development of eukaryotic cell types via multifaceted stereo-selective recognition and conformational matching by complex biochemical and molecular enzyme systems. Hence, the relaxation response may be a manifestation of a metabolic corrective process/response, that may now include cognition ("awareness").
Zobrazit více v PubMed
Beary JF, Benson H. A simple psychophysiological technique which elicits the hypometabolic changes of the relaxation respone. Psychosom Med. 1974;36(2):115–20. PubMed
Benson H. The relaxation response. New York: William Morrow; 1975.
Bhasin MK, Dusek JA, Chang BH, et al. Relaxation response induces temporal transcriptome changes in energy metabolism, insulin secretion and inflammatory pathways. PLoS One. 2013;8(5):e62817. PubMed PMC
Stefano GB, Esch T, Kream RM. Augmentation of whole-body metabolic status by mind-body training: Synchronous integration of tissue- and organ-specific mitochondrial function. Med Sci Monit Basic Res. 2019;25:8–14. PubMed PMC
Wei GX, Si G, Tang YY. Editorial: Brain-mind-body practice and health. Front Psychol. 2017;8:1886. PubMed PMC
Bates TE, Loesch A, Burnstock G, Clark JB. Mitochondrial nitric oxide synthase: A ubiquitous regulator of oxidative phosphorylation? Biochem Biophys Res Commun. 1996;218(1):40–44. PubMed
Stefano GB, Kream RM. Nitric oxide regulation of mitochondrial processes: Commonality in medical disorders. Ann Transplant. 2015;20:402–7. PubMed
Kream RM, Stefano GB. Endogenous morphine and nitric oxide coupled regulation of mitochondrial processes. Med SciMonit. 2009;15(12):RA263–68. PubMed
Stefano GB, Kream RM. Reciprocal regulation of cellular nitric oxide formation by nitric oxide synthase and nitrite reductases. Med Sci Monit. 2011;17(10):RA221–26. PubMed PMC
Stefano GB, Kream RM. Dysregulated mitochondrial and chloroplast bioenergetics from a translational medical perspective (review) Int J Mol Med. 2016;37:547–55. PubMed PMC
Shen W, Xu X, Ochoa M, et al. Role of nitric oxide in the regulation of oxygen consumption in conscious dogs. Circ Res. 1994;75(6):1086–95. PubMed
Brown GC. Nitric oxide and mitochondrial respiration. Biochim Biophys Acta. 1999;1411(2–3):351–69. PubMed
Schweizer M, Richter C. Nitric oxide potently and reversibly deenergizes mitochondria at low oxygen tension. Biochem Biophys Res Commun. 1994;204(1):169–75. PubMed
Takehara Y, Kanno T, Yoshioka T, et al. Oxygen-dependent regulation of mitochondrial energy metabolism by nitric oxide. Arch Biochem Biophys. 1995;323(1):27–32. PubMed
Giulivi C, Kato K, Cooper CE. Nitric oxide regulation of mitochondrial oxygen consumption I: Cellular physiology. Am J Physiol Cell Physiol. 2006;291(6):C1225–31. PubMed
Shiva S. Mitochondria as metabolizers and targets of nitrite. Nitric Oxide. 2010;22(2):64–74. PubMed PMC
Shiva S, Brookes PS, Patel RP, et al. Nitric oxide partitioning into mitochondrial membranes and the control of respiration at cytochrome c oxidase. Proc Natl Acad Sci USA. 2001;98(13):7212–17. PubMed PMC
Stefano GB, Mantione KJ, Casares FM, Kream RM. Anaerobically functioning mitochondria: Evolutionary perspective on modulation of energy metabolism in Mytilus edulis. Invertebrate Survival Journal. 2015;12:22–28.
Stefano GB, Kream RM. Hypoxia defined as a common culprit/initiation factor in mitochondrial-mediated proinflammatory processes. Med Sci Monit. 2015;21:1478–84. PubMed PMC
Shiva S. Nitrite: A physiological store of nitric oxide and modulator of mitochondrial function. Redox Biol. 2013;1(1):40–44. PubMed PMC
Stefano GB. Conformational matching: a possible evolutionary force in the evolvement of signal systems. In: Stefano GB, editor. CRC Handbook of comparative opioid and related neuropeptide mechanisms. Boca Raton: CRC Press Inc; 1986. pp. 271–77.
Stefano GB, Pilonis N, Ptacek R, et al. Gut, microbiome, and brain regulatory axis: Relevance to neurodegenerative and psychiatric disorders. Cell Mol Neurobiol. 2018;38:1197–206. PubMed PMC
Esch T, Kream RM, Stefano GB. Chromosomal processes in mind-body medicine: Chronic stress, cell aging, and telomere length. Med Sci Monit Bas Res. 2018;24:134–40. PubMed PMC