Relationship between human evolution and neurally mediated syncope disclosed by the polymorphic sites of the adrenergic receptor gene α2B-AR

• Published in: PloS one Vol. 10; no. 4; p. e0120788
• Main Authors: Komiyama, Tomoyoshi, Hirokawa, Takatsugu, Sato, Kyoko, Oka, Akira, Kamiguchi, Hiroshi, Nagata, Eiichiro, Sakura, Hiroshi, Otsuka, Kuniaki, Kobayashi, Hiroyuki
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 10.04.2015; Public Library of Science (PLoS)
• Subjects: Adrenergic receptors; Alleles; Animals; Augmented reality; Base Sequence; Bioinformatics; Blood flow; Brain; Diabetes; Disease; Dissociation; DNA - analysis; DNA - isolation & purification; DNA, Mitochondrial - analysis; DNA, Mitochondrial - classification; Epidemiology; Epinephrine - blood; Evolution; Evolution, Molecular; Female; Gene Frequency; Genes; Genetics; Genomes; Genotype; Genotypes; GTP-Binding Protein alpha Subunits, Gi-Go - metabolism; Heart failure; Humans; Kinases; Male; Molecular biology; Molecular interactions; Norepinephrine - blood; Pharmacology; Phylogeny; Polymorphism; Polymorphism, Single Nucleotide; Primates - genetics; Protein Binding; Protein Structure, Secondary; Protein Structure, Tertiary; Proteins; Receptors, Adrenergic, alpha-2 - chemistry; Receptors, Adrenergic, alpha-2 - genetics; Receptors, Adrenergic, alpha-2 - metabolism; Studies; Syncope; Syncope, Vasovagal - metabolism; Syncope, Vasovagal - pathology; Thermodynamics; Womens health; Japan
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0120788

The objective of this study was to clarify the effects of disease on neurally mediated syncope (NMS) during an acute stress reaction. We analyzed the mechanism of the molecular interaction and the polymorphisms of the alpha-2 adrenoreceptor (α2B-AR) gene as the potential psychiatric cause of incentive stress. We focused on the following three genotypes of the repeat polymorphism site at Glu 301-303 in the α2B-AR gene: Glu12/12, Glu12/9, and Glu9/9. On the basis of our clinical research, NMS is likely to occur in people with the Glu12/9 heterotype. To verify this, we assessed this relationship with the interaction of Gi protein and adenylate cyclase by in silico analysis of the Glu12/9 heterotype. By measuring the difference in the dissociation time of the Gi-α subunit twice, we found that the Glu12/9 heterotype suppressed the action of adenylate cyclase longer than the Glu homotypes. As this difference in the Glu repeat number effect is thought to be one of the causes of NMS, we investigated the evolutionary significance of the Glu repeat number. Glu8 was originally repeated in simians, while the Glu12 repeats occurred over time during the evolution of bipedalism in humans. Taken with the Glu12 numbers, NMS would likely become a defensive measure to prevent significant blood flow to the human brain.