The α7 nicotinic acetylcholine receptor and the acute stress response: maternal genotype determines offspring phenotype
| Autor: | Tasha E. Fingerlin, Melissa L. Sinkus, Mark L. Laudenslager, Amanda Barton, Marianne Z. Wamboldt, Sherry Leonard |
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| Rok vydání: | 2010 |
| Předmět: |
Male
medicine.medical_specialty Adolescent Genotype Hydrocortisone alpha7 Nicotinic Acetylcholine Receptor Offspring Radioimmunoassay Experimental and Cognitive Psychology Receptors Nicotinic Article Atopy Behavioral Neuroscience Young Adult Gene Frequency Internal medicine medicine Humans Genetic Predisposition to Disease Receptor Child Saliva Polymorphism Genetic biology CHRNA7 Maternal effect Age Factors medicine.disease Mother-Child Relations Endocrinology Phenotype Immunology biology.protein Cholinergic Female Stress Psychological medicine.drug |
| Zdroj: | Physiologybehavior. 104(2) |
| ISSN: | 1873-507X |
| Popis: | α7 Nicotinic acetylcholine receptors (α7nAchRs) modulate immune activation by suppressing production of pro-inflammatory cytokines in peripheral immune cells. α7nAchRs also modulate inhibitory output in the hippocampus, which provides input to key circuits of the HPA axis. Therefore, the α7 nicotinic acetylcholine receptor gene (CHRNA7) may be associated with cortisol stress response. Polymorphisms in the CHRNA7 promoter decrease its expression and may dampen the cholinergic response, leading to an increase in inflammation. Increased inflammation may change the intrauterine environment, altering neuroendocrine development in the offspring. Maternal CHRNA7 genotype could affect an offspring's HPA regulation via reprogramming in utero. Patients with allergic disorders have a differential cortisol response to stress. This study utilized samples collected from a cohort of 198 adolescents in a previous study of atopic disorders, who demonstrated a disturbance in HPA response associated with atopy. Salivary cortisol samples collected from the adolescents after a series of laboratory procedures and DNA samples collected from the adolescents and their parents were used for further analysis. DNA samples were genotyped for allelic variation in the CHRNA7 promoter. Genetic association analyses with the cortisol levels were performed in the adolescents. Maternal genotype influences were investigated for the CHRNA7 gene. We also included maternal and child atopy diagnosis as covariates in determining cortisol levels and tested for association of CHRNA7 to atopy. Polymorphisms in the CHRNA7 promoter were associated with lower cortisol levels after a small laboratory stress. Our findings also show that although the child's CHRNA7 genotype affects stress response, the maternal genotype has a stronger influence on cortisol release after stress in male offspring. These effects were independent of atopy status. |
| Databáze: | OpenAIRE |
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