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DNA methylation in the central and efferent limbs of the chemoreflex requires carotid body neural activity
Author(s) -
Nanduri Jayasri,
Peng YingJie,
Wang Ning,
Khan Shakil A.,
Semenza Gregg L.,
Prabhakar Nanduri R.
Publication year - 2018
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jp274833
Subject(s) - endocrinology , dna methylation , medicine , chemistry , dnmt1 , methylation , reactive oxygen species , intermittent hypoxia , microbiology and biotechnology , gene expression , biology , biochemistry , gene , obstructive sleep apnea
Key points The mechanisms underlying long‐term (30 days) intermittent hypoxia (LT‐IH)‐evoked DNA methylation of anti‐oxidant enzyme (AOE) gene repression in the carotid body (CB) reflex pathway were examined. LT‐IH‐treated rats showed increased reactive oxygen species (ROS) levels in the CB reflex pathway. Administration of a ROS scavenger or CB ablation blocked LT‐IH‐evoked DNA methylation and AOE gene repression in the central and efferent limbs of the CB reflex. LT‐IH increased DNA methyltransferase (Dnmt) activity through upregulation of Dnmt1 and 3b proteins by ROS‐dependent inactivation of glycogen synthase kinase 3β (GSK3β) by Akt. A pan‐Akt inhibitor prevented LT‐IH‐induced GSK3β inactivation, elevated Dnmt protein expression and activity, AOE gene methylation, sympathetic activation and hypertension.Abstract Long‐term exposure to intermittent hypoxia (LT‐IH; 30 days), simulating blood O 2 profiles during sleep apnoea, has been shown to repress anti‐oxidant enzyme (AOE) gene expression by DNA methylation in the carotid body (CB) reflex pathway, resulting in persistent elevation of plasma catecholamine levels and blood pressure. The present study examined the mechanisms by which LT‐IH induces DNA methylation. Adult rats exposed to LT‐IH showed elevated reactive oxygen species (ROS) in the CB, nucleus tractus solitarius (nTS) and rostroventrolateral medulla (RVLM) and adrenal medulla (AM), which represent the central and efferent limbs of the CB reflex, respectively. ROS scavenger treatment during the first ten days of IH exposure prevented ROS accumulation, blocked DNA methylation, and normalized AOE gene expression, suggesting that ROS generated during the early stages of IH activate DNA methylation. CB ablation prevented the ROS accumulation, normalized AOE gene expression in the nTS, RVLM, and AM and blocked DNA methylation, suggesting that LT‐IH‐induced DNA methylation in the central and efferent limbs of the CB reflex is indirect and requires CB neural activity. LT‐IH increased DNA methyl transferase (Dnmt) activity through upregulation of Dnmt1 and 3b protein expression due to ROS‐dependent inactivation of glycogen synthase kinase 3β (GSK3β) by protein kinase B (Akt). Treating rats with the pan‐Akt inhibitor GSK690693 blocked the induction of Dnmt activity, Dnmt protein expression, and DNA methylation, leading to normalization of AOE gene expression as well as plasma catecholamine levels and blood pressure.