Serotonin-Mediated Cardiac Analgesia via Ah-Type Baroreceptor Activation Contributes to Silent Angina and Asymptomatic Infarction. (15th July 2019)
- Record Type:
- Journal Article
- Title:
- Serotonin-Mediated Cardiac Analgesia via Ah-Type Baroreceptor Activation Contributes to Silent Angina and Asymptomatic Infarction. (15th July 2019)
- Main Title:
- Serotonin-Mediated Cardiac Analgesia via Ah-Type Baroreceptor Activation Contributes to Silent Angina and Asymptomatic Infarction
- Authors:
- Wen, Xin
Yu, Xue
Huo, Rong
Yan, Qiu-Xin
Wu, Di
Feng, Yan
Li, Ying
Sun, Xun
Li, Xin-Yu
Sun, Jie
Li, Ke-Xin
Li, Qing-Yuan
Han, Li-Min
Lu, Xiao-Long
Liu, Yang
Shou, Weinian
Li, Bai-Yan - Abstract:
- Abstract: Silent angina is a critical phenomenon in the clinic and is more commonly associated with women patients suffering from myocardial ischemia. Its underlying cause remains mysterious in medicine. With our recent discovery of female-specific Ah-type baroreceptor neurons (BRNs), we hypothesize that cardiac analgesia is due to the direct activation of Ah-type BRNs by elevated levels of circulating serotonin (5-HT) myocardial infarction (MI) patients. Electromyography and the tail-flick reflex were assessed in control and MI-model rats to evaluate 5-HT-mediated BP regulation as well as peripheral and cardiac nociception. 5-HT or a 5-HT receptor agonist was microinjected into the nodose ganglion to confirm the involvement of the afferent pathway of the baroreflex arc. An inward current was observed in identified BRNs by applying a whole-cell patch-clamp technique in conjunction with qRT-PCR to verify the afferent-specific action of 5-HT and the expression of 5-HT receptors. Although the tail-flick reflex and mean arterial pressure were dramatically reduced in female MI rats with elevated serum 5-HT, intrapericardial capsaicin-evoked muscular discharges were significantly inhibited in comparing with those of males, which were mimicked by microinjection of 5-HT or SR57227A into the nodose. Ah-type BRNs displayed robust inward currents at lower concentrations of 5-HT than the C-type or the A-type, with significantly increased expression and cellular distribution of 5-HT3A RAbstract: Silent angina is a critical phenomenon in the clinic and is more commonly associated with women patients suffering from myocardial ischemia. Its underlying cause remains mysterious in medicine. With our recent discovery of female-specific Ah-type baroreceptor neurons (BRNs), we hypothesize that cardiac analgesia is due to the direct activation of Ah-type BRNs by elevated levels of circulating serotonin (5-HT) myocardial infarction (MI) patients. Electromyography and the tail-flick reflex were assessed in control and MI-model rats to evaluate 5-HT-mediated BP regulation as well as peripheral and cardiac nociception. 5-HT or a 5-HT receptor agonist was microinjected into the nodose ganglion to confirm the involvement of the afferent pathway of the baroreflex arc. An inward current was observed in identified BRNs by applying a whole-cell patch-clamp technique in conjunction with qRT-PCR to verify the afferent-specific action of 5-HT and the expression of 5-HT receptors. Although the tail-flick reflex and mean arterial pressure were dramatically reduced in female MI rats with elevated serum 5-HT, intrapericardial capsaicin-evoked muscular discharges were significantly inhibited in comparing with those of males, which were mimicked by microinjection of 5-HT or SR57227A into the nodose. Ah-type BRNs displayed robust inward currents at lower concentrations of 5-HT than the C-type or the A-type, with significantly increased expression and cellular distribution of 5-HT3A R but not 5-HT3B R compared to the A- and C-types. Activation of 5-HT3A R in Ah-type BRNs by 5-HT contributes significantly to cardiac analgesia, which may suggest the pathogenic condition that silent angina occurs mainly in female patients. Highlights: 5-HT mediates direct baroreflex activation leading to descending cardiac analgesia and inversed peripheral nociception. High sensitivity to 5-HT & up-regulated 5-HT3A R in female-specific Ah-BRN are cellular mechanism of baroreflex activation. Estrogen-dependent high level of serum 5-HT & 5-HT3A R expressed in Ah-BRN leads to sex difference of cardiac nociception. Higher 5-HT3B R expression is likely to explain why no or less sensitivity to 5-HT is observed in A- and C-BRN. Clinical relevance of these findings impacts on a gender difference in silent angina and asymptomatic cardiac infarction. … (more)
- Is Part Of:
- Neuroscience. Volume 411(2019)
- Journal:
- Neuroscience
- Issue:
- Volume 411(2019)
- Issue Display:
- Volume 411, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 411
- Issue:
- 2019
- Issue Sort Value:
- 2019-0411-2019-0000
- Page Start:
- 150
- Page End:
- 163
- Publication Date:
- 2019-07-15
- Subjects:
- serotonin (5-hydroxytryptamine, 5-HT) -- Baroreflex -- blood pressure -- silent angina -- myocardial infarction (MI) -- electromyography (EMG)
Neurochemistry -- Periodicals
Neurophysiology -- Periodicals
Neurology -- Periodicals
Neurochimie -- Périodiques
Neurophysiologie -- Périodiques
Neurochemistry
Neurophysiology
Electronic journals
Periodicals
Electronic journals
612.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03064522 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03064522 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03064522 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuroscience.2019.05.045 ↗
- Languages:
- English
- ISSNs:
- 0306-4522
- Deposit Type:
- Legaldeposit
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