Effects of chronic exposure to low dose THIP on brainstem neuronal excitability in mouse models of Rett syndrome: Evidence from symptomatic females. (April 2017)
- Record Type:
- Journal Article
- Title:
- Effects of chronic exposure to low dose THIP on brainstem neuronal excitability in mouse models of Rett syndrome: Evidence from symptomatic females. (April 2017)
- Main Title:
- Effects of chronic exposure to low dose THIP on brainstem neuronal excitability in mouse models of Rett syndrome: Evidence from symptomatic females
- Authors:
- Zhong, Weiwei
Johnson, Christopher Mychal
Cui, Ningren
Xing, Hao
Wu, Yang
Jiang, Chun - Abstract:
- Abstract: Rett Syndrome (RTT) is a neurodevelopmental disorder caused by mutations of the MECP2 gene, affecting predominantly females. One of the characteristic features of the disease is defective brainstem autonomic function. In Mecp2 −/Y mice, several groups of brainstem neurons are overly excitable, which causes destabilization of neuronal networks for the autonomic control. We have previously shown that the extrasynaptic GABAA receptor agonist THIP relieves many RTT-like symptoms in Mecp2 −/Y mice. Although neuronal activity is inhibited by acute THIP exposure, how a chronic treatment affects neuronal excitability remains elusive. Thus, we performed studies to address whether increased excitability occurs in brainstem neurons of female Mecp2 +/− mice, how the MeCP expression affects the neuronal excitability, and whether chronic THIP exposure improves the neuronal hyperexcitability. Symptomatic Mecp2 +/− (s Mecp2 +/− ) female mice were identified with a two-step screening system. Whole-cell recording was performed in brain slices after a prior exposure of the s Mecp2 +/− mice to a 5-week low-dose THIP. Neurons in the locus coeruleus (LC) and the mesencephalic trigeminal nucleus (Me5) showed excessive firing activity in the s Mecp2 +/− mice. THIP pretreatment reduced the hyperexcitability of both LC and Me5 neurons in the s Mecp2 +/− mice, to a similar level as their counterparts in Mecp2 −/Y mice. In identified LC neurons, the hyperexcitability appeared to be determinedAbstract: Rett Syndrome (RTT) is a neurodevelopmental disorder caused by mutations of the MECP2 gene, affecting predominantly females. One of the characteristic features of the disease is defective brainstem autonomic function. In Mecp2 −/Y mice, several groups of brainstem neurons are overly excitable, which causes destabilization of neuronal networks for the autonomic control. We have previously shown that the extrasynaptic GABAA receptor agonist THIP relieves many RTT-like symptoms in Mecp2 −/Y mice. Although neuronal activity is inhibited by acute THIP exposure, how a chronic treatment affects neuronal excitability remains elusive. Thus, we performed studies to address whether increased excitability occurs in brainstem neurons of female Mecp2 +/− mice, how the MeCP expression affects the neuronal excitability, and whether chronic THIP exposure improves the neuronal hyperexcitability. Symptomatic Mecp2 +/− (s Mecp2 +/− ) female mice were identified with a two-step screening system. Whole-cell recording was performed in brain slices after a prior exposure of the s Mecp2 +/− mice to a 5-week low-dose THIP. Neurons in the locus coeruleus (LC) and the mesencephalic trigeminal nucleus (Me5) showed excessive firing activity in the s Mecp2 +/− mice. THIP pretreatment reduced the hyperexcitability of both LC and Me5 neurons in the s Mecp2 +/− mice, to a similar level as their counterparts in Mecp2 −/Y mice. In identified LC neurons, the hyperexcitability appeared to be determined by not only the MeCP2 expression, but also their environmental cues. The alleviation of LC neuronal hyperexcitability seems to benefit brainstem autonomic function as THIP also improved breathing abnormalities of these s Mecp2 +/− mice. Highlights: Chronic treatment of THIP reduced the neuronal hyperexcitability of both locus coeruleus (LC) and the mesencephalic trigeminal nucleus (Me5) in symptomatic Mecp2 +/− (s Mecp2 +/− ) female mice. In identified LC neurons, the hyperexcitability appeared to be determined by not only the MeCP2 expression, but also their environmental cues. The alleviation of LC neuronal hyperexcitability may benefit brainstem autonomic function as THIP also improved breathing abnormalities of s Mecp2 +/− mice. … (more)
- Is Part Of:
- Neuropharmacology. Volume 116(2017)
- Journal:
- Neuropharmacology
- Issue:
- Volume 116(2017)
- Issue Display:
- Volume 116, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 116
- Issue:
- 2017
- Issue Sort Value:
- 2017-0116-2017-0000
- Page Start:
- 288
- Page End:
- 299
- Publication Date:
- 2017-04
- Subjects:
- Mecp2 -- Female mouse model -- THIP -- Electrophysiology -- Neuronal excitability -- Locus coeruleus
Neuropsychopharmacology -- Periodicals
Autonomic Agents -- Periodicals
Neuropsychopharmacologie -- Périodiques
Neuropsychopharmacology
Periodicals
Electronic journals
615.78 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00283908 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuropharm.2017.01.002 ↗
- Languages:
- English
- ISSNs:
- 0028-3908
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.517500
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