Organization of the core respiratory network: Insights from optogenetic and modeling studies

被引:46
作者
Ausborn, Jessica [1 ]
Koizumi, Hidehiko [2 ]
Barnett, William H. [3 ]
John, Tibin T. [2 ]
Zhang, Ruli [2 ]
Molkov, Yaroslav, I [3 ]
Smith, Jeffrey C. [2 ]
Rybak, Ilya A. [1 ]
机构
[1] Drexel Univ, Coll Med, Dept Neurobiol & Anat, Philadelphia, PA 19104 USA
[2] NINDS, Cellular & Syst Neurobiol Sect, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA
[3] Georgia State Univ, Dept Math & Stat, Atlanta, GA 30303 USA
基金
美国国家卫生研究院;
关键词
PRE-BOTZINGER COMPLEX; DECREMENTING EXPIRATORY NEURONS; CENTRAL PATTERN GENERATOR; MAMMALIAN BRAIN-STEM; RHYTHM GENERATION; PACEMAKER NEURONS; VENTROLATERAL MEDULLA; PREBOTZINGER COMPLEX; IN-VITRO; FUNCTIONAL ARCHITECTURE;
D O I
10.1371/journal.pcbi.1006148
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The circuit organization within the mammalian brainstem respiratory network, specifically within and between the pre-Botzinger (pre-BotC) and Botzinger (BotC) complexes, and the roles of these circuits in respiratory pattern generation are continuously debated. We address these issues with a combination of optogenetic experiments and modeling studies. We used transgenic mice expressing channelrhodopsin-2 under the VGAT-promoter to investigate perturbations of respiratory circuit activity by site-specific photostimulation of inhibitory neurons within the pre-BotC or BotC. The stimulation effects were dependent on the intensity and phase of the photostimulation. Specifically: (1) Low intensity (<= 1.0 mW) pulses delivered to the pre-BotC during inspiration did not terminate activity, whereas stronger stimulations (>= 2.0 mW) terminated inspiration. (2) When the pre-BotC stimulation ended in or was applied during expiration, rebound activation of inspiration occurred after a fixed latency. (3) Relatively weak sustained stimulation (20 Hz, 0.5-2.0 mW) of pre-BotC inhibitory neurons increased respiratory frequency, while a further increase of stimulus intensity (> 3.0 mW) reduced frequency and finally (>= 5.0 mW) terminated respiratory oscillations. (4) Single pulses (0.2-5.0 s) applied to the BotC inhibited rhythmic activity for the duration of the stimulation. (5) Sustained stimulation (20 Hz, 0.5-3.0 mW) of the BotC reduced respiratory frequency and finally led to apnea. We have revised our computational model of pre-BotC and BotC microcircuits by incorporating an additional population of post-inspiratory inhibitory neurons in the pre-BotC that interacts with other neurons in the network. This model was able to reproduce the above experimental findings as well as previously published results of optogenetic activation of pre-BotC or BotC neurons obtained by other laboratories. The proposed organization of pre-BotC and BotC circuits leads to testable predictions about their specific roles in respiratory pattern generation and provides important insights into key circuit interactions operating within brainstem respiratory networks.
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页数:41
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