» Articles » PMID: 32086251

Loss of Cerebellar Function Selectively Affects Intrinsic Rhythmicity of Eupneic Breathing

Overview
Journal Biol Open
Specialty Biology
Date 2020 Feb 23
PMID 32086251
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Respiration is controlled by central pattern generating circuits in the brain stem, whose activity can be modulated by inputs from other brain areas to adapt respiration to autonomic and behavioral demands. The cerebellum is known to be part of the neuronal circuitry activated during respiratory challenges, such as hunger for air, but has not been found to be involved in the control of spontaneous, unobstructed breathing (eupnea). Here we applied a measure of intrinsic rhythmicity, the CV2, which evaluates the similarity of subsequent intervals and is thus sensitive to changes in rhythmicity at the temporal resolution of individual respiratory intervals. The variability of intrinsic respiratory rhythmicity was reduced in a mouse model of cerebellar ataxia compared to their healthy littermates. Irrespective of that difference, the average respiratory rate and the average coefficient of variation (CV) were comparable between healthy and ataxic mice. We argue that these findings are consistent with a proposed role of the cerebellum in modulating the duration of individual respiratory intervals, which could serve the purpose of coordinating respiration with other rhythmic orofacial movements, such as fluid licking and swallowing.

Citing Articles

SubSol-HIe is an AMPK-dependent hypoxia-responsive subnucleus of the nucleus tractus solitarius that coordinates the hypoxic ventilatory response and protects against apnoea in mice.

MacMillan S, Burns D, OHalloran K, Mark Evans A Pflugers Arch. 2024; 476(7):1087-1107.

PMID: 38635058 PMC: 11166843. DOI: 10.1007/s00424-024-02957-6.


Purkinje cell dysfunction causes disrupted sleep in ataxic mice.

Salazar Leon L, Brown A, Kaku H, Sillitoe R Dis Model Mech. 2024; 17(6).

PMID: 38563553 PMC: 11190574. DOI: 10.1242/dmm.050379.


Transgenic rodents as dynamic models for the study of respiratory rhythm generation and modulation: a scoping review and a bibliometric analysis.

Olmos-Pastoresa C, Vazquez-Mendoza E, Lopez-Meraz M, Perez-Estudillo C, Beltran-Parrazal L, Morgado-Valle C Front Physiol. 2024; 14:1295632.

PMID: 38179140 PMC: 10764557. DOI: 10.3389/fphys.2023.1295632.


The integrated brain network that controls respiration.

Krohn F, Novello M, van der Giessen R, De Zeeuw C, Pel J, Bosman L Elife. 2023; 12.

PMID: 36884287 PMC: 9995121. DOI: 10.7554/eLife.83654.


Forebrain control of breathing: Anatomy and potential functions.

Schottelkotte K, Crone S Front Neurol. 2022; 13:1041887.

PMID: 36388186 PMC: 9663927. DOI: 10.3389/fneur.2022.1041887.


References
1.
Ebert D, Hefter H, Dohle C, Freund H . Ataxic breathing during alternating forearm movements of various frequencies in cerebellar patients. Neurosci Lett. 1995; 193(3):145-8. DOI: 10.1016/0304-3940(95)11674-l. View

2.
Asanuma C, Thach W, Jones E . Brainstem and spinal projections of the deep cerebellar nuclei in the monkey, with observations on the brainstem projections of the dorsal column nuclei. Brain Res. 1983; 286(3):299-322. DOI: 10.1016/0165-0173(83)90017-6. View

3.
Teune T, Van der Burg J, van der Moer J, Voogd J, Ruigrok T . Topography of cerebellar nuclear projections to the brain stem in the rat. Prog Brain Res. 2000; 124:141-72. DOI: 10.1016/S0079-6123(00)24014-4. View

4.
Holt G, Softky W, Koch C, Douglas R . Comparison of discharge variability in vitro and in vivo in cat visual cortex neurons. J Neurophysiol. 1996; 75(5):1806-14. DOI: 10.1152/jn.1996.75.5.1806. View

5.
Bryant J, Boughter J, Gong S, Ledoux M, Heck D . Cerebellar cortical output encodes temporal aspects of rhythmic licking movements and is necessary for normal licking frequency. Eur J Neurosci. 2010; 32(1):41-52. PMC: 4454453. DOI: 10.1111/j.1460-9568.2010.07244.x. View