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Firing Properties of Respiratory Rhythm Generating Neurons in the Absence of Synaptic Transmission in Rat Medulla in Vitro

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Journal Exp Brain Res
Specialty Neurology
Date 1989 Jan 1
PMID 2551710
Citations 34
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Abstract

It has previously been demonstrated that Pre-I neurons, localized in the rostral ventrolateral medulla, are important in the generation of the primary respiratory rhythm in brainstem-spinal cord preparations from newborn rats. To investigate whether or not Pre-I neurons have endogenous pacemaker properties, we examined Pre-I neuron activity before and after chemical synaptic transmission was blocked by incubation in a low Ca2+ (0.2 mM), high Mg2+ (5 mM) solution (referred to here as low Ca). After incubation for about 30 min in low Ca, 28 (52%, type-1) out of 54 neurons tested in 27 preparations retained apparent rhythmic (phasic) activity after complete disappearance of C4 inspiratory activity. Sixteen neurons (30%, type-2) fired tonically and 10 (18%, type-3) were silent. We examined the effects of synaptic blockade on 14 inspiratory neurons in the RVL. The firing of all 14 neurons in 9 preparations disappeared concomitantly with the disappearance of C4 activity in low Ca. When the pH of the low Ca solution was lowered with a decrease in NaHCO3 concentration from 7.4 to 7.1, the firing rate of the Pre-I neurons (type-1) increased from 12 to 18/min. In conclusion, the generator of respiratory rhythm in the newborn rat is probably a neuronal network with chemical synapses that functions mainly through the endogenous Pre-I pacemaker cells. Intrinsic chemoreception in the rhythm generator is probably important in frequency control of respiratory rhythm.

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References
1.
Fukuda Y, Loeschcke H . Effect of H+ on spontaneous neuronal activity in the surface layer of the rat medulla oblongata in vitro. Pflugers Arch. 1977; 371(1-2):125-34. DOI: 10.1007/BF00580780. View

2.
Onimaru H, Arata A, Homma I . Localization of respiratory rhythm-generating neurons in the medulla of brainstem-spinal cord preparations from newborn rats. Neurosci Lett. 1987; 78(2):151-5. DOI: 10.1016/0304-3940(87)90624-0. View

3.
Onimaru H, Arata A, Homma I . Primary respiratory rhythm generator in the medulla of brainstem-spinal cord preparation from newborn rat. Brain Res. 1988; 445(2):314-24. DOI: 10.1016/0006-8993(88)91194-8. View

4.
Cohen M . Neurogenesis of respiratory rhythm in the mammal. Physiol Rev. 1979; 59(4):1105-73. DOI: 10.1152/physrev.1979.59.4.1105. View

5.
Smith J, Feldman J . In vitro brainstem-spinal cord preparations for study of motor systems for mammalian respiration and locomotion. J Neurosci Methods. 1987; 21(2-4):321-33. DOI: 10.1016/0165-0270(87)90126-9. View