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March 5, 2008Journal of Neuroscience321 citationsOpen Access

Defects in Breathing and Thermoregulation in Mice with Near-Complete Absence of Central Serotonin Neurons

MHMatthew R. HodgesGTGlenn J. TattersallMHMichael B. Harris

Key Result

Lmx1bf/f/p mice with near-complete absence of central serotonin neurons exhibited a 50% decrease in the hypercapnic ventilatory response and rapidly became hypothermic when exposed to 4°C.

Structured PICO

P
Population
n=133 mice (59 adult, 74 neonatal), including Lmx1b(f/f/p) conditional knock-out mice with near-complete absence of central 5-HT neurons and wild-type littermates.
I
Intervention
Genetic deletion of Lmx1b in Pet1-expressing cells (Lmx1b(f/f/p) mice) resulting in near-complete absence of central serotonin (5-HT) neurons. A subset received intracerebroventricular infusion of 5-HT.
C
Comparator
Wild-type (WT) littermates.
O
Outcome
Hypercapnic ventilatory response and core body temperature maintenance during cold exposure (4°C).surrogate

Central serotonin neurons play a critical role in the hypercapnic ventilatory response and thermoregulatory cold defense in mice.

Main Result

p-value: p=<0.05

Limitations

  • Experimental design did not allow evaluation of differences in respiratory control during sleep versus wakefulness
  • Intracerebroventricular 5-HT concentrations may be higher than physiological tissue levels
  • Experimental design did not allow evaluation of differences in the effects of 5-HT neuron loss on respiratory control during sleep versus wakefulness.
  • Inherent problems in ventilatory measurements in small mammals.

Abstract

Serotonergic neurons project widely throughout the CNS and modulate many different brain functions. Particularly important, but controversial, are the contributions of serotonin (5-HT) neurons to respiratory and thermoregulatory control. To better define the roles of 5-HT neurons in breathing and thermoregulation, we took advantage of a unique conditional knock-out mouse in which Lmx1b is genetically deleted in Pet1-expressing cells (Lmx1b(f/f/p)), resulting in near-complete absence of central 5-HT neurons. Here, we show that the hypercapnic ventilatory response in adult Lmx1b(f/f/p) mice was decreased by 50% compared with wild-type mice, whereas baseline ventilation and the hypoxic ventilatory response were normal. In addition, Lmx1b(f/f/p) mice rapidly became hypothermic when exposed to an ambient temperature of 4 degrees C, decreasing core temperature to 30 degrees C within 120 min. This failure of thermoregulation was caused by impaired shivering and nonshivering thermogenesis, whereas thermosensory perception and heat conservation were normal. Finally, intracerebroventricular infusion of 5-HT stimulated baseline ventilation, and rescued the blunted hypercapnic ventilatory response. These data identify a previously unrecognized role of 5-HT neurons in the CO(2) chemoreflex, whereby they enhance the response of the rest of the respiratory network to CO(2). We conclude that the proper function of the 5-HT system is particularly important under conditions of environmental stress and contributes significantly to the hypercapnic ventilatory response and thermoregulatory cold defense.

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Cite This Study

Hodges et al. (2008) studied Serotonin neuron deficiency (n=133). Lmx1b genetic deletion in Pet1-expressing cells (Lmx1bf/f/p) vs. Wild-type mice was evaluated on Hypercapnic ventilatory response (increase in minute ventilation during 5% CO2) (p=<0.05). Lmx1bf/f/p mice with near-complete absence of central serotonin neurons exhibited a 50% decrease in the hypercapnic ventilatory response and rapidly became hypothermic when exposed to 4°C.

synapsesocial.com/papers/6a110afa6f378c85fcf336b7https://doi.org/10.1523/jneurosci.4729-07.2008
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