Key result
Bilateral superior cervical ganglionectomy significantly attenuated the enhanced chemoreflex sensitivity in response to hypoxia and normoxic-hypercapnia during recovery from acute lung injury.
Why the study?
Chemoreflex is sensitized during recovery from acute lung injury, and the superior cervical ganglion was hypothesized to be involved in this sensitization.
Does bilateral superior cervical ganglionectomy attenuate chronic chemoreflex sensitization during recovery from acute lung injury in a rat model?
Does bilateral superior cervical ganglionectomy attenuate chronic chemoreflex sensitization during recovery from acute lung injury in a rat model?
p-value: p=<0.05
Bilateral superior cervical ganglionectomy attenuates chronic chemoreflex sensitization during recovery from acute lung injury in rats, suggesting the superior cervical ganglion plays a key role in this pathological reflex.
Hypothesis-generating for superior cervical ganglion's role in post-lung injury chemoreflex sensitization; does not support clinical translation.
Introduction: Acute lung injury (ALI) initiates an inflammatory cascade that impairs gas exchange, induces hypoxemia, and causes an increase in respiratory rate (f R ). This stimulates the carotid body (CB) chemoreflex, a fundamental protective reflex that maintains oxygen homeostasis. Our previous study indicated that the chemoreflex is sensitized during the recovery from ALI. The superior cervical ganglion (SCG) is known to innervate the CB, and its electrical stimulation has been shown to significantly sensitize the chemoreflex in hypertensive and normotensive rats. We hypothesized that the SCG is involved in the chemoreflex sensitization post-ALI. Methods: We performed a bilateral SCG ganglionectomy (SCGx) or sham-SCGx (Sx) in male Sprague Dawley rats 2 weeks before inducing ALI (Week −2 i.e., W-2). ALI was induced using a single intra-tracheal instillation of bleomycin (bleo) (day 1). Resting-f R , V t (Tidal Volume), and V̇ E (Minute Ventilation) were measured. The chemoreflex response to hypoxia (10% O 2 , 0% CO 2 ) and normoxic-hypercapnia (21% O 2 , 5% CO 2 ) were measured before surgery on W (−3), before bleo administration on W0 and on W4 post-bleo using whole-body plethysmography (WBP). Results: SCGx did not affect resting f R , V t and V̇ E as well as the chemoreflex responses to hypoxia and normoxic hypercapnia in either group prior to bleo. There was no significant difference in ALI-induced increase in resting f R between Sx and SCGx rats at W1 post-bleo. At W4 post-bleo, there were no significant differences in resting f R , V t , and V̇ E between Sx and SCGx rats. Consistent with our previous study, we observed a sensitized chemoreflex (delta f R ) in response to hypoxia and normoxic hypercapnia in Sx rats at W4 post-bleo. However, at the same time, compared to Sx rats, the chemoreflex sensitivity was significantly less in SCGx rats in response to either hypoxia or normoxic hypercapnia. Discussion: These data suggest that SCG is involved in the chemoreflex sensitization during ALI recovery. Further understanding of the underlying mechanism will provide important information for the long-term goal of developing novel targeted therapeutic approaches to pulmonary diseases to improve clinical outcomes.
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Kamra et al. (2023) studied Acute lung injury (n=18). Bilateral superior cervical ganglionectomy (SCGx) vs. Sham surgery (Sx) was evaluated on Chemoreflex sensitivity (delta respiratory rate) in response to hypoxia and normoxic hypercapnia at 4 weeks post-bleomycin (p=<0.05). Bilateral superior cervical ganglionectomy significantly attenuated the enhanced chemoreflex sensitivity in response to hypoxia and normoxic-hypercapnia during recovery from acute lung injury.
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