Experimental analysis shows hypercapnia reduces phrenic nerve activity during rest in rats, suggesting time-of-day influences physiological responses.
Phrenic long-term facilitation (pLTF) is a form of respiratory motor plasticity, expressed as a lasting increase in phrenic nerve activity following acute intermittent hypoxia (AIH). Whereas AIH also elicits ventilatory LTF (vLTF) in unanesthetized rats, concurrent hypercapnia (elevated background or episodic hypercapnia) is required for vLTF in humans. One major difference between rodent and human studies is the diurnal phase (nocturnal rats vs diurnal humans). Diurnal phase regulates pLTF magnitude and mechanism; 15, 1-minute hypoxic episodes elicit more robust pLTF in the rest (~130%) vs active phase (~30%) in rats. Thus, we assessed differences in pLTF elicited by acute intermittent hypercapnic-hypoxia (AIHH) vs AIH in mid-rest vs mid-active phase rats. In anesthetized, paralyzed, vagotomized and ventilated male Sprague-Dawley rats ( n=7 per group), pLTF was assessed following moderate AIH (arterial PO 2 range 35-49mmHg; 15, 1-min episodes) or AIHH (arterial PCO 2 range 46-50mmHg) in the mid-rest (noon) and mid-active phases (midnight). In contrast to expectations, mid-rest phase pLTF 90 min post AIHH (64±45%) was less than that elicited by AIH (132±93%; P<0.001). As reported previously, AIH-induced pLTF was lower in mid-active (46±47%; P=0.050) vs mid-rest rats; however, AIHH-induced pLTF was not significantly different in mid-rest vs mid-active phase rats (37±28%; P=0.20), and there was no longer a significant difference between AIH vs AIHH in the active phase (P=0.650). Thus, adding hypercapnia to an AIH protocol suppresses pLTF in anesthetized rats exclusively in the mid-rest, but not mid-active phase of the diurnal cycle. Possible mechanisms for hypercapnia and time-of-day effects are discussed.
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Butenas et al. (2025) studied this question.
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