Functional knockout of the TRPV1 channel has no effect on the exercise pressor reflex in rats

The role played by the transient receptor potential vanilloid 1 (TRPV1) channel on the thin fibre afferents evoking the exercise pressor reflex is controversial. To shed light on this controversy, we compared the exercise pressor reflex between newly developed TRPV1(+/+), TRPV1(+/-) and TRPV1(-/-) rats. Carotid arterial injection of capsaicin (0.5 mu g), evoked significant pressor responses in TRPV1(+/+) and TRPV1(+/-) rats, but not in TRPV1(-/-) rats. In acutely isolated dorsal root ganglion neurons innervating the gastrocnemius muscles, capsaicin evoked inward currents in neurons isolated from TRPV1(+/+) and TRPV1(+/-) rats but not in neurons isolated from TRPV1(-/-) rats. The reflex was evoked by stimulating the tibial nerve in decerebrated rats whose femoral artery was either freely perfused or occluded. We found no difference between the reflex in the three groups of rats regardless of the patency of the femoral artery. For example, the peak pressor responses to contraction in TRPV1(+/+), TRPV1(+/-) and TRPV1(-/-) rats with patent femoral arteries averaged 17.1 +/- 7.2, 18.9 +/- 12.4 and 18.4 +/- 8.6 mmHg, respectively. Stimulation of the tibial nerve after paralysis with pancuronium had no effect on arterial pressure, findings which indicated that the pressor responses to contraction were not caused by electrical stimulation of afferent tibial nerve axons. We also found that expression levels of acid-sensing ion channel 1 and endoperoxide 4 receptor in the L4 and 5 dorsal root ganglia were not upregulated in the TRPV1(-/-) rats. We conclude that TRPV1 is not needed to evoke the exercise pressor reflex in rats whose contracting muscles have either a patent or an occluded arterial blood supply.