Rh. Coker et al., SYMPATHETIC DRIVE TO LIVER AND NONHEPATIC SPLANCHNIC TISSUE DURING HEAVY EXERCISE, Journal of applied physiology, 82(4), 1997, pp. 1244-1249
The contribution of sympathetic drive and vascular catecholamine deliv
ery to the splanchnic bed during heavy exercise was studied in dogs th
at underwent a laparotomy during which flow probes were implanted onto
the portal vein and hepatic artery and catheters were inserted into t
he carotid artery, portal vein, and hepatic vein. At least 16 days aft
er surgery, dogs completed a 20-min heavy exercise protocol (mean work
rate of 5.7 +/- 1 miles/h, 20 +/- 2% grade). Arterial epinephrine (Ep
i) and norepinephrine (NE) increased by similar to 500 and similar to
900 pg/ml, respectively, after 20 min of heavy exercise. Because Epi i
s not released from the splanchnic bed and because Epi fractional extr
action (FX) = NE FX, NE uptake by splanchnic tissue can be calculated
despite simultaneous release of NE. Basal nonhepatic splanchnic (NHS)
FX increased from a basal rate of 0.52 +/- 0.09 to a peak of 0.64 +/-
0.05 at 10 min of exercise. Hepatic Epi FX increased from a basal rate
of 0.68 +/- 0.10 to 0.81 +/- 0.09 at 20 min of exercise. Even though
NHS extraction of Epi reduced portal vein Epi levels by similar to 60%
, the release of NE from NHS tissue maintained portal vein NE; at leve
ls similar to those in arterial blood. NHS NE spillover increased from
a basal rate of 5.7 +/- 1.4 to 11.7 +/- 2.8 ng kg(-1) min(-1) at 20 m
in of exercise. Hepatic NE spillover increased from a basal rate of 5.
0 +/- 1.2 ng kg(-1) min(-1) to a peak of 14.2 +/- 2.8 ng kg(-1) min(-1
) at 15 min of exercise. These results show that I) approximately two-
and threefold increases in NHS and hepatic NE spillover occur during
heavy exercise, demonstrating that sympathetic drive to these tissues
contributes to the increase in circulating NE; 2) the high catecholami
ne FX by the NHS tissues results in an Epi level at the liver that is
considerably lower than that in the arterial blood; and 3) circulating
NE delivery to the liver is sustained despite high catecholamine FX d
ue to simultaneous NHS NE release.