S. Nomoto et al., INFLUENCE OF HEPATIC MITOCHONDRIAL REDOX STATE ON COMPLEMENT BIOSYNTHESIS AND ACTIVATION DURING AND AFTER CARDIOPULMONARY BYPASS OPERATIONS, European journal of cardio-thoracic surgery, 10(4), 1996, pp. 273-278
We have proposed the hazardous phenomena associated with cardiopulmona
ry bypass (CPB) are due to metabolic derangement by hepatic mitochondr
ial dysfunction during and after CPB. On the contrary, complement acti
vation and consumption during CPB is reported to be related to the mor
bidity associated with cardiac surgery. To determine the significance
of the hepatic mitochondrial function on the morbidity of cardiac surg
ery, we measured the serum levels of complements (C3 and C4), activate
d complements (C3a and C4a), and the arterial ketone body ratio (AKBR)
, which reflects the hepatic mitochondrial redox state, in 30 patients
undergoing CPB. The AKBR, which was at a normal level preoperatively,
dropped to a critical level after the initiation of CPB and remained
at a low level during the CP8, returning to the preoperative level on
the second postoperative morning in a time dependent fashion. The pati
ents group were assigned to two groups according to their AKBR on the
first postoperative morning. Group I consisted of patients whose AKBR
had recovered to above 0.7 on the first postoperative morning (n=16).
Group II consisted of the rest of the patients (n=14). The serum compl
ement concentration had considerably decreased by the end of bypass, b
ut recovered in a time-dependent fashion after CPB, The group I patien
ts (C3: 71% of its preoperative value, C4: 85% of its preoperative val
ue) recovered their complements more quickly than the group II patient
s (C3: 56% of its preoperative value, C4: 54% of its preoperative valu
e). However, the serum C3a and C4a concentrations increased by the end
of bypass (C3a: 806% of its preoperative value, C4a: 341% of its preo
perative value). The activated complements were significantly higher i
n the group II patients (C3a: 124% of its preoperative value, C4a: 236
% of its preoperative value) than in the group I patients (C3a: 75% of
its preoperative value, C4a: 113% of its preoperative value) on the f
irst postoperative morning. It is suggested that hepatic mitochondrial
function is related to recovering the complements and to reducing the
activated complements after CPB.