Msw. Mahmoud et al., ATP-MGCL2 TREATMENT AFTER TRAUMA-HEMORRHAGE RESUSCITATION INCREASES HEPATOCYTE P-2-PURINOCEPTOR BINDING-CAPACITY, The American journal of physiology, 266(6), 1994, pp. 180001810-180001815
Although our studies indicate that P-2-purinoceptor binding capacity d
ecreases after hemorrhage and resuscitation, it is not known whether A
TP-MgCl2 administration after hemorrhage has any beneficial effects on
the receptor dynamics. To study this, we performed laparotomy (i.e.,
trauma induced) on rats and bled them to and maintained them at a mean
arterial pressure of 40 mmHg until 40% of maximum bleedout volume was
returned in the form of Ringer lactate (RL). The animals were then re
suscitated with 3 times the volume of maximum bleedout with RL over 45
min followed by 2 times RL along with ATP-MgCl2 (50 mu mol/kg body wt
) over 95 min. Hepatocytes were isolated at 4, 17, and 27 h after resu
scitation. P-2-purinoceptor binding characteristics were determined by
using [alpha-S-35]ATP. Scatchard analysis revealed high-affinity and
low-affinity receptor components in the hepatocytes isolated from sham
-operated or hemorrhaged animals with or without ATP-MgCl2 infusion. A
TP-MgCl2 ameliorated and subsequently restored the decreased maximum b
inding capacity (B-max) of the high-affinity receptor component and si
gnificantly improved B-max of the low-affinity receptor component. ATP
-MgCl2 administration also produced a progressive enhancement in the a
ffinity of the low-affinity receptor component. Thus the beneficial ef
fects of ATP-MgCl2 observed after trauma-hemorrhage and resuscitation
may be, in part, due to the restoration of P-2-purinoceptor binding ca
pacity and the enhancement of the receptor affinity.