Lq. Wang et al., REARTERIALIZATION OF LIVER-TUMORS AFTER VARIOUS DEARTERIALIZATION PROCEDURES, The Journal of surgical research, 57(4), 1994, pp. 454-459
Repeat dearterializations seem to be a means to prevent collateral for
mation, which is partly responsible for the failure of hepatic artery
ligation (HAL) or permanent dearterialization when used to treat liver
tumors. In this study restoration of tumor blood flow was evaluated a
fter various procedures: HAL (n = 12), permanent dearterialization (n
= 18), repeated dearterializations for 2 hr/day (n = 12), and sham dea
rterialization (n = 12). Tumor blood flow was measured 10 days after s
ham dearterialization, permanent dearterialization, and repeated deart
erializations for 2 hr in order to further illustrate the effect of pr
olonged dearterialization on tumor rearterialization. Hepatic and tumo
r arterial blood flow was measured using the reference organ method (N
EN, Ce-141 microspheres with diameter 15 mu m). Our results showed tha
t during a transient dearterialization blood flow decreased to 1% (0.0
1 +/- 0.01 ml/min/g) of the flow in the controls (0.82 +/- 0.10 ml/min
/g) (P < 0.01). After HAL tumor blood flow recovered to initial levels
after 48 hr (0.73 +/- 0.17 ml/min/g. Even in rats subjected to a perm
anent dearterialization blood flow was reestablished at Day 6 (0.59 +/
- 0.21 ml/min/g). In contrast, after repeat daily 2-hr dearterializati
ons blood flow remained significantly very low during the 6th transien
t dearterialization (0.11 +/- 0.03 ml/min/g) compared with both sham-o
peration and HAL as well as permanent dearterialization (P < 0.01). Du
ring the 10th daily dearterialization tumor blood flow was still signi
ficantly low compared with both controls (P < 0.001) and permanent dea
rterialization (P < 0.05). Our results indicate that both HAL and perm
anent dearterialization are inefficient to prevent rearterialization o
f tumor, although permanent dearterialization may keep blood flow redu
ced for a few days. However, repeat dearterializations significantly d
elay tumor growth and prevent tumor rearterialization for a prolonged
period. (C) 1994 Academic Press, Inc.