TY - JOUR
T1 - Attenuation of renal ischemia-reperfusion injury by FR167653 in dogs
AU - Kitada, Hidehisa
AU - Sugitani, Atsushi
AU - Yamamoto, Hirofumi
AU - Otomo, Naoki
AU - Okabe, Yasuhiro
AU - Inoue, Shigetaka
AU - Nishiyama, Ken Ichi
AU - Morisaki, Takashi
AU - Tanaka, Masao
PY - 2002
Y1 - 2002
N2 - Background. Inflammatory cytokines are known to contribute to ischemia-reperfusion injury. We investigated the effect of FR167653 (FR), a suppressor of interleukin-1β and tumor necrosis factor-α, on ischemia-reperfusion injury of the kidney in dogs. Methods. The left kidney was subjected to ischemia for 60 minutes followed by removal of the right kidney. A control group (n = 10) and an FR group (n = 8) were evaluated for tissue blood flow; resistive index, pulsatility index, arterial oxygen pressure, serum creatinine, blood urea nitrogen, aspartate transaminase, and alanine transaminase levels; interleukin-1β messenger RNA expression in the peripheral blood; apoptotic index; and histopathology. Results. The FR group showed lower creatinine, serum urea nitrogen, aspartate transaminase, and alanine transaminase levels (P <.038 each) and lower interleukin-1β mRNA expression and apoptotic index (P <.041 each) than did the control group. Arterial oxygen pressure during the 120 minutes after reperfusion in the FR group decreased but recovered quickly (P =.024). Renal tissue damage in the FR group was less than that in the control group (P =.036). Conclusions. FR ameliorates ischemia-reperfusion injury of the kidney potentially by reduced production of inflammatory cytokines that may contribute to damage to the ischemic kidney and the distant organs.
AB - Background. Inflammatory cytokines are known to contribute to ischemia-reperfusion injury. We investigated the effect of FR167653 (FR), a suppressor of interleukin-1β and tumor necrosis factor-α, on ischemia-reperfusion injury of the kidney in dogs. Methods. The left kidney was subjected to ischemia for 60 minutes followed by removal of the right kidney. A control group (n = 10) and an FR group (n = 8) were evaluated for tissue blood flow; resistive index, pulsatility index, arterial oxygen pressure, serum creatinine, blood urea nitrogen, aspartate transaminase, and alanine transaminase levels; interleukin-1β messenger RNA expression in the peripheral blood; apoptotic index; and histopathology. Results. The FR group showed lower creatinine, serum urea nitrogen, aspartate transaminase, and alanine transaminase levels (P <.038 each) and lower interleukin-1β mRNA expression and apoptotic index (P <.041 each) than did the control group. Arterial oxygen pressure during the 120 minutes after reperfusion in the FR group decreased but recovered quickly (P =.024). Renal tissue damage in the FR group was less than that in the control group (P =.036). Conclusions. FR ameliorates ischemia-reperfusion injury of the kidney potentially by reduced production of inflammatory cytokines that may contribute to damage to the ischemic kidney and the distant organs.
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U2 - 10.1067/msy.2002.124629
DO - 10.1067/msy.2002.124629
M3 - Article
C2 - 12075178
AN - SCOPUS:0036082565
SN - 0039-6060
VL - 131
SP - 654
EP - 662
JO - Surgery
JF - Surgery
IS - 6
ER -