Preserving hepatic artery flow during portal triad blood inflow occlusion reduces the outgrowth of hepatocarcinoma in mice after ischemia-reperfusion

2013 ◽  
Vol 44 (12) ◽  
pp. 1224-1233 ◽  
Author(s):  
Bin Shi ◽  
Chong Hui Li ◽  
Yong Wei Chen ◽  
Shi Zhong Yang ◽  
Ai Qun Zhang ◽  
...  
Keyword(s):  
Hepatic Artery ◽  
Ischemia Reperfusion ◽  
Portal Triad ◽  
Inflow Occlusion ◽  
Blood Inflow ◽  
Artery Flow

Preserving Hepatic Artery Flow During Portal Triad Blood Inflow Occlusion Reduces Liver Ischemia-Reperfusion Injury in Rats

2012 ◽  
Vol 174 (1) ◽  
pp. 150-156 ◽  
Author(s):  
Yong Wei Chen ◽  
Chong Hui Li ◽  
Ai Qun Zhang ◽  
Shi Zhong Yang ◽  
Wen Zhi Zhang ◽  
...  
Keyword(s):  
Reperfusion Injury ◽  
Hepatic Artery ◽  
Ischemia Reperfusion Injury ◽  
Ischemia Reperfusion ◽  
Liver Ischemia ◽  
Portal Triad ◽  
Inflow Occlusion ◽  
Blood Inflow ◽  
Artery Flow

Preserving hepatic artery flow during portal triad blood inflow occlusion improves remnant liver regeneration in rats after partial hepatectomy

2013 ◽  
Vol 181 (2) ◽  
pp. 329-336 ◽  
Author(s):  
Peng Fei Wang ◽  
Chong Hui Li ◽  
Yong Wei Chen ◽  
Ai Qun Zhang ◽  
Shou Wang Cai ◽  
...  
Keyword(s):  
Liver Regeneration ◽  
Hepatic Artery ◽  
Partial Hepatectomy ◽  
Remnant Liver ◽  
Portal Triad ◽  
Inflow Occlusion ◽  
Blood Inflow ◽  
Artery Flow

Hemodynamic interaction between portal vien and hepatic artery flow in small-for-size split liver transplantation

2002 ◽  
Vol 15 (7) ◽  
pp. 355-360 ◽  
Author(s):  
Vassilios Smyrniotis ◽  
Georgia Kostopanagiotou ◽  
Agathi Kondi ◽  
Evangelos Gamaletsos ◽  
Kassiani Theodoraki ◽  
...  
Keyword(s):  
Liver Transplantation ◽  
Hepatic Artery ◽  
Split Liver Transplantation ◽  
Split Liver ◽  
Small For Size ◽  
Artery Flow

scholarly journals Preconditioning with L-alanyl-glutamine reduces hepatic ischemia-reperfusion injury in rats

2011 ◽  
Vol 26 (suppl 1) ◽  
pp. 8-13 ◽  
Author(s):  
Raimundo José Cunha Araújo Júnior ◽  
Raimundo Gerônimo da Silva Júnior ◽  
Marcelo Pinho Pessoa de Vasconcelos ◽  
Sérgio Botelho Guimarães ◽  
Paulo Roberto Leitão de Vasconcelos ◽  
...  
Keyword(s):  
Caspase 3 ◽  
Ischemia Reperfusion Injury ◽  
Ischemia Reperfusion ◽  
Control Group ◽  
Average Weight ◽  
Sham Operation ◽  
Hepatic Ischemia ◽  
Portal Triad ◽  
Hepatic Ischemia Reperfusion ◽  
Control Sham

PURPOSE: To evaluate the effects of pre-conditioning with L-alanyl- glutamine (L-Ala-Gln) in rats subjected to total hepatic ischemia. METHODS: Thirty Wistar rats, average weight 300g, were randomly assigned to 3 groups (n=10): G-1 - Saline, G-2- L-Ala-Gln, G-3-control (Sham). G-1 and G-3 groups were treated with saline 2.0 ml or L-Ala-Gln (0.75mg/Kg) intraperitoneally (ip) respectively, 2 hours before laparotomy. Anesthetized rats were subjected to laparotomy and total hepatic ischemia (30 minutes) induced by by clamping of portal triad. Control group underwent peritoneal puncture, two hours before the sham operation (laparotomy only). At the end of ischemia (G1 and G2), the liver was reperfused for 60 minutes. Following reperfusion blood samples were collected for evaluation of alanine aminotransferase (ALT) and lactate dehydrogenase (LDH) levels. Liver (medium lobe) was removed for immunohistochemistry study with antibody for Caspase-3. RESULTS: It was found a significant decrease (p<0.05) of ALT levels (270.6 +40.8 vs 83.3 +5.5 - p <0.05), LDH (2079.0 +262.4 vs. 206.6 +16.2 - p <0.05) and Caspase-3 expression (6.72 +1.35 vs. 2.19 +1.14, p <0.05) in rats subjected to I / R, comparing the group treated with L-Ala -Gln with G-2. Also, the ALT level was significantly lower (P<0.05) in G-1 and G-2 groups than in G-3 (control group). CONCLUSION: L-Ala-Gln preconditioning in rats submitted to hepatic I/R significantly reduces ALT, LDH and Caspase-3 expression, suggesting hepatic protection.

scholarly journals Intraportal versus Systemic Pentoxifylline Infusion after Normothermic Liver Ischemia: Effects on Regional Blood Flow Redistribution and Hepatic Ischemia-Reperfusion Injury

HPB Surgery ◽  
2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Edson A. Ribeiro ◽  
Luiz F. Poli-de-Figueiredo ◽  
Rodrigo Vincenzi ◽  
Flavio H. F. Galvao ◽  
Nelson Margarido ◽  
...  
Keyword(s):  
Blood Flow ◽  
Ischemia Reperfusion Injury ◽  
Regional Blood Flow ◽  
Ischemia Reperfusion ◽  
Microcirculatory Blood Flow ◽  
Hepatic Ischemia ◽  
Portal Triad ◽  
Beneficial Effects ◽  
Hepatic Ischemia Reperfusion ◽  
Blood Flow Redistribution

Pentoxifylline (PTX) has been shown to have beneficial effects on microcirculatory blood flow. In this study we evaluate the potential hemodynamic and metabolic benefits of PTX during hepatic ischemia. We also test the hypothesis that portal PTX infusion can minimize the I/R injury when compared to systemic infusion. Methods. Twenty-four dogs ( kg) were subjected to portal triad occlusion (PTO) for 45 min. The animals were assigned to 3 groups: CT (control, PTO, ), PTX-syst (PTO + 25 mg/Kg of PTX IV, ), and PTX-pv (PTO + 25 mg/Kg of PTX in the portal vein, ). Animals were followed for 120 min. Systemic hemodynamics, gastrointestinal tract perfusion, oxygen-derived variables, and liver enzymes were evaluated throughout the experiment. Results. Animals treated with PTX presented significantly higher CO in the first hour after reperfusion, when compared to the CT (~3.7 vs. 2.1 L/min, ). Alanine aminotransferase (ALT) was similar in the PTX groups two hours after reperfusion but significantly higher in the CT (227 vs. ~64 U/L, ). Conclusion. PTX infusion was associated with hemodynamic benefits and was able to minimize liver injury during normothermic hepatic I/R. However, local PTX infusion was not associated with any significant advantage over systemic route.

The Effects of Meclofenamate, Captopril and Phentolamine on Organ Blood Flow in the Conscious Rabbit

1981 ◽  
Vol 61 (1) ◽  
pp. 97-105 ◽  
Author(s):  
R. A. Banks ◽  
L. J. Beilin
Keyword(s):  
Blood Flow ◽  
Arterial Pressure ◽  
Hepatic Artery ◽  
Peripheral Resistance ◽  
Prostaglandin Synthesis ◽  
Organ Blood Flow ◽  
Inhibit Prostaglandin Synthesis ◽  
Conscious Rabbits ◽  
Artery Flow ◽  
Intravenous Sodium

1. Systemic and regional vascular changes were measured in conscious rabbits after intravenous sodium meclofenamate, captopril and phentolamine. These drugs were used respectively to inhibit prostaglandin synthesis and angiotensin-converting enzyme, and to block α-adrenoceptors. 2. Meclofenamate reduced renal and adrenal blood flow by 11 and 28% respectively, and doubled hepatic artery flow. The effect on renal and adrenal flow persisted in the presence of phentolamine. 3. Captopril decreased estimated peripheral resistance and increased cardiac output without changing arterial pressure. Kidney and adrenal flow increased by 70 and 21% respectively. 4. Phentolamine reduced arterial pressure and doubled flow to skeletal muscle and increased hepatic artery flow to the liver. 5. Splenic blood flow was unaffected by meclofenamate, captopril or phentolamine alone. Meclofenamate given after captopril caused a halving of splenic flow and a rise in arterial pressure; these effects were prevented by phentolamine. 6. The results point to a continuing effect of prostaglandin synthesis in maintaining blood flow to the kidney and adrenal gland independent of α-adrenoceptor activation in resting conscious rabbits. An important modulating effect of prostaglandins on sympathetic vascular tone in the spleen is suggested.

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