Department of General Surgery, Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt.
Eur J Vasc Endovasc Surg. 2010 Jul;40(1):81-7. doi: 10.1016/j.ejvs.2010.02.014. Epub 2010 Mar 20.
This study aimed to compare arteriogenesis after femoral artery occlusion as influenced by exercise or arteriovenous shunt and follow changes in collateral transient receptor potential cation channel, subfamily V, member 4 (Trpv4).
A prospective, controlled study wherein rats were subjected to femoral artery ligation (FAL), or FAL+arteriovenous shunt. Collateral Trpv4 was determined 0.5 and 6h post exercise.
Rats were subjected to exercise for 15 min, twice daily. The number and diameter of collaterals were assessed after 7 days. Collateral Trpv4 expression was quantified by reverse transcription-polymerase chain reaction.
Collateral number and diameter per limb were significantly higher in the shunt group (number: 16.0+/-2.4 and diameter: 216.0+/-34 microm) compared to the ligature (number: 9.4+/-2 and diameter: 144+/-21 microm) and exercise groups (number: 9.9+/-2.5 and diameter: 151+/-15 microm). Trpv4 expression in collaterals harvested 0.5h post exercise was not significantly different from expression in shunted rats. It was significantly lower in collaterals harvested 6h post exercise (comparable to that in ligated rats).
Collateral formation was greater in the shunt group than in the exercise group. Exercise-induced Trpv4 up-regulation, not significantly different from that achieved with shunt, returned to control values when evaluated 6h post exercise. More frequent exercise to chronically increase fluid shear stress, as with a shunt model, may be required for sufficient arteriogenesis to compensate for peripheral occlusion.
本研究旨在比较股动脉闭塞后运动或动静脉分流对动脉生成的影响,并观察侧支瞬态受体电位阳离子通道亚家族 V 成员 4(TRPV4)的变化。
前瞻性对照研究,大鼠接受股动脉结扎(FAL)或 FAL+动静脉分流。运动后 0.5 和 6 小时测定侧支 TRPV4。
大鼠每天运动 15 分钟,2 次/d。7 天后评估侧支数量和直径。通过逆转录-聚合酶链反应定量测定侧支 TRPV4 表达。
与结扎组(数量:9.4±2 个,直径:144±21 µm)和运动组(数量:9.9±2.5 个,直径:151±15 µm)相比,分流组侧支数量和直径/肢体明显更高(数量:16.0±2.4 个,直径:216.0±34 µm)。运动后 0.5 小时采集的侧支中 TRPV4 的表达与分流大鼠的表达无显著差异。运动后 6 小时采集的侧支中 TRPV4 的表达明显降低(与结扎大鼠相当)。
分流组的侧支形成大于运动组。运动诱导的 TRPV4 上调与分流相似,但在运动后 6 小时评估时,其表达恢复至对照值。为了补偿外周闭塞,可能需要更频繁的运动来慢性增加流体切应力,就像分流模型一样。