Lee S L, Pevec W C, Carlsen R C
Department of Surgery, University of California, Davis Health System, Sacramento, CA 95817, USA.
J Vasc Surg. 2001 Dec;34(6):1096-102. doi: 10.1067/mva.2001.117889.
The administration of angiogenic growth factors and the transfer of well-vascularized tissues have been shown to induce development of new blood vessels in ischemic muscle. The functional significance of these new vessels is unknown. The hypothesis of this study is that the transfer of vascularized muscle and the local infusion of basic fibroblast growth factor (bFGF) synergistically improve contractile function of ischemic skeletal muscle.
Twenty-six rabbits were divided into four groups. An ischemic hindlimb was created in each by ligating the right common iliac artery. The flap + bFGF group (n = 6) had transposition of a contralateral rectus muscle flap onto the thigh. Additionally, bFGF (3 ng/h) was continuously infused at the flap-thigh interface. In the flap group (n = 6), a similar muscle flap was created, but carrier solution was infused at the interface. In the bFGF group (n = 6), no muscle flap was created; instead, bFGF (3 ng/h) was infused into the external iliac artery of the ischemic limb. In the control group (n = 8), carrier solution was infused into the external iliac artery (no flap, no bFGF). After 1 week, the soleus muscle was isolated and stimulated. Maximum twitch tension, the fatigue index (force of contraction after 2 minutes of continuous stimulation/initial force of contraction), maximum recovery, and the number of limbs recovered (ie, limbs that achieve a force of contraction during the recovery period of > 75% of the force of the initial contraction at the start of continuous stimulation) were recorded. Blood vessel density (number of vessels per ***) was determined by immunostaining the soleus muscle with anti-alpha-actin antibody.
All values were indexed to the contralateral normal limb. The flap + bFGF group showed significant improvement versus the control group in maximum twitch tension (1.07 +/- 0.13 vs 0.63 +/- 0.12, P < .05), maximum recovery (0.94 +/- 0.05 vs 0.58 +/- 0.05, P < .05), and the number of limbs recovered (5/5 vs 0/6, P < .05). This improved function correlated with increased vessel density (flap + bFGF group, 1.44 +/- 0.11 vs control group, 0.72 +/- 0.01, P < .05).
Reperfusion of an ischemic limb with a well-vascularized muscle flap and local bFGF infusion promoted increased blood vessel density in distal ischemic muscle. This increased vascularity was associated with restoration of otherwise impaired muscle function. Improved function occurred rapidly (1 week). A transposed muscle flap provided a functional blood supply to the site of maximum ischemia; this could be used to salvage otherwise nonreconstructible ischemic limbs.
血管生成生长因子的给药以及血运丰富组织的移植已被证明可诱导缺血肌肉中新生血管的形成。这些新血管的功能意义尚不清楚。本研究的假设是,血运丰富肌肉的移植与碱性成纤维细胞生长因子(bFGF)的局部输注协同改善缺血骨骼肌的收缩功能。
26只兔子分为四组。通过结扎右髂总动脉在每只兔子身上制造一只缺血后肢。皮瓣+bFGF组(n=6)将对侧直肌皮瓣转移至大腿。此外,在皮瓣-大腿界面持续输注bFGF(3 ng/h)。皮瓣组(n=6)制作了类似的肌肉皮瓣,但在界面处输注载体溶液。bFGF组(n=6)未制作肌肉皮瓣;相反,将bFGF(3 ng/h)注入缺血肢体的髂外动脉。对照组(n=8)将载体溶液注入髂外动脉(无皮瓣,无bFGF)。1周后,分离并刺激比目鱼肌。记录最大抽搐张力、疲劳指数(持续刺激2分钟后的收缩力/初始收缩力)、最大恢复力以及恢复肢体的数量(即,在恢复期收缩力达到持续刺激开始时初始收缩力的>75%的肢体)。通过用抗α-肌动蛋白抗体对比目鱼肌进行免疫染色来确定血管密度(每***血管数量)。
所有数值均以对侧正常肢体为参照。皮瓣+bFGF组与对照组相比,在最大抽搐张力(1.07±0.13对0.63±0.12,P<.05)、最大恢复力(0.94±0.05对0.58±0.05,P<.05)和恢复肢体数量(5/5对0/6,P<.05)方面有显著改善。这种功能改善与血管密度增加相关(皮瓣+bFGF组,1.44±0.11对对照组,0.72±0.01,P<.05)。
用血运丰富的肌肉皮瓣和局部bFGF输注对缺血肢体进行再灌注可促进远端缺血肌肉中血管密度增加。这种血管增多与原本受损的肌肉功能恢复相关。功能改善迅速(1周)。转移的肌肉皮瓣为最大缺血部位提供了功能性血供;这可用于挽救原本无法重建的缺血肢体。