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Methylene blue staining for nerve-sparing operative procedures: an animal model.

机译:亚甲基蓝染色用于保留神经的手术程序:一种动物模型。

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OBJECTIVES: To evaluate methylene blue fiber staining as a method of nerve fiber identification in an animal model, because the maintenance of organ function after surgery depends on exact intraoperative identification of the relevant nerve fibers. METHODS: Brindley electrodes were implanted bilaterally at S3 for sacral anterior root stimulation in six minipigs. For reference, stimulation-induced detrusor contractions were recorded urodynamically. After exposure of the ureterovesical junction on both sides, a 2:8 methylene blue solution was applied to the right side; the left side remained untreated. Bilateral dissection of the ureter from the surrounding tissue for a distance of 4 cm proximal to the ureterovesical junction was performed. The methylene blue-stained nerve fibers on the right side were spared; no particular attention was paid to the nerves on the left. Again, sacral anterior root stimulation-induced detrusor contractions were monitored urodynamically on both sides. Then, the identified nerve fibers on the right were cut intentionally, and the detrusor pressure was recorded again under stimulation. Finally, the dissected nerve structures were evaluated histologically. RESULTS: The reference bladder pressures after unilateral stimulation on the left side before ureter dissection showed a mean detrusor pressure (Pdet) of 19 cm H2O. On the right side, the Pdet was 18 cm H2O. After preparation on both sides, a mean Pdet of 3 cm H2O was recorded after left side stimulation, and a Pdet of 17 cm H2O after right side stimulation. When the stained nerve fibers on the right side were cut, no bladder contractions could be induced. The histomorphology of the stained and dissected structures revealed multiple autonomous nerve fibers and small vessels in connective tissue. CONCLUSIONS: The identification of minute nerve bundles is a tedious and difficult task. The results from our animal model demonstrated that supravital staining of autonomous nerve fibers with methylene blue is a simple and reliable method of identification.
机译:目的:评价亚甲基蓝纤维染色作为动物模型中神经纤维鉴定的一种方法,因为手术后器官功能的维持取决于相关神经纤维的确切术中鉴定。方法:在S3两侧植入Brindley电极,对6只小型猪的前根进行刺激。作为参考,尿动力学记录刺激诱发的逼尿肌收缩。输尿管膀胱交界处的两侧都暴露后,将2:8的亚甲蓝溶液施加到右侧。左侧未治疗。将输尿管从周围组织进行双侧解剖,距离输尿管膀胱交界处近4 cm。右侧保留了亚甲蓝染色的神经纤维。没有特别注意左侧的神经。再次,在尿路动力学两侧监测前根刺激引起的逼尿肌收缩。然后,有意识地切断右侧识别出的神经纤维,并在刺激下再次记录逼尿肌压力。最后,对解剖的神经结构进行组织学评估。结果:在进行输尿管解剖之前,左侧单侧刺激后的参考膀胱压力显示出平均逼尿肌压力(Pdet)为19 cm H2O。在右侧,Pdet为18 cm H2O。两侧准备后,左侧刺激后记录的平均Pdet为3 cm H2O,右侧刺激后记录的平均Pdet为17 cm H2O。切掉右侧的染色神经纤维时,不会引起膀胱收缩。染色和解剖结构的组织形态学显示结缔组织中多条自主神经纤维和小血管。结论:识别微小神经束是一项繁琐而艰巨的任务。我们动物模型的结果表明,用亚甲基蓝对自主神经纤维进行表面染色是一种简单而可靠的识别方法。

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