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用于保留神经手术操作的亚甲蓝染色:一种动物模型。

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

作者信息

Seif Christoph, Martínez Portillo Francisco J, Osmonov Daniar K, Böhler Georg, van der Horst Christof, Leissner Joachim, Hohenfellner Rudolf, Juenemann Klaus P, Braun Peter M

机构信息

Department of Urology, University Hospital Kiel, Kiel, Germany.

出版信息

Urology. 2004 Jun;63(6):1205-8. doi: 10.1016/j.urology.2003.12.020.

Abstract

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.

摘要

目的

评估亚甲蓝纤维染色作为一种在动物模型中识别神经纤维的方法,因为手术后器官功能的维持取决于术中对相关神经纤维的准确识别。

方法

在六只小型猪双侧S3植入布林德利电极用于骶前根刺激。作为对照,通过尿动力学记录刺激诱发的逼尿肌收缩。在双侧暴露输尿管膀胱连接处后,将2:8的亚甲蓝溶液应用于右侧;左侧不做处理。在输尿管膀胱连接处近端4厘米范围内,从周围组织双侧游离输尿管。右侧亚甲蓝染色的神经纤维得以保留;左侧神经未作特别处理。再次通过尿动力学监测双侧骶前根刺激诱发的逼尿肌收缩。然后,故意切断右侧已识别的神经纤维,并在刺激下再次记录逼尿肌压力。最后,对分离的神经结构进行组织学评估。

结果

输尿管分离前左侧单侧刺激后的参考膀胱压力显示平均逼尿肌压力(Pdet)为19厘米水柱。右侧的Pdet为18厘米水柱。双侧处理后,左侧刺激后记录的平均Pdet为3厘米水柱,右侧刺激后为17厘米水柱。当右侧染色的神经纤维被切断时,无法诱发膀胱收缩。染色和分离结构的组织形态学显示结缔组织中有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且困难的任务。我们动物模型的结果表明,用亚甲蓝对自主神经纤维进行活体染色是一种简单可靠的识别方法。

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