Barbe Mary F, Gomez-Amaya Sandra, Braverman Alan S, Brown Justin M, Lamarre Neil S, Massicotte Vicky S, Lewis Jennifer K S, Dachert Stephen R, Ruggieri Michael R
Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, Pennsylvania.
CAIF A1224, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania.
Neurourol Urodyn. 2017 Jan;36(1):91-97. doi: 10.1002/nau.22904. Epub 2015 Oct 9.
Complete spinal cord injury does not block perceptual responses or inferior solitary nucleus activation after genital self-stimulation, even though the vagus is not thought to innervate pelvic structures. We tested if vagus nerve endings sprout after bladder decentralization to innervate genitourinary structures in canines with decentralized bladders.
Four reinnervation surgeries were performed in female hounds: bilateral genitofemoral nerve transfer to pelvic nerve with vesicostomy (GNF-V) or without (GFN-NV); and left femoral nerve transfer (FNT-V and FNT-NV). After 8 months, retrograde dyes were injected into genitourinary structures. Three weeks later, at euthanasia, reinnervation was evaluated as increased detrusor pressure induced by functional electrical stimulation (FES). Controls included un-operated, sham-operated, and decentralized animals.
Increased detrusor pressure was seen in 8/12 GFNT-V, 4/5 GFNT-NV, 5/5 FNT-V, and 4/5 FNT-NV animals after FES, but not decentralized controls. Lumbar cord segments contained cells labeled from the bladder in all nerve transfer animals with FES-induced increased detrusor pressure. Nodose ganglia cells labeled from the bladder were observed in 5/7 nerve transfer animals (1/2 GNT-NV; 4/5 FNT-V), and from the clitoris were in 6/7 nerve transfer animals (2/2 GFNT-NV; 4/5 FNT-V). Dorsal motor nucleus vagus cells labeled from the bladder were observed in 3/5 nerve transfer animals (1/2 GFNT-NV; 2/3 FNT-V), and from the clitoris in 4/5 nerve transfer animals (1/2 GFNT-NV; 3/3 FNT-V). Controls lacked this labeling.
Evidence of vagal nerve sprouting to the bladder and clitoris was observed in canines with lower motoneuron lesioned bladders. Neurourol. Urodynam. 36:91-97, 2017. © 2015 Wiley Periodicals, Inc.
完全性脊髓损伤并不会阻断生殖器自我刺激后的知觉反应或孤束核下部激活,即便迷走神经被认为并不支配盆腔结构。我们测试了在膀胱去传入神经支配后,迷走神经末梢是否会在犬类动物中萌出以支配去传入神经支配的膀胱的泌尿生殖结构。
对雌性猎犬进行了四项再支配手术:双侧生殖股神经转移至带膀胱造瘘术的盆腔神经(GNF-V)或不带膀胱造瘘术(GFN-NV);以及左侧股神经转移(FNT-V和FNT-NV)。8个月后,将逆行染料注入泌尿生殖结构。三周后,在安乐死时,通过功能性电刺激(FES)诱导的逼尿肌压力增加来评估再支配情况。对照组包括未手术、假手术和去传入神经支配的动物。
FES后,在8/12只GNF-V、4/5只GFN-NV、5/5只FNT-V和4/5只FNT-NV动物中观察到逼尿肌压力增加,但去传入神经支配的对照组未出现。在所有因FES诱导逼尿肌压力增加的神经转移动物中,腰髓节段含有从膀胱标记的细胞。在5/7只神经转移动物中观察到从膀胱标记的结状神经节细胞(1/2只GNT-NV;4/5只FNT-V),从阴蒂标记的在6/7只神经转移动物中(2/2只GFNT-NV;4/5只FNT-V)。在3/5只神经转移动物中观察到从膀胱标记的迷走神经背运动核细胞(1/2只GFNT-NV;2/3只FNT-V),从阴蒂标记的在4/5只神经转移动物中(1/2只GFNT-NV;3/3只FNT-V)。对照组缺乏这种标记。
在患有下运动神经元损伤膀胱的犬类动物中观察到迷走神经向膀胱和阴蒂萌出的证据。《神经泌尿学与尿动力学》36:91 - 97,2017年。© 2015威利期刊公司。