Yu X, Xu L, Zhang X D, Cui F Z
Biomaterials Laboratory, Department of Materials Science and Engineering, Tsinghua University, Beijing, China.
Urology. 2003 Oct;62(4):755-9. doi: 10.1016/s0090-4295(03)00486-2.
To determinate the effect of acute and chronic spinal cord injury (SCI) resulting from thoracic cord transection on the urinary bladder spinal neural pathway.
Seventy-six adult Sprague-Dawley rats were randomly divided into four groups, non-SCI (normal rats undergoing no surgical procedure except pseudorabies virus [PRV] injection), SCI(b) (SCI and PRV injected immediately after SCI), SCI(c) (SCI and PRV injected at 3 weeks after SCI), and SCI(d) (SCI and PRV injected at 3 months after SCI). Transcardiac perfusion fixation was done at appropriate survival periods after PRV injection into the bladder wall tissue. Sections of the dorsal root ganglion, spinal cord, and brain were processed for visualization of the virus by the streptavidin-peroxidase immunohistochemical procedure.
The bladder weight of the non-SCI, SCI(b), SCI(c), SCI(d) rats was 144 +/- 9 mg, 142 +/- 8 mg, 486 +/- 51 mg, and 656 +/- 69 mg, respectively. The time-ordered flow charts of PRV tracing were similar in the non-SCI and SCI rats. The cross-sectional area of the labeled dorsal root ganglion cell profiles increased significantly after SCI (P <0.001): 593 +/- 40 microm2, 588 +/- 39 microm2, 815 +/- 53 microm2, and 902 +/- 57 microm2 in the non-SCI, SCI(b), SCI(c), SCI(d) rats, respectively. The number of labeled cells in the dorsal horn in the L6 and S1 segments 3 days after PRV injection markedly increased in chronic SCI rats, as did the number of labeled motor neurons 4 days after injection.
Acute and chronic SCI have no effect on the process of virus transneuronal transport below the level of the lesion. Subsequent to chronic SCI, reorganization of the micturition reflex pathways may occur.
确定胸段脊髓横断所致急性和慢性脊髓损伤(SCI)对膀胱脊髓神经通路的影响。
76只成年Sprague-Dawley大鼠随机分为四组,即非SCI组(正常大鼠,除注射伪狂犬病病毒[PRV]外未接受任何手术)、SCI(b)组(SCI后立即注射PRV)、SCI(c)组(SCI后3周注射PRV)和SCI(d)组(SCI后3个月注射PRV)。将PRV注入膀胱壁组织后,在适当的存活期进行经心灌注固定。对背根神经节、脊髓和脑切片进行处理,采用链霉亲和素-过氧化物酶免疫组织化学方法观察病毒。
非SCI组、SCI(b)组、SCI(c)组、SCI(d)组大鼠的膀胱重量分别为144±9mg、142±8mg、486±51mg和656±69mg。PRV示踪的时间顺序流程图在非SCI组和SCI组大鼠中相似。SCI后标记的背根神经节细胞轮廓的横截面积显著增加(P<0.001):非SCI组、SCI(b)组、SCI(c)组、SCI(d)组大鼠分别为593±40μm2、588±39μm2、815±53μm2和902±57μm2。PRV注射3天后,慢性SCI大鼠L6和S1节段背角标记细胞数量明显增加,注射4天后标记运动神经元数量也明显增加。
急性和慢性SCI对损伤水平以下的病毒跨神经元运输过程无影响。慢性SCI后,排尿反射通路可能会发生重组。