The ameliorating effect of dantrolene on the morphology of urinary bladder in spinal cord injured rats

被引:10
作者
Torres, Bruno [1 ]
Serakides, Rogeria [1 ]
Caldeira, Fatima [1 ]
Gomes, Mardelene [1 ]
Melo, Eliane [1 ]
机构
[1] Univ Fed Minas Gerais, Dept Vet Med & Surg, Sch Vet, Belo Horizonte, MG, Brazil
关键词
Dantrolene; Spinal cord injury; Urinary bladder injury; Rat; EXTERNAL URETHRAL SPHINCTER; NEURONAL CELL-DEATH; IN-VITRO; MALIGNANT HYPERTHERMIA; PROMOTE RECOVERY; TRAUMATIC INJURY; CONTUSION INJURY; THERAPEUTIC-USE; APOPTOSIS; SODIUM;
D O I
10.1016/j.prp.2011.10.004
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
In animal models of spinal cord injury (SCI), the urinary bladder can undergo significant structural and physiological alterations. Dantrolene has been shown to be neuroprotective by reducing neuronal apoptosis after SCI. Furthermore, in addition to its anti-inflammatory and antioxidant properties, it appears to have a beneficial action on voiding, once this drug acts on the external urethral sphincter relaxation. In the present study, we investigated the effects of dantrolene on urinary bladder injury that follows experimental SCI. Forty-six male Wistar rats were laminectomized at T13, and a compressive trauma was performed to induce SCI. After euthanasia, the urinary bladder was removed for gross and histological evaluation. Traumatized animals showed urinary retention with severe hemorrhagic cystitis. Injured animals treated with dantrolene had less bladder hemorrhage and inflammatory infiltrate than those treated with placebo (p < 0.05). Our results demonstrate that dantrolene may protect against urinary bladder lesions that follow SCI. Treating spinal cord-injured patients with this agent may be a promising additional therapeutic strategy to alleviate the accompanying inflammatory process. The results of the current study show that dantrolene has protective effects on spinal cord contusion-induced urinary bladder injury. The impaired integrity of bladder morphology was ameliorated by dantrolene treatment. (C) 2011 Elsevier GmbH. All rights reserved.
引用
收藏
页码:775 / 779
页数:5
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