Targeted delivery of pharmacological agents into rat dorsal root ganglion

被引:24
|
作者
Puljak, Livia [1 ]
Kojundzic, Sanja Lovric [1 ]
Hogan, Quinn H. [2 ]
Sapunar, Damir [1 ]
机构
[1] Univ Split, Sch Med, Dept Anat Histol & Embryol, Split 21000, Croatia
[2] Med Coll Wisconsin, Dept Anesthesiol, Milwaukee, WI 53226 USA
关键词
Rat; Dorsal root ganglion; Injections; Neuropathic pain; Pain models; PERIPHERAL-NERVE INJURY; PRIMARY SENSORY NEURONS; NEUROPATHIC PAIN; MECHANICAL HYPERALGESIA; CYCLIC-AMP; CELL BODY; MODEL; EXPRESSION; INFLAMMATION;
D O I
10.1016/j.jneumeth.2008.10.029
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We sought an optimal method for targeted delivery into dorsal root ganglia (DRGs) for experimental studies, in terms of precision of delivery and avoidance of behavioral disturbances. We examined three approaches for injection into rat DRGs: percutaneous injection without surgical exposure, injection after deep exposure, and injection following deep exposure and partial laminectomy. Coomassie blue and Fast Blue were injected into DRGs for validation. At necropsy, the spread of Coomassie blue and Fast Blue was investigated under stereomicroscope and fluorescent microscope, respectively. We found that percutaneous approach did not provide any successful DRG injections. Deep exposure prior to intraganglionic injection provided variable results, but intraganglionic injection after deep exposure plus partial laminectomy was successful in 100% of attempts, Our subsequent skeletal analysis showed that the anatomical location of DRG is not compatible with successful DRC injection without surgical exposure. Neither of the methods using surgical exposure caused behavioral disturbances. Based on these results we conclude that partial laminectomy offers the most precise method of injecting DRG and does not produce behavioral evidence of nerve damage. Intraganglionic injection after deep exposure alone is less predictable, while percutaneous approaches only allow injection in the peripheral nerve. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:397 / 402
页数:6
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