Laboratory for Biomaterials and Drug Delivery, Department of Anesthesiology, Division of Critical Care Medicine, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Biomaterials. 2012 May;33(13):3586-93. doi: 10.1016/j.biomaterials.2012.01.043. Epub 2012 Feb 16.
Concerns over neurotoxicity have impeded the development of sustained release formulations providing prolonged duration local anesthesia (PDLA) from a single injection, for which there is an urgent clinical need. Here, we have used toxicogenomics to investigate whether nerve injury occurred during week-long continuous sciatic nerve blockade by microspheres containing bupivacaine, tetrodotoxin, and dexamethasone (TBD). Animals treated with amitriptyline solution (our positive control for local anesthetic-associated nerve injury) developed irreversible nerve blockade, had severely abnormal nerve histology, and the expression of hundreds of genes was altered in the dorsal root ganglia at 4 and 7 days after injection. In marked contrast, TBD-treated nerves reverted to normal function, were normal histologically and there were changes in the expression of a small number of genes. Toxicogenomic studies have great potential in delineating patterns of gene expression associated with specific patterns of tissue injury (e.g. amitriptyline neurotoxicity), and in identifying related changes in gene expression upon exposure to a drug, biomaterial, or drug delivery system.
人们对于神经毒性的担忧阻碍了长效局部麻醉(PDLA)的持续释放制剂的发展,这种制剂只需单次注射即可提供长时间的局部麻醉,目前临床上对此有迫切需求。在这里,我们使用毒理学基因组学来研究含有布比卡因、河豚毒素和地塞米松的微球在长达一周的连续坐骨神经阻滞过程中是否会造成神经损伤(TBD)。用阿米替林溶液(我们用于局部麻醉相关神经损伤的阳性对照)治疗的动物出现不可逆的神经阻滞,神经组织学严重异常,并且在注射后 4 天和 7 天,背根神经节中数百个基因的表达发生改变。相比之下,TBD 治疗的神经恢复正常功能,组织学正常,只有少数基因的表达发生变化。毒理学基因组学研究在描绘与特定组织损伤模式(例如阿米替林神经毒性)相关的基因表达模式方面具有巨大潜力,并可在暴露于药物、生物材料或药物输送系统时识别相关的基因表达变化。