Graniel-Amador Mayra Alejandra, Torres-Rodríguez Héctor Fabian, Martínez-Mendoza Ruth Elena, Vargas-Muñoz Virginia Margarita, Acosta-González Rosa Issel, Castañeda-Corral Gabriela, Muñoz-Islas Enriqueta, Jiménez-Andrade Juan Miguel
Laboratorio de Farmacología, Unidad Académica Multidisciplinaria Reynosa-Aztlán, UAT, Reynosa, Tamaulipas, México.
Facultad de Medicina, Universidad Autónoma del Estado de Morelos, Cuernavaca, Morelos, México.
Biometals. 2022 Oct;35(5):1033-1042. doi: 10.1007/s10534-022-00421-5. Epub 2022 Jul 18.
Type-1 diabetes mellitus (T1DM) is a chronic condition characterized by long-term hyperglycemia that results in several complications such as painful peripheral neuropathy, bone deterioration, and increased risk of bone fractures. Lithium, a first-line therapy for bipolar disorder, has become an attractive agent for attenuating peripheral neuropathy and menopause-induced bone loss. Therefore, our aim was to determine the effect of chronic lithium treatment on mechanical hypersensitivity and trabecular bone loss induced by T1DM in mice. T1DM was induced in male C57BL/6J mice by intraperitoneal injection of streptozotocin (STZ, 50 mg/kg/day, for 5 consecutive days). 12 weeks after T1DM-induction, mice received a daily intraperitoneal injection of vehicle, 30 or 60 mg/kg lithium (as LiCl) for 6 weeks. Throughout the treatment period, blood glucose levels and mechanical sensitivity were evaluated every 2 weeks. After lithium treatment, the femur and L5 vertebra were harvested for microcomputed tomography (microCT) analysis. T1DM mice showed significant hyperglycemia, mechanical hypersensitivity, and significant trabecular bone loss as compared with the control group. Chronic lithium treatment did not revert the hindpaw mechanical hypersensitivity nor hyperglycemia associated to T1DM induced by STZ. In contrast, microCT analysis revealed that lithium reverted, in a dose-dependent manner, the loss of trabecular bone associated to T1DM induced by STZ at both the distal femur and L5 vertebra. Lithium treatment by itself did not affect any trabecular bone parameter in non-diabetic mice.
1型糖尿病(T1DM)是一种慢性病,其特征为长期高血糖,会导致多种并发症,如疼痛性周围神经病变、骨质退化以及骨折风险增加。锂盐作为双相情感障碍的一线治疗药物,已成为减轻周围神经病变和绝经后骨质流失的一种有吸引力的药物。因此,我们的目的是确定慢性锂盐治疗对T1DM诱导的小鼠机械性超敏反应和小梁骨丢失的影响。通过腹腔注射链脲佐菌素(STZ,50mg/kg/天,连续5天)在雄性C57BL/6J小鼠中诱导T1DM。在诱导T1DM 12周后,小鼠每天接受腹腔注射溶剂、30或60mg/kg锂盐(以LiCl形式),持续6周。在整个治疗期间,每2周评估一次血糖水平和机械敏感性。锂盐治疗后,采集股骨和L5椎体进行显微计算机断层扫描(microCT)分析。与对照组相比,T1DM小鼠表现出显著的高血糖、机械性超敏反应和显著的小梁骨丢失。慢性锂盐治疗并未恢复由STZ诱导的T1DM相关的后爪机械性超敏反应或高血糖。相反,microCT分析显示,锂盐以剂量依赖性方式逆转了由STZ诱导的T1DM在股骨远端和L5椎体处的小梁骨丢失。锂盐治疗本身对非糖尿病小鼠的任何小梁骨参数均无影响。