2nd Department of Anesthesia, Nagano Red Cross Hospital, Wakasato, Nagano, Nagano, Japan.
Brain Res Bull. 2012 Dec 1;89(5-6):223-30. doi: 10.1016/j.brainresbull.2012.08.006. Epub 2012 Sep 7.
We have previously reported that halothane anesthesia increases extracellular concentrations of dopamine (DA) metabolites in rat striatum using in vivo microdialysis techniques. Aging induces many changes in the brain, including neurotransmission. However, the relationship between aging and changes in neurotransmitter release during inhalational anesthesia has not been fully investigated. The aim of the present investigation was to evaluate the effect of sevoflurane on methamphetamine (MAPT)-induced DA release and metabolism in young and middle-aged rats. Male Sprague-Dawley rats were implanted with a microdialysis probe into the right striatum. The probe was perfused with a modified Ringer's solution and 40μl of dialysate was directly injected to an HPLC every 20min. Rats were administered saline, the same volume of 2mgkg(-1) MAPT intraperitoneally, or 5μM MAPT locally perfused. After treatments, the rats were anesthetized with 1% or 3% sevoflurane for 1h. Sevoflurane anesthesia significantly increased the extracellular concentration of DA only in middle-aged rats (52-weeks-old). In young rats (8-weeks-old), sevoflurane significantly enhanced MAPT-induced DA when administered both intraperitoneally and perfused locally, whereas no significant additive interaction was found in middle-aged rats. These results suggest that aging changes DA release and metabolism in rat brains primarily by decreasing the DA transporter.
我们之前曾报道过,使用活体微透析技术,氟烷麻醉会增加大鼠纹状体细胞外多巴胺(DA)代谢物的浓度。衰老是大脑发生的许多变化之一,包括神经递质的变化。然而,吸入麻醉期间神经递质释放的变化与衰老之间的关系尚未得到充分研究。本研究旨在评估七氟醚对年轻和中年大鼠中 methamphetamine(MAPT)诱导的 DA 释放和代谢的影响。雄性 Sprague-Dawley 大鼠将微透析探针植入右侧纹状体。探针用改良的 Ringer 溶液灌注,每隔 20 分钟直接将 40μl 透析液注入 HPLC。大鼠接受生理盐水、相同体积的 2mgkg(-1)MAPT 腹腔内注射或 5μM MAPT 局部灌注。治疗后,大鼠用 1%或 3%七氟醚麻醉 1 小时。氟烷麻醉仅在中年大鼠(52 周龄)中显著增加细胞外 DA 浓度。在年轻大鼠(8 周龄)中,七氟醚显著增强了 MAPT 诱导的 DA,无论是腹腔内给药还是局部灌注给药,但在中年大鼠中未发现显著的附加相互作用。这些结果表明,衰老主要通过减少多巴胺转运体来改变大鼠大脑中的 DA 释放和代谢。