Department of Biochemistry, Center of Biological Sciences, Universidade Federal de Santa Catarina, Campus Universitário, Florianópolis, Brazil.
J Pharm Pharmacol. 2022 Jan 5;74(1):13-21. doi: 10.1093/jpp/rgab128.
This study investigated the involvement of heme oxygenase-1 (HO-1) in the antidepressant-like effects of ursolic acid (UA), a plant-derived compound with neuroprotective and antidepressant-like properties.
Mice received intracerebroventricular injections of zinc protoporphyrin IX (ZnPP) or cobalt protoporphyrin IX (CoPP) to inhibit or induce HO-1, respectively, together with effective (0.1 mg/kg, p.o.) or sub-effective (0.01 mg/kg, p.o.) doses of UA or fluoxetine (10 mg/kg, p.o.). Immobility time was assessed using the tail suspension test (TST) and the ambulatory behaviour with the open field test. HO-1 immunocontent was evaluated in mice hippocampus and prefrontal cortex.
ZnPP prevented the anti-immobility effects of UA and fluoxetine. Combined treatment with a sub-effective dose of CoPP and UA synergistically exerted antidepressant-like effects in the TST. Acute administration of UA or CoPP, but not fluoxetine, increased the HO-1 immunocontent in the hippocampus. None of the treatments altered the HO-1 immunocontent in the prefrontal cortex.
In conclusion, this work shows that increased hippocampal HO-1 content and activity mediate the antidepressant-like effect of UA in the TST.
本研究旨在探讨血红素加氧酶-1(HO-1)是否参与了熊果酸(UA)的抗抑郁作用,UA 是一种具有神经保护和抗抑郁作用的植物衍生化合物。
通过向小鼠脑室内注射锌原卟啉 IX(ZnPP)或钴原卟啉 IX(CoPP),分别抑制或诱导 HO-1,同时给予有效(0.1mg/kg,po)或亚有效(0.01mg/kg,po)剂量的 UA 或氟西汀(10mg/kg,po)。使用悬尾试验(TST)评估不动时间,使用旷场试验评估活动行为。在小鼠海马体和前额叶皮层中评估 HO-1 免疫含量。
ZnPP 阻止了 UA 和氟西汀的抗不动作用。亚有效剂量的 CoPP 与 UA 联合治疗在 TST 中具有协同的抗抑郁作用。UA 或 CoPP 的急性给药可增加海马体中的 HO-1 免疫含量,但氟西汀则没有。这些治疗均未改变前额叶皮层中的 HO-1 免疫含量。
总之,本研究表明,增加海马体中的 HO-1 含量和活性介导了 UA 在 TST 中的抗抑郁作用。