LaNCE, Department Neuroscience, University of the Basque Country (UPV/EHU), Leioa, Bizkaia, Spain.
International Experimental Central Nervous System Injury & Repair (IECNSIR), Department of Surgical Sciences, Anesthesiology & Intensive Care Medicine, Uppsala University Hospital, Uppsala University, Uppsala, Sweden.
Adv Neurobiol. 2023;32:317-352. doi: 10.1007/978-3-031-32997-5_8.
Military personnel are often exposed to hot environments either for combat operations or peacekeeping missions. Hot environment is a severe stressful situation leading to profound hyperthermia, fatigue and neurological impairments. To avoid stressful environment, some people frequently use methamphetamine (METH) or other psychostimulants to feel comfortable under adverse situations. Our studies show that heat stress alone induces breakdown of the blood-brain barrier (BBB) and edema formation associated with reduced cerebral blood flow (CBF). On the other hand, METH alone induces hyperthermia and neurotoxicity. These effects of METH are exacerbated at high ambient temperatures as seen with greater breakdown of the BBB and brain pathology. Thus, a combination of METH use at hot environment may further enhance the brain damage-associated behavioral dysfunctions. METH is well known to induce severe oxidative stress leading to brain pathology. In this investigation, METH intoxication at hot environment was examined on brain pathology and to explore suitable strategies to induce neuroprotection. Accordingly, TiO-nanowired delivery of H-290/51 (150 mg/kg, i.p.), a potent chain-breaking antioxidant in combination with mesenchymal stem cells (MSCs), is investigated in attenuating METH-induced brain damage at hot environment in model experiments. Our results show that nanodelivery of H-290/51 with MSCs significantly enhanced CBF and reduced BBB breakdown, edema formation and brain pathology following METH exposure at hot environment. These observations are the first to point out that METH exacerbated brain pathology at hot environment probably due to enhanced oxidative stress, and MSCs attenuate these adverse effects, not reported earlier.
军人在作战或维和任务中经常暴露在炎热的环境中。炎热的环境是一种严重的应激情况,会导致严重的体温过高、疲劳和神经损伤。为了避免这种应激环境,一些人经常使用冰毒(METH)或其他兴奋剂来在不利情况下感到舒适。我们的研究表明,单独的热应激会导致血脑屏障(BBB)破裂和脑水肿形成,伴随着脑血流(CBF)减少。另一方面,METH 单独使用会导致体温过高和神经毒性。在高温环境下,METH 的这些作用会加剧,表现为 BBB 破裂和脑病理学加重。因此,在炎热环境下同时使用 METH 可能会进一步增强与大脑损伤相关的行为功能障碍。众所周知,METH 会引起严重的氧化应激,导致脑病理学。在这项研究中,研究了高温环境下 METH 中毒对脑病理学的影响,并探讨了诱导神经保护的合适策略。因此,在模型实验中,研究了 TiO-纳米载体传递 H-290/51(150mg/kg,腹腔注射)与间充质干细胞(MSCs)联合使用,以减轻高温环境下 METH 诱导的脑损伤。我们的研究结果表明,在高温环境下暴露于 METH 后,H-290/51 与 MSCs 的纳米传递显著增强了 CBF,减少了 BBB 破裂、脑水肿形成和脑病理学。这些观察结果首次指出,METH 在高温环境下加剧了脑病理学,可能是由于氧化应激增强,而 MSCs 减轻了这些以前未报道过的不良反应。