减轻辐射的氨基酸混合物对不同性别小鼠的影响

Mang Xiao, L. Hull, Alex Zizzo, Bin Lin, Min Zhai, Li Wang, Wanchang Cui
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引用次数: 0

摘要

迄今为止,美国食品和药物管理局(FDA)批准的用于治疗造血急性辐射综合征(H-ARS)的医疗对策寥寥无几。在本研究中,我们介绍了最新的研究成果,重点评估了一种新型辐射缓解剂--缓解氨基酸混合物(MAAM)。MAAM 由五种氨基酸组成,就像最近报道的用于缓解胃肠道(GI)-ARS 的氨基酸口服补液一样。将 CD2F1 雄性和雌性小鼠置于 60Co-γ 全身辐照 (TBI) 中,辐照剂量为 9.0 或 9.5 Gy。辐照后,小鼠口服 MAAM 或生理盐水对照品,从 TBI 24 小时后开始,每天一次,持续 14 天。照射后 30 天内监测小鼠的存活率和体重变化。利用第 30 天存活小鼠的样本分析了全血细胞计数(CBC)、骨髓干细胞和祖细胞存活率(克隆生成性)以及血清细胞因子抗体阵列。我们的数据显示,MAAM 治疗显著提高了辐照雄性 CD2F1 小鼠的存活率,在 9.0 Gy TBI 后,存活率从车辆对照组的 25% 提高到 MAAM 治疗组的 60%(p < 0.05)。在 9.0 Gy TBI 后,BM 菌落数从载体组的 41.8 ± 6.4 /104 个细胞显著增加到 MAAM 组的 78.5 ± 17.0 /104 个细胞。此外,MAAM 处理导致六种细胞因子/蛋白质水平下降[分化簇 40 (CD40)、白细胞介素 (IL)-17A、C-X-C 矩阵趋化因子 10 (CXCL10/CRG-2)、皮肤 T 细胞吸引趋化因子 (CTACK)、与载体组相比,小鼠血清中的其他五种细胞因子/蛋白质[IL-3Rβ、IL-5、瘦素、IL-6 和干细胞因子 (SCF)]水平在 9.0 Gy TBI。然而,在辐照后的 CD2F1 雌性小鼠中没有观察到类似的 MAAM 缓解效应。与辐照雄性小鼠相比,辐照雌性小鼠的血清细胞因子谱有所不同。总之,我们的数据表明,辐照后缓解性氨基酸联合疗法的有益效果可能取决于性别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of radiation mitigating amino acid mixture on mice of different sexes
To date, few FDA-approved medical countermeasures are available for addressing hematopoietic acute radiation syndrome (H-ARS). In this study, we present our latest research findings focusing on the evaluation of a novel radiation mitigator known as the mitigating amino acid mixture (MAAM). MAAM is composed of five amino acids as the recently reported amino acid-based oral rehydration solution for mitigating gastrointestinal (GI)-ARS. CD2F1 male and female mice were exposed to 60Co-γ total body irradiation (TBI) at 9.0 or 9.5 Gy. Following irradiation, mice were orally administered with MAAM or a saline vehicle control once daily for a duration of 14 days, commencing 24 h after TBI. Mouse survival and body weight change were monitored for 30 days after irradiation. Complete blood counts (CBCs), bone marrow (BM) stem and progenitor cell survival (clonogenicity), and a serum cytokine antibody array were analyzed using samples from day 30 surviving mice. Our data revealed that MAAM treatment significantly enhanced survival rates in irradiated male CD2F1 mice, and the survival rate increased from 25% in the vehicle control group to 60% in the MAAM-treated group (p < 0.05) after 9.0 Gy TBI. The number of BM colonies significantly increased from 41.8 ± 6.4 /104 cells (in the vehicle group) to 78.5 ± 17.0 /104 cells (in the MAAM group) following 9.0 Gy TBI. Furthermore, MAAM treatment led to a decrease in the levels of six cytokines/proteins [cluster of differentiation 40 (CD40), interleukin (IL)-17A, C–X–C motif chemokine 10 (CXCL10/CRG-2), cutaneous T cell-attracting chemokine (CTACK), macrophage inflammatory protein (MIP)-3β, and IL-1β] and an increase in the levels of five other cytokines/proteins [IL-3Rβ, IL-5, leptin, IL-6, and stem cell factor (SCF)] in mouse serum compared to the vehicle group after 9.0 Gy TBI. However, similar alleviating effects of MAAM were not observed in the irradiated CD2F1 female mice. The serum cytokine profile in the irradiated female mice was different compared to the irradiated male mice. In summary, our data suggest that the beneficial effects of the mitigative amino acid combination treatment after radiation exposure may depend on sex.
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