Department of Toxicology, School of Public Health, Guangxi Medical University, No. 22, Shuang-yong Rd, Nanning, 530021, Guangxi, China.
Guangxi Colleges and Universities Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, Nanning, China.
Biol Trace Elem Res. 2021 Oct;199(10):3759-3771. doi: 10.1007/s12011-020-02516-x. Epub 2021 Jan 6.
Sodium p-aminosalicylic acid (PAS-Na) has been previously shown to protect the brain from manganese (Mn)-induced toxicity. However, the efficacy of PAS-Na in protecting other organs from Mn toxicity and the mechanisms associated with this protection have yet to be addressed. Therefore, here, we assessed pancreatic damage in response to Mn treatment and the efficacy of PAS-Na in limiting this effect, along with specific mechanisms that mediate PAS-Na's protection. Mn exposure led to increased blood Mn content in dose- and time-dependent manner. Furthermore, subchronic Mn exposure (20 mg/kg for 8 weeks) led to pancreatic damage in a dose-dependent manner. In addition, the elevated Mn levels increased iron and decreased zinc and magnesium content in the pancreas. These effects were noted even 8 weeks after Mn exposure cessation. Mn exposure also affected the levels of amylase, lipase, and inflammatory factors such as tumor necrosis factor (TNF-α) and interleukin-1 β (IL-1β). PAS-Na significantly inhibited the increase in Mn concentration in both blood and pancreas, restored Mn-induced pancreatic damage, reversed the Mn-induced alterations in metal levels, and restored amylase and lipase concentrations. Taken together, we conclude that in rats, PAS-Na shows pharmacological efficacy in protecting the pancreas from Mn-induced damage.
对氨基水杨酸钠(PAS-Na)先前已被证明可保护大脑免受锰(Mn)诱导的毒性。然而,PAS-Na 保护其他器官免受 Mn 毒性的功效以及与这种保护相关的机制尚未得到解决。因此,在这里,我们评估了 Mn 处理后胰腺损伤以及 PAS-Na 限制这种作用的功效,以及介导 PAS-Na 保护的特定机制。Mn 暴露以剂量和时间依赖的方式导致血液 Mn 含量增加。此外,亚慢性 Mn 暴露(20 mg/kg 持续 8 周)以剂量依赖性方式导致胰腺损伤。此外,升高的 Mn 水平增加了胰腺中的铁含量,降低了锌和镁含量。即使在 Mn 暴露停止 8 周后,也观察到了这些影响。Mn 暴露还影响了淀粉酶、脂肪酶和炎症因子(如肿瘤坏死因子(TNF-α)和白细胞介素-1β(IL-1β))的水平。PAS-Na 显著抑制了血液和胰腺中 Mn 浓度的增加,恢复了 Mn 诱导的胰腺损伤,逆转了 Mn 诱导的金属水平改变,并恢复了淀粉酶和脂肪酶浓度。综上所述,我们得出结论,在大鼠中,PAS-Na 显示出药理学功效,可保护胰腺免受 Mn 诱导的损伤。