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预处理对急性低压缺氧暴露大鼠血清PHD2/HIF-1α水平及脑组织损伤的影响

[Effect of pretreatment on serum level of PHD2/HIF-1α and brain tissue damage in rats during acute hypobaric hypoxia exposure].

作者信息

Li Xiao-Ya, Wu Chun-Hua, Yan Ying-Jie, Wang Deng-Hui, Wang Meng-Jie, Hou Zhong-Wei

机构信息

College of Acupuncture-Moxibustion and Tuina, Beijing University of CM, Beijing 100029, China.

出版信息

Zhongguo Zhen Jiu. 2022 Nov 12;42(11):1278-84. doi: 10.13703/j.0255-2930.20211201-k0004.

Abstract

OBJECTIVE

To observe the effect of ( stone plaste) pretreatment on serum level of prolyl hydroxylase domain 2 (PHD2) and hypoxia-inducible factor-1α (HIF-1α) in rats with acute hypobaric hypoxia induced-brain injury, and to explore the possible mechanism of on preventing brain injury at high altitude.

METHODS

Forty-five male SD rats were randomly divided into a blank group, a model group, a Biantie group, a medication group and a Biantie+inhibitor group, 9 rats in each group. The rats in the Biantie group the and the Biantie+inhibitor group were pretreated with at "Taiyuan" (LU 9), "Neiguan" (PC 6) and "Renying" (ST 9), 2 h each time, once a day; the rats in the medication group were treated with intragastric administration of rhodiola capsule solution (280 mg/kg) for 14 d; the rats in the Biantie+inhibitor group were intraperitoneally injected with the PHD inhibitor dimethyloxalyl glycine (DMOG) at a dose of 40 mg/kg 24 h before the establishment of the model. After the intervention, except for the blank group, the rats in the remaining 4 groups were placed in the oxygen chamber to simulate a high-altitude environment to establish the acute hypobaric hypoxia brain injury model. The arterial blood-gas analysis indexes [blood oxygen saturation (SaO), lactic acid (Lac), blood sodium (Na), blood potassium (K)] and brain water content were detected in each group; the histomorphology of cerebral cortex was observed by HE staining; the serum levels of PHD2 and HIF-1α as well as vascular endothelial growth factor (VEGF) were detected by ELISA; the VEGF protein expression in brain tissue was detected by Western blot; the VEGF mRNA expression in brain tissue was detected by real-time fluorescent quantitative PCR.

RESULTS

Compared with the blank group, the levels of SaO and Na in the model group were decreased (<0.05), while the levels of Lac and K as well as the water content of brain tissue were increased (<0.05). Compared with the model group, the level of SaO in the Biantie group and the medication group was increased (<0.05), while the levels of Lac, K and the water content of brain tissue were decreased (<0.05); the level of Na in the Biantie group was increased (<0.05). Compared with the Biantie group, the level of SaO in the Biantie+inhibitor group was decreased (<0.05), and the level of Lac and the water content of brain tissue were increased (<0.05). In the model group, the cortical tissue cells were loose and disordered, the cortical blood vessels were dilated, and the cells were obviously swollen; the anoxic injury in the Biantie group and the medication group was lighter, and the anoxic injury in the Biantie+inhibitor group was more obvious than that in the Biantie group. Compared with the blank group, the serum PHD2 content in the model group was decreased and the HIF-1α content was increased (<0.05), and the content of VEGF in serum and VEGF protein and mRNA expressions in brain were increased (<0.05). Compared with the model group, the content of PHD2 in serum in the Biantie group and the medication group was increased (<0.05), and the level of HIF-1α was decreased (<0.05), and the content of VEGF in serum as well as VEGF protein and mRNA expressions in brain were decreased (<0.05). Compared with the Biantie group, the serum PHD2 content in the Biantie+inhibitor group was decreased and HIF-1α level were increased (<0.05), and the content of VEGF in serum as well as VEGF mRNA expression in brain were increased (<0.05).

CONCLUSION

at "Taiyuan" (LU 9), "Neiguan" (PC 6) and "Renying" (ST 9) could regulate serum PHD2/HIF-1α to down-regulate VEGF expression, reduce brain edema and enhance anti-hypoxia ability, so as to achieve the purpose of preventing brain injury at high altitude.

摘要

目的

观察砭石预处理对急性低压缺氧性脑损伤大鼠血清脯氨酰羟化酶结构域2(PHD2)及缺氧诱导因子-1α(HIF-1α)水平的影响,探讨砭石预防高原脑损伤的可能机制。

方法

将45只雄性SD大鼠随机分为空白组、模型组、砭石组、药物组和砭石+抑制剂组,每组9只。砭石组和砭石+抑制剂组大鼠于“太渊”(LU 9)、“内关”(PC 6)、“人迎”(ST 9)穴进行砭石预处理,每次2 h,每日1次;药物组大鼠灌胃给予红景天胶囊溶液(280 mg/kg),连续14 d;砭石+抑制剂组大鼠在造模前24 h腹腔注射PHD抑制剂二甲基乙二醛甘氨酸(DMOG),剂量为40 mg/kg。干预后,除空白组外,其余4组大鼠置于氧舱模拟高原环境建立急性低压缺氧性脑损伤模型。检测各组动脉血气分析指标[血氧饱和度(SaO)、乳酸(Lac)、血钠(Na)、血钾(K)]及脑组织含水量;HE染色观察大脑皮质组织形态学;ELISA法检测血清PHD2、HIF-1α及血管内皮生长因子(VEGF)水平;Western blot法检测脑组织VEGF蛋白表达;实时荧光定量PCR法检测脑组织VEGF mRNA表达。

结果

与空白组比较,模型组SaO、Na水平降低(P<0.05),Lac、K水平及脑组织含水量升高(P<0.05)。与模型组比较,砭石组和药物组SaO水平升高(P<0.05),Lac、K水平及脑组织含水量降低(P<0.05);砭石组Na水平升高(P<0.05)。与砭石组比较,砭石+抑制剂组SaO水平降低(P<0.05),Lac水平及脑组织含水量升高(P<0.05)。模型组皮质组织细胞疏松、排列紊乱,皮质血管扩张,细胞明显肿胀;砭石组和药物组缺氧损伤较轻,砭石+抑制剂组缺氧损伤较砭石组明显。与空白组比较,模型组血清PHD2含量降低,HIF-1α含量升高(P<0.05),血清VEGF含量及脑组织VEGF蛋白、mRNA表达升高(P<0.05)。与模型组比较,砭石组和药物组血清PHD2含量升高(P<0.05),HIF-1α水平降低(P<0.05),血清VEGF含量及脑组织VEGF蛋白、mRNA表达降低(P<0.05)。与砭石组比较,砭石+抑制剂组血清PHD2含量降低,HIF-1α水平升高(P<0.05),血清VEGF含量及脑组织VEGF mRNA表达升高(P<0.05)。

结论

砭石于“太渊”(LU 9)、“内关”(PC

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