摘要
目的:小鼠弓状核损毁是否影响胃组织和血浆nesfatin-1水平。方法:新生健康昆明小白鼠。谷氨酸单钠(MSG)处理组小鼠出生后1、3、5、7、9d于颈部皮下注射MSG。取胃组织行RT-PCR、免疫印迹,检测nesfatin-1mRNA及蛋白质水平,分别断头取脑,冷冻切片观察弓状核损毁情况。结果:与生理盐水组小鼠相比,MSG组小鼠弓状核甲酚紫染色神经元明显减少,体质量明显增加;禁食48h后胃黏膜组织NUCB2mRNA及蛋白表达明显低于禁食前,血浆nesfatin-1水平明显低于禁食前;MSG组小鼠与生理盐水组小鼠比较,在禁食前后,胃黏膜组织NUCB2mRNA和蛋白表达水平无明显改变,血浆nesfatin-1水平无明显改变。结论:弓状核损毁并没有影响胃黏膜NUCB2/nesfatin-1的合成、分泌以及血浆nesfatin-1水平。
Objective: To determine whether the arcuate nucleus lesion affect on nesfatin-1 level of stomach tissue and plasma level. Methods : The mice were injected subcutaneously in the dorsal dermis area just below the interscapular region on d 1, 3, 5, 7, and 9 after birth, with 10/A of MSG, and control mice were treated with saline. At 12 weeks of age, before and after food deprivation, the mice were then anesthetized (pentobarbital sodium, 50 mg/kg ip), body mass were measured, orbital blood was taken, stomach tissues were removed for RT-PCR and Western blotting, and the brains were removed and stored in a 4O//oo paraformaldehyde solution for arcuate nucleus lesion verification. Results: Compared with the saline controls, MSG treatment significantly decreased Nissl staining of the arcuate nucleus, MSG treatment significantly increased body mass. NUCB2 mRNA and protein of stomach, and plasma nesfatin-1 level were significantly decreased in MSG treated mice and saline treated mice fasted for 48 h compared with their respective counterparts before fasting, while there were no significant difference of NUCB2 mRNA and protein of the stomach, and plasma nesfatin-1 level between MSG treated mice and saline treated mice before and after fasting. Conclusion : Fasting for 48 h may decrease NUCB2 mRNA and protein expression of the stomach, and plasma nesfatin-1 level in two groups. Arcuate nucleus lesion did not affect the synthesis and releasing of NUCB2/nesfatin-1 of gastric tissues and the plasma nesfatin-1 level.
出处
《解剖学杂志》
CAS
CSCD
北大核心
2013年第6期1057-1061,共5页
Chinese Journal of Anatomy
基金
山东省医药卫生科技发展计划(2011QZ002)
滨州医学院科技计划(BY2010KYQD03)