Abstract:Objective To investigate the autophagy of Cajal mesenchymal cells in the colon Cajal in rats with slow transit constipation, and qualitatively analyze the calcium ion level. Methods Forty healthy Wistar male rats were divided into control group (n=20, normal rats) and model group (n=20, model rats) by random number table. Compound phenylethylpiperidine was used for preparation on STC rat model, grain number, every grain of waste quality, body quality of rats, the first grain of black were recorded to judge the model successfully established or not. Colon ICCs of rats in two groups were detected bydetection of immunofluorescence assay, and the concentration of calcium ions in ICCs was determined by immunofluorescence assay. Results The control group had good growth during the experiment, and one died in the model group. Daily waste grain number, average body quality after 30 days in model group were less than those in the control group(P < 0.01), the average grain of feces quality was higher than that in the control group (P < 0.05), and the first row of black time was obviously prolonged in the control group (P < 0.05). The rats colon tissue of ICCs in control group were intertwined to form the intensive and precision of the mesh structure, they had obvious cell branch. The number of ICCs in the intestinal tract of the model group was significantly reduced, and the ICCs was thin and the cell shape narrowed. Compared with the control group, the autophagy number of ICCs in the model group increased and showed the apparent autophagy death. In the control group, ICCs were smooth and had multiple directional and irregular cell branches, and intercellular interaction was connected to the network structure. The number of fluorescence spots and fluorescence intensity in the ICCs of STC rats were significantly higher than those in the control group. Conclusion The number of ICCs in STC rats is reduced and autophagy is occurred. In the STC rat model, the free Ca2+ ions in the ICCs cells are elevated, and the increasing of Ca2+ ion may be the cause of the ICCs′ autophagy death.
田宇 毛於安▲. 慢传输型便秘大鼠结肠Cajal间质细胞自噬现象的发生及钙离子水平的定性分析[J]. 中国医药导报, 2018, 15(8): 20-23.
TIAN Yu MAO Yu′an▲. Autophagy of Cajal mesenchymal cells in the colon Cajal in rats with slow transit constipation and the qualitative analysis of calcium ion level. 中国医药导报, 2018, 15(8): 20-23.
[1] 高纺,盛红梅,张田宁,等.针刺不同穴方对便秘小鼠肠运动的影响[J].针刺研究,2017,42(1):62-66,75.
[2] 陈健海,仲婕,王凡,等.胃肠道Cajal间质细胞起搏功能的研究进展[J].中国病理生理杂志,2017,33(1):184-188.
[3] Tian H,Ge X,Nie Y,et al. Fecal microbiota transplantation in patients with slow-transit constipation:arandomized,clinical trial [J]. PLoS One,2017,12(2):e0 171 308.
[4] 程阔菊,罗云,彭雷,等.Cajal间质细胞在胃肠功能紊乱中的研究进展[J].胃肠病学和肝病学杂志,2015,24(6):749-750.
[5] Wang F,Tang J,Li P,et al. Chloroquine enhances the radiosensitivity of bladder cancer cells by inhibiting autophagy and activating apoptosis [J]. Cell Physiol Biochem,2017,45(1):54-66.
[6] 韦勇,杨四军.细胞自噬的调控与自噬程序性死亡的研究进展[J].国际免疫学杂志,2016,39(5):493-497.
[7] Cheng Z,Zhao K,Bi D. Simultaneous degeneration of myenteric plexuses andpelvic parasympathetic colonic nerve in slow transit constipation:a case report [J]. Medicine (Baltimore),2017,96(11):e6390.
[8] Raut PK,Choi DY,Kim SH,et al. Estrogen receptor signaling mediates leptin-induced growth of breast cancer cells via autophagy induction [J]. Oncotarget,2017,8(65):109 417-109 435.
[9] Zhu F,Xu S,Zhang Y,et al. Total glucosides of paeony promote intestinal motility in slow transit constipation rats through amelioration of interstitial cells of Cajal [J]. PLoS One,2016,11(8):e0 160 398.
[10] Liu K,Huang J,Xie M,et al. MIR34A regulates autophagy and apoptosis by targeting HMGB1 in the retinoblastoma cell [J]. Autophagy,2014,10(3):442-452.
[11] Booth LA,Tavallai S,Hamed HA,et al. The role of cell signalling in the crosstalk between autophagy and apoptosis [J]. Cell Signal,2014,26(3):549-555.
[12] Xie JM,Li B,Yu HP,et al. TIGAR has a dual role in cancer cell survival through regulating apoptosis and autophagy [J]. Cancer Res,2014,74(18):5127-5138.
[13] Goodall ML,Wang T,Martin KR,et al. Development of potent autophagy inhibitors that sensitize oncogenic BRAF V600E mutant melanoma tumor cells to vemurafenib [J]. Autophagy,2014,10(6):1120-1136.
[14] Meyers MJ,Anderson EJ,McNitt SA,et al. Evaluation of spiropiperidinehydantoins as a novel class of antimalarial agents [J]. Bioorg Med Chem,2015,23(16):5144-5150.
[15] Egbertson M,McGaughey GB,Pitzenberger SM,et al. Methyl-substitution of an iminohydantoinspiropiperidine β-secretase(BACE-1)inhibitor has a profound effect on its potency [J]. Bioorg Med Chem Lett,2015,25(21):4812-4819.
[16] Shin DH,Kim MW,Choi S,et al. Regulation of the pacemaker activity of colonic interstitial cells of Cajal by protease-activated receptors:involvement of hyperpolarization-activated cyclic nucleotide channels [J]. Pharmacology,2016,98(3-4):171-182.
[17] Kim HJ,Wie J,So I,et al. Menthol modulates pacemaker potentials through TRPA1 channels in cultured interstitial cells of Cajal from murine small intestine [J]. Cell Physiol Biochem,2016,38(5):1869-1882.
[18] Koleda P,Pilecki W. Nature of interstitial cells of Cajal of the upperurinary tract [J]. Adv Clin Exp Med,2014, 23(4):627-632.
[19] Kim HJ,Han T,Kim YT,et al. Magnolia officinalis bark extract induces depolarization of pacemaker potentials through M2 and M3 muscarinic receptors in cultured murine small intestine interstitial cells of Cajal [J]. Cell Physiol Biochem,2017,43(5):1790-1802.
[20] Kim HJ,Kim BJ. Naringenin inhibits pacemaking activity in interstitial cells of Cajal from murine small intestine [J]. Integr Med Res,2017,6(2):149-155.
[21] Radu BM,Banciu A,Banciu DD,et al. Calcium signalingin interstitial cells:focus on telocytes [J]. Int J MolSci,2017,18(2):113-115.