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The effects of Lycium barbarum and Salvia miltiorrhiza on the histomorphology and CRYAB mRNA of retinal pigment degeneration rats |
LIU Jiaqi1 WANG Ying1 JIANG Pengfei1 PAN Kun1 XU Jian1 PENG Jun2,3 PENG Qinghua1,2,3 |
1.College of Integrated Traditional Chinese and Western Medicine, Hu′nan University of Chinese Medicine, Hu′nan Province, Changsha 410208, China; 2.Department of Ophthalmology, the First Hospital of Hu′nan University of Chinese Medicine, Hu′nan Province, Changsha 410007, China;
3.Key Laboratory of Traditional Chinese Medicine for Prevention and Treatment of Eye, Ear, Nose and Throat Diseases in Hu′nan Province, Hu′nan Province, Changsha 410208, China |
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Abstract Objective To observe the effects of Lycium barbarum and Salvia miltiorrhiza on the morphology of retinal tissue and alpha B-crystalline (CRYAB) mRNA in rats with retinitis pigmentosa. Methods Twenty-four male and female retinitis pigmentosa RCS (rdy-/-, p-/-) rats were divided into a model group and a ginseng group according to random number table method, with 8 rats in each group, 4 males and 4 females. Another 8 RCS (rdy+/+, p+/+) rats, 4 males and 4 females, were blank group. Oral gavage was started 1 week after routine feeding, once a day. The blank group and the model group were given normal saline, and the ginseng group was given an equivalent dose of Lycium barbarum + Salvia miltiorrhiza. The rats were sacrificed for 30 days after continuous gavage. The morphological changes of the outer nuclear layer of the retina of each group were observed under light microscope. The expression of CRYAB mRNA in RCS rats was detected by qPCR. Results The results of HE staining showed that the retinal structure of each layer in the blank group was neatly arranged and regular in shape. The retinal structure of the model group was looser, with degeneration and atrophy, and the thickness of the outer nuclear layer was significantly thinner, the difference was highly statistically significant (P < 0.01). Compared with the blank group, the ginseng group had a disordered structure and thinner thickness, but it had increased thickness compared with the model group, and the difference was highly statistically significant (P < 0.01). The results of qPCR showed that the expression of CRYAB mRNA was observed in the retina of rats in the blank group. The expression of CRYAB mRNA in the retina of the model group was significantly decreased compared with the blank group (P < 0.01). The expression of CRYAB mRNA in the retina of the ginseng group was higher than that in the model group and the difference was highly statistically significant (P < 0.01). Conclusion RCS rats can well simulate the pathogenesis of human retinitis pigmentosa. The structure of the retina is disordered, the outer nuclear layer is thinned, the expression of CRYAB mRNA in the retina is inhibited, and Lycium barbarum + Salvia miltiorrhiza can induce the expression of CRYAB mRNA in the retina. It has a certain protective effect on the retina of retinitis pigmentosa RCS rats.
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[1] Jones BW,Pfeiffer RL,Ferrell WD,et al. Retinal remodeling in human retinitis pigmentosa [J]. Exp Eye Res,2016, 150(2):149-165.
[2] Pawlyk BS,Bulgakov OV,Sun X,et al. Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa [J]. Gene Ther,2016, 23(2):196.
[3] 董玉萍,王磊峰,董秋艳,等.视网膜色素变性的流行病学调查[J].武警医学,2015,26(9):950-952.
[4] Marchena M,Villarejo-Zori B,Zaldivar-Diez J,et al. Small molecules targeting glycogen synthase kinase 3 as potential drug candidates for the treatment of retinitis pigmentosa [J]. J Enzyme Inhib Med Chem,2017,32(1):522-526.
[5] 刘家琦,李凤鸣.实用眼科学[M].3版.北京:人民卫生出版社,2015:451-453.
[6] 邓新国,张清炯,胡世兴,等.川芎嗪对视网膜色素变性rd小鼠的干预作用及其抗凋亡作用机制研究[J].中国中医眼科杂志,2006,16(3):148-152.
[7] Gangalum RK,Bhat AM,Kohan SA,et al. Inhibition of the Expression of the Small Heat Shock Protein alphaB-Crystallin Inhibits Exosome Secretion in Human Retinal Pigment Epithelial Cells in Culture [J]. J Biol Chem,2016, 291(25):12930-12942.
[8] Bourne MC,Campbell DA,Tansley K. Hereditary degeneration of the rat retina [J]. Br J Ophthalmol,1938,22(10):613-623.
[9] Neuhardt TH,May CA,Wilsch C,et al. Morphological changes of retinal pigment epithelium and choroid in rd-mice [J]. Exp Eye Res,1999,68(1):75-83.
[10] Lue CL. Rod cell activity in retinal degenerative rats [J]. J Formos Med Assoc,1994,93(7):605-610.
[11] Strauss O,Stumpff F,Mergler S,et al. The Royal College of Surgeons rat:an animal model for inherited retinal degeneration with a still unknown genetic defect [J]. Acta Anat,1998,162(2/3):101-111.
[12] D′Cruz PM,Yasumura D,Weir J,et al. Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat [J]. Hum Mol Genet,2000,9(4):645-651.
[13] Niemann S,Müller U. Mutations in SDHC cause autosomal dominant paraganglioma,type 3 [J]. Nat Genet,2000, 26(3):268-270.
[14] Strauch A,Haslbeck M. The function of small heat-shock proteins and their implication in proteostasis [J]. Essays Biochem,2016,60(2):163-172.
[15] Alge CS,Priglinger SG. Retinal pigment epithelium is protected against apoptosis by alpha B-crystalline [J]. Invest Ophthalmol Vis Sic,2002,43(11):3575-3582.
[16] Mehlen P,Schulze-Osthoff K,Arrigo AP. Small stress proteins as novel regulators of apoptosis. Heat shock protein 27 blocks Fas/APO-1- and staurosporine-induced cell death [J]. J Biol Chem,1996,271(28):16510-16514.
[17] 彭清华,罗萍,江晓芬,等.视网膜色素变性血淤机理的初步研究[J].国医论坛,1993(1):37-40.
[18] 彭清华,李传课.视网膜色素变性虚中夹瘀的机理研究小结[J].中国医药学报,1993,8(6):7-10.
[19] 彭清华,胡欣平,曾自明,等.视网膜色素变性辨证论治与血清性激素关系的初步研究[J].中国中医眼科杂志,1993,3(2):18-21.
[20] 徐剑.基于RHO、XBP1、Caspase12表达探讨枸杞、丹参对虚中夹瘀证RP模型大鼠的干预研究[D].长沙:湖南中医药大学,2016. |
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