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[利用人Caco-2细胞单层研究盐酸黄连碱和小檗红碱在人肠道上皮细胞中的吸收]

[Absorption of coptisine chloride and berberrubine across human intestinal epithelial by using human Caco-2 cell monolayers].

作者信息

Ma Lian, Yang Xiu-Wei

机构信息

Department of Natural Medicines, State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100083, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2007 Dec;32(23):2523-7.

Abstract

OBJECTIVE

To study the absorption of coptisine chloride (COP) and berberrubine (BRB) as chemical constituents of some traditional Chinese medicines in human intestinal epithelial.

METHOD

By using Caco-2 (the human colonic adenocarcinoma cell lines) cell monolayers as an intestinal epithelial cell model, the permeability of COP and BRB were studied from apical side (AP side) to basolateral side (BL side) or from BL side to AP side. The two alkaloids were measured by reversed-phase high performance liquid chromatography (HPLC) coupled with UV detector. Transport parameters and apparent permeability coefficients (P(app)) were then calculated and compared with those of propranolol and atenolol. P(app) values were also compared with the reported values for model compounds (propranolol and atenolol).

RESULT

The P(app) values of COP, BRB were (1.103 +/- 0.162) x 10(-5), (1.309 +/- 0.102) x 10(-5) cm x s(-1 from AP side to BL side, and (0.300 +/- 0.041) x 10(-5) and (1.955 +/- 0.055) x 10(-5) cm x s(-1) from BL side to AP side, respectively. Their P(app) values were identical with those of propranolol [(2.23 +/- 0.10) x 10(-5 cm x s(-1)], which is a transcellular transport marker and as a control substance for high permeability. On the other hand, the efflux transport of BRB was higher 1.49 times more than its influx transport with 0.67 rate of P(app A-->B)/P(app B-->A). But P(app A-->B)/P(app B-->A value of COP was 3.67, which suggested that the efflux transport have not been involved in its absorbed mechanism in Caco-2 cells monolayers.

CONCLUSION

COP and BRB can be absorbed across intestinal epithelial cells, and they are completely absorbed compounds. BRB may have been involved in efflux mechanism in Caco-2 cells monolayers model from the basolateral-to-apical direction.

摘要

目的

研究作为一些传统中药化学成分的盐酸小檗碱(COP)和小檗红碱(BRB)在人肠上皮细胞中的吸收情况。

方法

以Caco-2(人结肠腺癌细胞系)细胞单层作为肠上皮细胞模型,研究COP和BRB从顶端侧(AP侧)到基底外侧侧(BL侧)或从BL侧到AP侧的通透性。采用反相高效液相色谱(HPLC)结合紫外检测器测定这两种生物碱。然后计算转运参数和表观渗透系数(P(app)),并与普萘洛尔和阿替洛尔的进行比较。P(app)值也与模型化合物(普萘洛尔和阿替洛尔)的报道值进行比较。

结果

COP、BRB从AP侧到BL侧的P(app)值分别为(1.103±0.162)×10⁻⁵、(1.309±0.102)×10⁻⁵ cm·s⁻¹,从BL侧到AP侧的P(app)值分别为(0.300±0.041)×10⁻⁵和(1.955±0.055)×10⁻⁵ cm·s⁻¹。它们的P(app)值与普萘洛尔[(2.23±0.10)×10⁻⁵ cm·s⁻¹]相同,普萘洛尔是一种跨细胞转运标志物,用作高通透性对照物质。另一方面,BRB的外排转运比其入胞转运高1.49倍,P(app A→B)/P(app B→A)比值为0.67。但COP的P(app A→B)/P(app B→A)值为3.67,这表明在Caco-2细胞单层中外排转运未参与其吸收机制。

结论

COP和BRB可通过肠上皮细胞吸收,且它们是完全吸收的化合物。在Caco-2细胞单层模型中,BRB可能从基底外侧向顶端方向参与了外排机制。

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