Ananth Sudha, Karunakaran Senthil, Martin Pamela M, Nagineni Chandrasekharam N, Hooks John J, Smith Sylvia B, Prasad Puttur D, Ganapathy Vadivel
Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, Georgia 30912, USA.
Pharm Res. 2009 May;26(5):1226-35. doi: 10.1007/s11095-008-9709-x. Epub 2008 Sep 10.
To investigate whether conjunctival epithelial cells express transport processes for opioid peptides.
We monitored the uptake of [(3)H]deltorphin II and [(3)H]DADLE, two hydrolysis-resistant synthetic opioid peptides, in the rabbit conjunctival epithelial cell line CJVE and elucidated the characteristics of the uptake process.
CJVE cells express robust uptake activity for deltorphin II and DADLE. Both opioid peptides compete with each other for transport. Several endogenous and synthetic opioid peptides, but not non-peptide opioid antagonists, are recognized by the transport process. Though various peptides inhibit the uptake of deltorphin II and DADLE in a similar manner, the uptake of deltorphin II is partly Na(+)-dependent whereas that of DADLE mostly Na(+)-independent. The transport process shows high affinity for many endogenous/synthetic opioid peptides. Functional features reveal that this transport process may be distinct from the opioid peptide transport system described in the retinal pigment epithelial cell line ARPE-19 and also from the organic anion transporting polypeptides, which are known to transport opioid peptides.
CJVE cells express a novel, hitherto unknown transport process for endogenous/synthetic opioid peptides. This new transport process may offer an effective delivery route for opioid peptide drugs to the posterior segment of the eye.
研究结膜上皮细胞是否表达阿片肽的转运过程。
我们监测了兔结膜上皮细胞系CJVE对两种抗水解的合成阿片肽[³H]强啡肽II和[³H]DADLE的摄取,并阐明了摄取过程的特征。
CJVE细胞对强啡肽II和DADLE表现出强大的摄取活性。两种阿片肽相互竞争转运。几种内源性和合成阿片肽可被该转运过程识别,但非肽类阿片拮抗剂则不能。尽管各种肽以类似方式抑制强啡肽II和DADLE的摄取,但强啡肽II的摄取部分依赖于Na⁺,而DADLE的摄取大多不依赖于Na⁺。该转运过程对许多内源性/合成阿片肽具有高亲和力。功能特性表明,该转运过程可能不同于视网膜色素上皮细胞系ARPE - 19中描述的阿片肽转运系统,也不同于已知可转运阿片肽的有机阴离子转运多肽。
CJVE细胞表达一种新的、迄今未知的内源性/合成阿片肽转运过程。这种新的转运过程可能为阿片肽药物向眼后段提供一种有效的递送途径。