The effect of methylated β-cyclodextrins on the tight junctions of the rat nasal respiratory epithelium:: Electron microscopic and confocal laser scanning microscopic visualization studies

被引:39
作者
Marttin, E
Verhoef, JC
Spies, F
van der Meulen, J
Nagelkerke, JF
Koerten, HK
Merkus, FWHM
机构
[1] Leiden Amsterdam Ctr Drug Res, Div Pharmaceut Technol & Biopharmaceut, NL-2300 RA Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Electron Microscopy Lab, NL-2300 RA Leiden, Netherlands
[3] Leiden Amsterdam Ctr Drug Res, Div Toxicol, NL-2300 RA Leiden, Netherlands
关键词
electron microscopy; confocal laser scanning microscopy; nasal drug delivery; cyclodextrins; sodium taurodihydrofusidate; tight junctions;
D O I
10.1016/S0168-3659(98)00115-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The nasal absorption enhancer randomly methylated beta-cyclodextrin (RAMEB) is thought to increase the paracellular permeability of the nasal epithelium by opening of the tight junctions. The effects of RAMEB on the cytoskeleton of the rat nasal epithelium in vivo were determined by confocal laser scanning microscopy (CLSM). The effects on the tight junctions of the rat nasal epithelium were also investigated, using transmission electron microscopy (TEM) of thin sections. The effects of RAMEB were compared with those of the absorption enhancer sodium taurodihydrofusidate (STDHF). Fifteen minutes after nasal administration of 2% RAMEB in vivo, the distribution of cytoskeletal actin was comparable to the untreated control, suggesting that RAMEB does not cause opening of the tight junctions via cytoskeletal interactions. In contrast, administration of 1% STDHF resulted in changes in the actin staining. Furthermore, with TEM severe damage of the nasal epithelium was observed after treatment with 1% STDHF. Ultrastructural changes of the tight junctions were not apparent in TEM sections after treatment with 2% RAMEB. In conclusion, CLSM and TEM are suitable methods to visualize the effects of absorption enhancers on nasal epithelial morphology. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:205 / 213
页数:9
相关论文
共 30 条
[1]   SODIUM CAPRATE ELICITS DILATATIONS IN HUMAN INTESTINAL TIGHT JUNCTIONS AND ENHANCES DRUG ABSORPTION BY THE PARACELLULAR ROUTE [J].
ANDERBERG, EK ;
LINDMARK, T ;
ARTURSSON, P .
PHARMACEUTICAL RESEARCH, 1993, 10 (06) :857-864
[2]   TIGHT JUNCTIONS AND THE MOLECULAR-BASIS FOR REGULATION OF PARACELLULAR PERMEABILITY [J].
ANDERSON, JM ;
VANITALLIE, CM .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1995, 269 (04) :G467-G475
[3]   THE EFFECT OF SODIUM TAURO-24,25-DIHYDROFUSIDATE ON THE NASAL ABSORPTION OF HUMAN GROWTH-HORMONE IN 3 ANIMAL-MODELS [J].
BALDWIN, PA ;
KLINGBEIL, CK ;
GRIMM, CJ ;
LONGENECKER, JP .
PHARMACEUTICAL RESEARCH, 1990, 7 (05) :547-552
[4]   STARCH MICROSPHERES INDUCE PULSATILE DELIVERY OF DRUGS AND PEPTIDES ACROSS THE EPITHELIAL BARRIER BY REVERSIBLE SEPARATION OF THE TIGHT JUNCTIONS [J].
BJORK, E ;
ISAKSSON, U ;
EDMAN, P ;
ARTURSSON, P .
JOURNAL OF DRUG TARGETING, 1995, 2 (06) :501-507
[6]   FRACTURE FACES OF ZONULAE OCCLUDENTES FROM TIGHT AND LEAKY EPITHELIA [J].
CLAUDE, P ;
GOODENOUGH, DA .
JOURNAL OF CELL BIOLOGY, 1973, 58 (02) :390-400
[7]  
FUJIMOTO K, 1995, J CELL SCI, V108, P3443
[8]   OCCLUDIN - A NOVEL INTEGRAL MEMBRANE-PROTEIN LOCALIZING AT TIGHT JUNCTIONS [J].
FURUSE, M ;
HIRASE, T ;
ITOH, M ;
NAGAFUCHI, A ;
YONEMURA, S ;
TSUKITA, S ;
TSUKITA, S .
JOURNAL OF CELL BIOLOGY, 1993, 123 (06) :1777-1788
[9]  
GUMBINER B, 1987, AM J PHYSIOL, V253, P749
[10]   BREAKING THROUGH THE TIGHT JUNCTION BARRIER [J].
GUMBINER, BM .
JOURNAL OF CELL BIOLOGY, 1993, 123 (06) :1631-1633