-
Something wrong with this record ?
Intestinal single-pass in situ perfusion technique in rat: the influence of L-carnitine on absorption of 7-methoxytacrine
M. Kunes, Z. Svoboda, J. Kvĕtina, V. Herout, J. Herink, J. Bajgar
Language English Country Czech Republic
Document type Journal Article
Grant support
NR7935
MZ0
CEP Register
Digital library NLK
Full text - Část
Source
NLK
Directory of Open Access Journals
from 2001
Free Medical Journals
from 1998
ROAD: Directory of Open Access Scholarly Resources
from 2001
PubMed
16601805
DOI
10.5507/bp.2005.075
Knihovny.cz E-resources
- MeSH
- Cholinesterase Inhibitors pharmacokinetics MeSH
- Intestinal Absorption drug effects MeSH
- Carnitine pharmacology MeSH
- Rats MeSH
- Perfusion methods MeSH
- Rats, Wistar MeSH
- Tacrine analogs & derivatives pharmacokinetics MeSH
- Vitamin B Complex pharmacology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
7-Methoxytacrine (7-MEOTA) is an acetylcholine-esterase inhibitor that is potentially useful in the therapy of some neurodegenerative disorders. L-carnitine (CRT) is a naturally occuring compound that is known to increase penetration of some compounds through biological barriers. Aim of this study was how CRT influenced transintestinal absorption transport 7-MEOTA in rat using single-pass intestinal in situ perfusion method. The rate of absorption of 7-MEOTA during luminal perfusion with single 7-MEOTA was compared with rate of absorption during simultaneous perfusion with 7-MEOTA and CRT and with absorption rate after the premedication with CRT for period of three days before beginning of perfusion. The methodical system was the perfusion of mesenterial bed (from arteria mesenterica superior to vena portae) and intestinal luminal perfusion (from duodenum to ileum). The lower transintestinal absorption in the course of simultaneously administration of CRT than just in case of perfusion with single 7-MEOTA has been found. On the contrary a significantly higher absorption of 7-MEOTA has been noted in group of rats premedicated with CRT for three consecutive days. The interpretation suggested that molecules of CRT incorporated into the metabolism of intestinal cells facilitated transport of 7-MEOTA (as a representative substance which is at least partly transferred by carrier mechanism). In case of simultaneous luminal perfusion with CRT and 7-MEOTA competitive over-saturation of carrier systems is probably.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13003723
- 003
- CZ-PrNML
- 005
- 20130913104515.0
- 007
- ta
- 008
- 130128s2005 xr d f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.5507/bp.2005.075 $2 doi
- 035 __
- $a (PubMed)16601805
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Kuneš, Martin $7 xx0081968 $u Institute of Experimental Biopharmaceutics, Joint Research Center of PRO.MED.CS Praha a.s. and Academy of Sciences of the Czech Republic, Hradec Králové
- 245 10
- $a Intestinal single-pass in situ perfusion technique in rat: the influence of L-carnitine on absorption of 7-methoxytacrine / $c M. Kunes, Z. Svoboda, J. Kvĕtina, V. Herout, J. Herink, J. Bajgar
- 520 9_
- $a 7-Methoxytacrine (7-MEOTA) is an acetylcholine-esterase inhibitor that is potentially useful in the therapy of some neurodegenerative disorders. L-carnitine (CRT) is a naturally occuring compound that is known to increase penetration of some compounds through biological barriers. Aim of this study was how CRT influenced transintestinal absorption transport 7-MEOTA in rat using single-pass intestinal in situ perfusion method. The rate of absorption of 7-MEOTA during luminal perfusion with single 7-MEOTA was compared with rate of absorption during simultaneous perfusion with 7-MEOTA and CRT and with absorption rate after the premedication with CRT for period of three days before beginning of perfusion. The methodical system was the perfusion of mesenterial bed (from arteria mesenterica superior to vena portae) and intestinal luminal perfusion (from duodenum to ileum). The lower transintestinal absorption in the course of simultaneously administration of CRT than just in case of perfusion with single 7-MEOTA has been found. On the contrary a significantly higher absorption of 7-MEOTA has been noted in group of rats premedicated with CRT for three consecutive days. The interpretation suggested that molecules of CRT incorporated into the metabolism of intestinal cells facilitated transport of 7-MEOTA (as a representative substance which is at least partly transferred by carrier mechanism). In case of simultaneous luminal perfusion with CRT and 7-MEOTA competitive over-saturation of carrier systems is probably.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a karnitin $x farmakologie $7 D002331
- 650 _2
- $a cholinesterasové inhibitory $x farmakokinetika $7 D002800
- 650 _2
- $a intestinální absorpce $x účinky léků $7 D007408
- 650 _2
- $a perfuze $x metody $7 D010477
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a takrin $x analogy a deriváty $x farmakokinetika $7 D013619
- 650 _2
- $a vitamin B komplex $x farmakologie $7 D014803
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Svoboda, Zbyněk $7 xx0081965 $u Institute of Experimental Biopharmaceutics, Joint Research Center of PRO.MED.CS Praha a.s. and Academy of Sciences of the Czech Republic, Hradec Králové
- 700 1_
- $a Květina, Jaroslav, $d 1930- $7 jk01071205 $u Institute of Experimental Biopharmaceutics, Joint Research Center of PRO.MED.CS Praha a.s. and Academy of Sciences of the Czech Republic, Hradec Králové
- 700 1_
- $a Herout, Vladimír, $d 1925-2008 $7 jk01040876 $u Institute of Experimental Biopharmaceutics, Joint Research Center of PRO.MED.CS Praha a.s. and Academy of Sciences of the Czech Republic, Hradec Králové
- 700 1_
- $a Herink, Josef, $d 1942- $7 jx20040423003 $u Institute of Experimental Biopharmaceutics, Joint Research Center of PRO.MED.CS Praha a.s. and Academy of Sciences of the Czech Republic, Hradec Králové
- 700 1_
- $a Bajgar, Jiří, $d 1944- $7 js20020122033 $u Faculty of Military Health Sciences, University of Defence, Hradec Králové
- 773 0_
- $w MED00012606 $t Biomedical papers of the Medical Faculty of the University Palacký, Olomouc, Czech Republic $x 1213-8118 $g Roč. 149, č. 2 (2005), s. 433-435
- 910 __
- $a ABA008 $b A 1502 $c sign $y 3 $z 0
- 990 __
- $a 20130128 $b ABA008
- 991 __
- $a 20130913105013 $b ABA008
- 999 __
- $a ok $b bmc $g 966379 $s 801918
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2005 $b 149 $c 2 $d 433-435 $i 1213-8118 $m Biomedical papers of the Medical Faculty of the University Palacký, Olomouc Czech Republic $n Biomed. Pap. Fac. Med. Palacký Univ. Olomouc Czech Repub. (Print) $x MED00012606
- GRA __
- $a NR7935 $p MZ0
- LZP __
- $b NLK111 $a Pubmed-20130128