-
Je něco špatně v tomto záznamu ?
Melatonin inhibits prostaglandin E2- and sodium nitroprusside-induced ion secretion in rat distal colon
L Mrnka, M Hock, M Rybova, J Pacha
Jazyk angličtina Země Nizozemsko
NLK
ScienceDirect (archiv)
od 1993-01-01 do 2009-12-31
- MeSH
- AMP cyklický fyziologie MeSH
- dinoproston farmakologie MeSH
- financování organizované MeSH
- iontový transport účinky léků MeSH
- kolon sekrece účinky léků MeSH
- krysa rodu rattus MeSH
- melatonin farmakologie MeSH
- nitroprusid farmakologie MeSH
- potkani Wistar MeSH
- receptor melatoninový MT1 fyziologie účinky léků MeSH
- tetrodotoxin farmakologie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- zvířata MeSH
Although the gastrointestinal tract is a rich source of melatonin and possesses numerous melatonin-binding sites, the role of melatonin in this tissue has not yet been fully elucidated. In this work we focused on the role of melatonin in the modulation of ion transport in rat distal colon. Whereas melatonin had no effect on colonic secretion or caused only infrequent and small changes in the short circuit current (Isc) due to its solvent ethanol, this mediator significantly modulated the secretion elicited by some secretagogues. Out of the five substances tested (prostaglandin E(2); 5-hydroxytryptamine; bethanechol; histamine; sodium nitroprusside) melatonin inhibited the effect of prostaglandin E(2) (PGE(2)) and sodium nitroprusside (SNP). Melatonin concentration-dependently decreased PGE(2)-evoked Isc and this inhibitory effect was more obvious from the mucosal side. The basal level of cAMP in colonic mucosa was not influenced by melatonin, but this drug prevented a PGE(2)-induced increase in the level of cAMP. The neurotoxin tetrodotoxin blocked the inhibitory effect of melatonin on SNP-induced Isc. Our data suggests that melatonin takes part in the modulation of colonic ion transport. The modulatory effect of melatonin on PGE(2)-induced Isc occurs directly at the level of the epithelium, whereas the effect on SNP-induced Isc is indirect and located in tetrodotoxin-sensitive enteric neurons.
- 000
- 03025naa 2200409 a 4500
- 001
- bmc11002993
- 003
- CZ-PrNML
- 005
- 20130601111404.0
- 008
- 110225s2008 ne e eng||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Mrnka, Libor. $7 _BN001217
- 245 10
- $a Melatonin inhibits prostaglandin E2- and sodium nitroprusside-induced ion secretion in rat distal colon / $c L Mrnka, M Hock, M Rybova, J Pacha
- 314 __
- $a Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic. gibor@tiscali.cz
- 520 9_
- $a Although the gastrointestinal tract is a rich source of melatonin and possesses numerous melatonin-binding sites, the role of melatonin in this tissue has not yet been fully elucidated. In this work we focused on the role of melatonin in the modulation of ion transport in rat distal colon. Whereas melatonin had no effect on colonic secretion or caused only infrequent and small changes in the short circuit current (Isc) due to its solvent ethanol, this mediator significantly modulated the secretion elicited by some secretagogues. Out of the five substances tested (prostaglandin E(2); 5-hydroxytryptamine; bethanechol; histamine; sodium nitroprusside) melatonin inhibited the effect of prostaglandin E(2) (PGE(2)) and sodium nitroprusside (SNP). Melatonin concentration-dependently decreased PGE(2)-evoked Isc and this inhibitory effect was more obvious from the mucosal side. The basal level of cAMP in colonic mucosa was not influenced by melatonin, but this drug prevented a PGE(2)-induced increase in the level of cAMP. The neurotoxin tetrodotoxin blocked the inhibitory effect of melatonin on SNP-induced Isc. Our data suggests that melatonin takes part in the modulation of colonic ion transport. The modulatory effect of melatonin on PGE(2)-induced Isc occurs directly at the level of the epithelium, whereas the effect on SNP-induced Isc is indirect and located in tetrodotoxin-sensitive enteric neurons.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a kolon $x sekrece $x účinky léků $7 D003106
- 650 _2
- $a AMP cyklický $x fyziologie $7 D000242
- 650 _2
- $a dinoproston $x farmakologie $7 D015232
- 650 _2
- $a vztah mezi dávkou a účinkem léčiva $7 D004305
- 650 _2
- $a iontový transport $x účinky léků $7 D017136
- 650 _2
- $a melatonin $x farmakologie $7 D008550
- 650 _2
- $a nitroprusid $x farmakologie $7 D009599
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a receptor melatoninový MT1 $x fyziologie $x účinky léků $7 D044122
- 650 _2
- $a tetrodotoxin $x farmakologie $7 D013779
- 650 _2
- $a financování organizované $7 D005381
- 700 1_
- $a Hock, Miroslav $7 xx0170860
- 700 1_
- $a Rybová, Markéta. $7 _BN001215
- 700 1_
- $a Pácha, Jiří $7 xx0030583
- 773 0_
- $t European Journal of Pharmacology $w MED00001641 $g Roč. 581, č. 1-2 (2008), s. 164-170 $x 0014-2999
- 910 __
- $a ABA008 $b x $y 1
- 990 __
- $a 20110413113604 $b ABA008
- 991 __
- $a 20130601111737 $b ABA008
- 999 __
- $a ok $b bmc $g 830398 $s 694985
- BAS __
- $a 3
- BMC __
- $a 2008 $b 581 $c 1-2 $d 164-170 $i 0014-2999 $m European journal of pharmacology $n Eur J Pharmacol $x MED00001641
- LZP __
- $a 2011-2B/dkme