1985
DOI: 10.1016/0306-3623(85)90192-2
|View full text |Cite
|
Sign up to set email alerts
|

Relation between inhibition of calmodulin and mediator release from rat mast cells

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
4
0
1

Year Published

1988
1988
1991
1991

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 15 publications
(5 citation statements)
references
References 24 publications
0
4
0
1
Order By: Relevance
“…Concentrations of 100 ~tM or higher released histamine by themselves in both species [4]. It could be shown that this histamine release is due to cytotoxic effects, since LDH liberation was reported to parallel the histamine release [5]. Our data show that W5 inhibited the Con A-induced histamine release about 4 times less potently than W7 and about 10 times less potently than TFPr.…”
Section: Discussionmentioning
confidence: 64%
See 1 more Smart Citation
“…Concentrations of 100 ~tM or higher released histamine by themselves in both species [4]. It could be shown that this histamine release is due to cytotoxic effects, since LDH liberation was reported to parallel the histamine release [5]. Our data show that W5 inhibited the Con A-induced histamine release about 4 times less potently than W7 and about 10 times less potently than TFPr.…”
Section: Discussionmentioning
confidence: 64%
“…Our data show that W5 inhibited the Con A-induced histamine release about 4 times less potently than W7 and about 10 times less potently than TFPr. The ICso of the calcium dependent phosphodiesterase (PDE) inhibition as an index for calmodulin antagonism was found to be 270 laM for W5, 38 laM for W7 [5] and 28 btM for TFPr [6]. Hence the ratios of concentrations for inhibition of PDE and histamine release are about equal.…”
Section: Discussionmentioning
confidence: 99%
“…Nifedipine and related 1,4-dihydropyridines (DHP) exhibit potent and selective inhibitory actions on voltagesensitive calcium channels of the L-type (Spedding, 1987;Fleckenstein, 1985;Doyle, 1984). The purpose of our study was to investigate the effect of nifedipine (Bay A 10401, nisoldipine (Bay K 55521, and nitrendipine (Bay E 5009) on 45Ca uptake activated with 4-aminopyridin, a pharmacological agent which blocks K + channels (Ohishi et al, 1985). We found that 4-aminiopyridin activated 45Ca uptake in mast cells as did other Kf blockers such as quinine and sparteine (submitted data).…”
mentioning
confidence: 91%
“…The purpose of our study was to investigate the effect of nifedipine (Bay A 10401, nisoldipine (Bay K 55521, and nitrendipine (Bay E 5009) on 45Ca uptake activated with 4-aminopyridin, a pharmacological agent which blocks K + channels (Ohishi et al, 1985). We found that 4-aminiopyridin activated 45Ca uptake in mast cells as did other Kf blockers such as quinine and sparteine (submitted data).…”
mentioning
confidence: 93%
“…A maioria de suas ações é dependente de proteínas de ligação, que tem como função, intermediar o cálcio e a proteína a ser regulada, sendo a calmodulina, um dos exemplos mais marcantes. A interação cálcio-calmodulina participa na secreção de grânulos por mastócitos (Ohishi et al, 1985), ativação e migração de monócitos, macrófagos e neutrófilos (Singh e Sodhi, 1999;Hu et al, 2000), e na produção de NO por enzima constitutiva (Koyama et al, 2002).…”
Section: Bradicinina -Mediador Da Produção De No Por Células Endoteliaisunclassified