Literature DB >> 2732951

Effect of forskolin on cytosolic Ca++ level and contraction in vascular smooth muscle.

A Abe1, H Karaki.   

Abstract

The effects of forskolin, an activator of adenylate cyclase, on cytoplasmic Ca++ level ([Ca++]cyt) measured simultaneously with muscle tension using fura-2-Ca++ fluorescence were examined in isolated smooth muscle of rat aorta. Forskolin decreased muscle tension and [Ca++]cyt in resting aorta whereas both norepinephrine and high K+ solution produced sustained increase in muscle tension and [Ca++]cyt. Addition of forskolin during the sustained contractions decreased muscle tension more strongly than [Ca++]cyt. Norepinephrine-induced contraction was more sensitive to forskolin than high K+-induced contraction. The inhibitory effect of forskolin was attenuated when the concentration of norepinephrine or K+ was increased. Cumulative addition of norepinephrine or K+ induced a concentration-dependent increase in both [Ca++]cyt and muscle tension and a positive [Ca++]cyt-tension correlation was observed. In the presence of 0.1 microM forskolin, the norepinephrine-induced increments in [Ca++]cyt and muscle tension were inhibited without changing the [Ca++]cyt-tension relationship. In the presence of a higher concentration (1 microM) of forskolin, muscle tension was inhibited more strongly with only a small additional decrease in [Ca++]cyt resulting in a shift of the [Ca++]cyt-tension relationship. Norepinephrine induced transient increments in [Ca++]cyt and muscle tension in Ca++-free solution and forskolin inhibited these changes. These results suggest that forskolin has concentration-dependent inhibitory effects on vascular contractility to decrease [Ca++]cyt at lower concentrations and to decrease the sensitivity of contractile elements to Ca++ at higher concentrations.

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Year:  1989        PMID: 2732951

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  13 in total

1.  Dissociation of P2 purinoceptor-mediated increase in intracellular Ca2+ level from myosin light chain phosphorylation and contraction in rat aorta.

Authors:  S Kitajima; K Harada; M Hori; H Ozaki; H Karaki
Journal:  Br J Pharmacol       Date:  1996-06       Impact factor: 8.739

2.  Inhibitory effect of a toxin okadaic acid, isolated from the black sponge on smooth muscle and platelets.

Authors:  H Karaki; M Mitsui; H Nagase; H Ozaki; S Shibata; D Uemura
Journal:  Br J Pharmacol       Date:  1989-10       Impact factor: 8.739

3.  Effect of a novel inhibitor of cyclic AMP phosphodiesterase, E-1020, on cytosolic Ca++ level and contraction in vascular smooth muscle.

Authors:  M Tajimi; H Ozaki; K Sato; H Karaki
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1991-11       Impact factor: 3.000

4.  Force and intracellular Ca2+ during cyclic nucleotide-mediated relaxation of rat anococcygeus muscle and the effects of cyclopiazonic acid.

Authors:  G L Raymond; I R Wendt
Journal:  Br J Pharmacol       Date:  1996-11       Impact factor: 8.739

5.  Changes in cytosolic CA2+ and contraction induced by various stimulants and relaxants in canine tracheal smooth muscle.

Authors:  H Ozaki; S C Kwon; M Tajimi; H Karaki
Journal:  Pflugers Arch       Date:  1990-06       Impact factor: 3.657

6.  Protamine relaxes vascular smooth muscle by directly reducing cytosolic free calcium concentrations in small resistance arteries.

Authors:  Takashi Akata; Kenji Kodama; Alex S Evers; Shosuke Takahashi
Journal:  J Anesth       Date:  1996-12       Impact factor: 2.078

Review 7.  Ca2+ pumps in smooth muscle cells.

Authors:  L Raeymaekers; F Wuytack
Journal:  J Muscle Res Cell Motil       Date:  1993-04       Impact factor: 2.698

8.  The effect of forskolin on 5-HT1-like and angiotensin II-induced vasoconstriction and cyclic AMP content of the rabbit isolated femoral artery.

Authors:  V A Randall; S J MacLennan; G R Martin; V G Wilson
Journal:  Br J Pharmacol       Date:  1996-06       Impact factor: 8.739

9.  Cyclic AMP relaxes swine arterial smooth muscle predominantly by decreasing cell Ca2+ concentration.

Authors:  N L McDaniel; C M Rembold; H M Richard; R A Murphy
Journal:  J Physiol       Date:  1991-08       Impact factor: 5.182

10.  Inhibition of proliferation, but not of Ca2+ mobilization, by cyclic AMP and GMP in rabbit aortic smooth-muscle cells.

Authors:  J W Assender; K M Southgate; M B Hallett; A C Newby
Journal:  Biochem J       Date:  1992-12-01       Impact factor: 3.857

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