Effects of porcine relaxin on contraction, membrane response and cyclic AMP content in rat myometrium in comparison with the effects of isoprenaline and forskolin

Takuro Osa, Hiroyoshi Inoue, Koji Okabe

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Abstract

The longitudinal muscle from the uterus of oestrogen‐treated rats was quiescent in Mg‐free Krebs solution. Electrical stimulation generated phasic contraction, which was depressed to 35% and 18% by 50 mu and 150 mu porcine relaxin, respectively. The phasic contractions were more strongly depressed to 26% by 50 mu relaxin in solution containing 0.6 mm Mg, and the depression lasted for more than 4 h after the removal of relaxin. During the persisting depression, raising the external Ca to 7.5 mm did not restore the contraction, but the contraction was restored by removal of Mg. The depression of the phasic contraction by relaxin, examined in Mg‐free solution, was enhanced and reduced by pretreatment of the tissue with 0.6 mm Mg and 0.6 mm Mn, respectively, for about 15 min. In contrast, the depression of contraction by isoprenaline or forskolin was enhanced by pretreatment with either Mg or Mn. The cellular content of cyclic AMP was measured in Krebs solution containing 0.6 mm Mg. The values were 1.24 (pmol mg−1 protein) in control solution, and 2.31 and 1.56 when the tissues were treated with 150 mu relaxin and 10−9 m isoprenaline, respectively. The cyclic AMP production in response to 10−7 m forskolin measured in Mg‐free solution was enhanced when the tissue was pretreated with either 0.6 mm Mg or Mn for 15 min. The cyclic AMP production in response to 100 mu relaxin was increased when the tissue was pretreated with 0.6 mm Mg, and was unchanged by pretreatment with Mn. The cyclic AMP production in response to 10−9 m isoprenaline was unchanged by pretreatment with the divalent cations. The membrane potential of the muscle was −60.8 mV in Krebs solution containing 0.3 mm Mg, and electrical stimulation induced an action potential which consisted of spike and plateau components. Application of 150 mu relaxin reduced the duration of the plateau; the contractions were progressively depressed. The resting membrane potential and membrane resistance were unchanged by application of 150 mu relaxin. The membrane was hyperpolarized by 2.8 mV, accompanied by a decrease in membrane resistance, when 10−9 m isoprenaline was applied. Although there were several differences between the effects of relaxin and isoprenaline, it is probable that some process, which is cyclic AMP‐dependent, accelerated by Mg and depressed by Mn, is involved in the depressant action of relaxin on contraction. 1991 British Pharmacological Society

Original languageEnglish
Pages (from-to)950-960
Number of pages11
JournalBritish Journal of Pharmacology
Volume104
Issue number4
DOIs
Publication statusPublished - 1991 Jan 1
Externally publishedYes

Fingerprint

Relaxin
Myometrium
Colforsin
Isoproterenol
Cyclic AMP
Swine
Membranes
Membrane Potentials
Electric Stimulation
Muscles
Divalent Cations
Action Potentials
Uterus

Keywords

  • cyclic AMP
  • forskolin
  • isoprenaline
  • Mg
  • Mn
  • myometrium
  • Relaxin

ASJC Scopus subject areas

  • Pharmacology

Cite this

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title = "Effects of porcine relaxin on contraction, membrane response and cyclic AMP content in rat myometrium in comparison with the effects of isoprenaline and forskolin",
abstract = "The longitudinal muscle from the uterus of oestrogen‐treated rats was quiescent in Mg‐free Krebs solution. Electrical stimulation generated phasic contraction, which was depressed to 35{\%} and 18{\%} by 50 mu and 150 mu porcine relaxin, respectively. The phasic contractions were more strongly depressed to 26{\%} by 50 mu relaxin in solution containing 0.6 mm Mg, and the depression lasted for more than 4 h after the removal of relaxin. During the persisting depression, raising the external Ca to 7.5 mm did not restore the contraction, but the contraction was restored by removal of Mg. The depression of the phasic contraction by relaxin, examined in Mg‐free solution, was enhanced and reduced by pretreatment of the tissue with 0.6 mm Mg and 0.6 mm Mn, respectively, for about 15 min. In contrast, the depression of contraction by isoprenaline or forskolin was enhanced by pretreatment with either Mg or Mn. The cellular content of cyclic AMP was measured in Krebs solution containing 0.6 mm Mg. The values were 1.24 (pmol mg−1 protein) in control solution, and 2.31 and 1.56 when the tissues were treated with 150 mu relaxin and 10−9 m isoprenaline, respectively. The cyclic AMP production in response to 10−7 m forskolin measured in Mg‐free solution was enhanced when the tissue was pretreated with either 0.6 mm Mg or Mn for 15 min. The cyclic AMP production in response to 100 mu relaxin was increased when the tissue was pretreated with 0.6 mm Mg, and was unchanged by pretreatment with Mn. The cyclic AMP production in response to 10−9 m isoprenaline was unchanged by pretreatment with the divalent cations. The membrane potential of the muscle was −60.8 mV in Krebs solution containing 0.3 mm Mg, and electrical stimulation induced an action potential which consisted of spike and plateau components. Application of 150 mu relaxin reduced the duration of the plateau; the contractions were progressively depressed. The resting membrane potential and membrane resistance were unchanged by application of 150 mu relaxin. The membrane was hyperpolarized by 2.8 mV, accompanied by a decrease in membrane resistance, when 10−9 m isoprenaline was applied. Although there were several differences between the effects of relaxin and isoprenaline, it is probable that some process, which is cyclic AMP‐dependent, accelerated by Mg and depressed by Mn, is involved in the depressant action of relaxin on contraction. 1991 British Pharmacological Society",
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T1 - Effects of porcine relaxin on contraction, membrane response and cyclic AMP content in rat myometrium in comparison with the effects of isoprenaline and forskolin

AU - Osa, Takuro

AU - Inoue, Hiroyoshi

AU - Okabe, Koji

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N2 - The longitudinal muscle from the uterus of oestrogen‐treated rats was quiescent in Mg‐free Krebs solution. Electrical stimulation generated phasic contraction, which was depressed to 35% and 18% by 50 mu and 150 mu porcine relaxin, respectively. The phasic contractions were more strongly depressed to 26% by 50 mu relaxin in solution containing 0.6 mm Mg, and the depression lasted for more than 4 h after the removal of relaxin. During the persisting depression, raising the external Ca to 7.5 mm did not restore the contraction, but the contraction was restored by removal of Mg. The depression of the phasic contraction by relaxin, examined in Mg‐free solution, was enhanced and reduced by pretreatment of the tissue with 0.6 mm Mg and 0.6 mm Mn, respectively, for about 15 min. In contrast, the depression of contraction by isoprenaline or forskolin was enhanced by pretreatment with either Mg or Mn. The cellular content of cyclic AMP was measured in Krebs solution containing 0.6 mm Mg. The values were 1.24 (pmol mg−1 protein) in control solution, and 2.31 and 1.56 when the tissues were treated with 150 mu relaxin and 10−9 m isoprenaline, respectively. The cyclic AMP production in response to 10−7 m forskolin measured in Mg‐free solution was enhanced when the tissue was pretreated with either 0.6 mm Mg or Mn for 15 min. The cyclic AMP production in response to 100 mu relaxin was increased when the tissue was pretreated with 0.6 mm Mg, and was unchanged by pretreatment with Mn. The cyclic AMP production in response to 10−9 m isoprenaline was unchanged by pretreatment with the divalent cations. The membrane potential of the muscle was −60.8 mV in Krebs solution containing 0.3 mm Mg, and electrical stimulation induced an action potential which consisted of spike and plateau components. Application of 150 mu relaxin reduced the duration of the plateau; the contractions were progressively depressed. The resting membrane potential and membrane resistance were unchanged by application of 150 mu relaxin. The membrane was hyperpolarized by 2.8 mV, accompanied by a decrease in membrane resistance, when 10−9 m isoprenaline was applied. Although there were several differences between the effects of relaxin and isoprenaline, it is probable that some process, which is cyclic AMP‐dependent, accelerated by Mg and depressed by Mn, is involved in the depressant action of relaxin on contraction. 1991 British Pharmacological Society

AB - The longitudinal muscle from the uterus of oestrogen‐treated rats was quiescent in Mg‐free Krebs solution. Electrical stimulation generated phasic contraction, which was depressed to 35% and 18% by 50 mu and 150 mu porcine relaxin, respectively. The phasic contractions were more strongly depressed to 26% by 50 mu relaxin in solution containing 0.6 mm Mg, and the depression lasted for more than 4 h after the removal of relaxin. During the persisting depression, raising the external Ca to 7.5 mm did not restore the contraction, but the contraction was restored by removal of Mg. The depression of the phasic contraction by relaxin, examined in Mg‐free solution, was enhanced and reduced by pretreatment of the tissue with 0.6 mm Mg and 0.6 mm Mn, respectively, for about 15 min. In contrast, the depression of contraction by isoprenaline or forskolin was enhanced by pretreatment with either Mg or Mn. The cellular content of cyclic AMP was measured in Krebs solution containing 0.6 mm Mg. The values were 1.24 (pmol mg−1 protein) in control solution, and 2.31 and 1.56 when the tissues were treated with 150 mu relaxin and 10−9 m isoprenaline, respectively. The cyclic AMP production in response to 10−7 m forskolin measured in Mg‐free solution was enhanced when the tissue was pretreated with either 0.6 mm Mg or Mn for 15 min. The cyclic AMP production in response to 100 mu relaxin was increased when the tissue was pretreated with 0.6 mm Mg, and was unchanged by pretreatment with Mn. The cyclic AMP production in response to 10−9 m isoprenaline was unchanged by pretreatment with the divalent cations. The membrane potential of the muscle was −60.8 mV in Krebs solution containing 0.3 mm Mg, and electrical stimulation induced an action potential which consisted of spike and plateau components. Application of 150 mu relaxin reduced the duration of the plateau; the contractions were progressively depressed. The resting membrane potential and membrane resistance were unchanged by application of 150 mu relaxin. The membrane was hyperpolarized by 2.8 mV, accompanied by a decrease in membrane resistance, when 10−9 m isoprenaline was applied. Although there were several differences between the effects of relaxin and isoprenaline, it is probable that some process, which is cyclic AMP‐dependent, accelerated by Mg and depressed by Mn, is involved in the depressant action of relaxin on contraction. 1991 British Pharmacological Society

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