Inhibition of airway smooth muscle tone by Chinese herbal medicines

The aim of the present study was to elucidate whether Chinese traditional herbal drugs, Gorei‐San (TJ‐17) and Toki‐Shakuyaku‐San (TJ‐23), affect airway smooth muscle tone and, if so, to determine what the mechanism of action is. Rabbit tracheal segments were isolated and the contractile responses to...

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Veröffentlicht in:The European respiratory journal 2000-12, Vol.16 (6), p.1123-1128
Hauptverfasser: Tagaya, E, Tamaoki, J, Kawatani, K, Taira, M, Nagai, A
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container_issue 6
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creator Tagaya, E
Tamaoki, J
Kawatani, K
Taira, M
Nagai, A
description The aim of the present study was to elucidate whether Chinese traditional herbal drugs, Gorei‐San (TJ‐17) and Toki‐Shakuyaku‐San (TJ‐23), affect airway smooth muscle tone and, if so, to determine what the mechanism of action is. Rabbit tracheal segments were isolated and the contractile responses to electrical field stimulation and acetylcholine were measured before and after the application of TJ‐17 or TJ‐23 under isometric conditions in vitro. Ouabain‐sensitive rubidium‐86 (86Rb) uptake by tissues in response to each drug was also measured. Each herbal medicine attenuated the contractile responses to electrical field stimulation and acetylcholine in a concentration‐dependent manner, the maximal inhibition of acetylcholine‐induced contraction being 37.5±4.9% for TJ‐17 and 42.4±5.3% for TJ‐23 (p
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Rabbit tracheal segments were isolated and the contractile responses to electrical field stimulation and acetylcholine were measured before and after the application of TJ‐17 or TJ‐23 under isometric conditions in vitro. Ouabain‐sensitive rubidium‐86 (86Rb) uptake by tissues in response to each drug was also measured. Each herbal medicine attenuated the contractile responses to electrical field stimulation and acetylcholine in a concentration‐dependent manner, the maximal inhibition of acetylcholine‐induced contraction being 37.5±4.9% for TJ‐17 and 42.4±5.3% for TJ‐23 (p&lt;0.05 for each). These effects were not altered by mechanical removal of the epithelium, indomethacin, the nitric oxide synthase inhibitor NG‐nitro‐ l‐arginine methyl ester, the cyclic adenosine monophosphate (cAMP)‐dependent protein kinase inhibitor adenosine 3′5′‐cyclic monophosphorothiioate (Rp‐cAMPS), the cyclic guanosine monophosphate (cGMP)‐dependent protein kinase inhibitor KT5823, or the calcium (Ca2+)‐activated potassium (K+) channel inhibitor chary‐bdotoxin, but were greatly inhibited in the presence of the sodium (Na+)‐K+ adenosine triphosphatase (ATPase) inhibitor ouabain. Incubation of tissues with TJ‐17 and TJ‐23 dose dependently increased ouabain‐sensitive 86Rb uptake. The results of the study suggest that both Gorei‐San and Toki‐Shakuyaku‐San reduce airway smooth muscle tone via a postjunctional mechanism probably through stimulation of the sodium pump and the subsequent hyperpolarization/repolarization of the cell membrane. 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Rabbit tracheal segments were isolated and the contractile responses to electrical field stimulation and acetylcholine were measured before and after the application of TJ‐17 or TJ‐23 under isometric conditions in vitro. Ouabain‐sensitive rubidium‐86 (86Rb) uptake by tissues in response to each drug was also measured. Each herbal medicine attenuated the contractile responses to electrical field stimulation and acetylcholine in a concentration‐dependent manner, the maximal inhibition of acetylcholine‐induced contraction being 37.5±4.9% for TJ‐17 and 42.4±5.3% for TJ‐23 (p&lt;0.05 for each). These effects were not altered by mechanical removal of the epithelium, indomethacin, the nitric oxide synthase inhibitor NG‐nitro‐ l‐arginine methyl ester, the cyclic adenosine monophosphate (cAMP)‐dependent protein kinase inhibitor adenosine 3′5′‐cyclic monophosphorothiioate (Rp‐cAMPS), the cyclic guanosine monophosphate (cGMP)‐dependent protein kinase inhibitor KT5823, or the calcium (Ca2+)‐activated potassium (K+) channel inhibitor chary‐bdotoxin, but were greatly inhibited in the presence of the sodium (Na+)‐K+ adenosine triphosphatase (ATPase) inhibitor ouabain. Incubation of tissues with TJ‐17 and TJ‐23 dose dependently increased ouabain‐sensitive 86Rb uptake. The results of the study suggest that both Gorei‐San and Toki‐Shakuyaku‐San reduce airway smooth muscle tone via a postjunctional mechanism probably through stimulation of the sodium pump and the subsequent hyperpolarization/repolarization of the cell membrane. 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Drug treatments</topic><topic>Rabbits</topic><topic>Respiratory system</topic><topic>sodium‐potassium adenosine triphosphate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tagaya, E</creatorcontrib><creatorcontrib>Tamaoki, J</creatorcontrib><creatorcontrib>Kawatani, K</creatorcontrib><creatorcontrib>Taira, M</creatorcontrib><creatorcontrib>Nagai, A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The European respiratory journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tagaya, E</au><au>Tamaoki, J</au><au>Kawatani, K</au><au>Taira, M</au><au>Nagai, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of airway smooth muscle tone by Chinese herbal medicines</atitle><jtitle>The European respiratory journal</jtitle><addtitle>Eur Respir J</addtitle><date>2000-12</date><risdate>2000</risdate><volume>16</volume><issue>6</issue><spage>1123</spage><epage>1128</epage><pages>1123-1128</pages><issn>0903-1936</issn><eissn>1399-3003</eissn><abstract>The aim of the present study was to elucidate whether Chinese traditional herbal drugs, Gorei‐San (TJ‐17) and Toki‐Shakuyaku‐San (TJ‐23), affect airway smooth muscle tone and, if so, to determine what the mechanism of action is. Rabbit tracheal segments were isolated and the contractile responses to electrical field stimulation and acetylcholine were measured before and after the application of TJ‐17 or TJ‐23 under isometric conditions in vitro. Ouabain‐sensitive rubidium‐86 (86Rb) uptake by tissues in response to each drug was also measured. Each herbal medicine attenuated the contractile responses to electrical field stimulation and acetylcholine in a concentration‐dependent manner, the maximal inhibition of acetylcholine‐induced contraction being 37.5±4.9% for TJ‐17 and 42.4±5.3% for TJ‐23 (p&lt;0.05 for each). These effects were not altered by mechanical removal of the epithelium, indomethacin, the nitric oxide synthase inhibitor NG‐nitro‐ l‐arginine methyl ester, the cyclic adenosine monophosphate (cAMP)‐dependent protein kinase inhibitor adenosine 3′5′‐cyclic monophosphorothiioate (Rp‐cAMPS), the cyclic guanosine monophosphate (cGMP)‐dependent protein kinase inhibitor KT5823, or the calcium (Ca2+)‐activated potassium (K+) channel inhibitor chary‐bdotoxin, but were greatly inhibited in the presence of the sodium (Na+)‐K+ adenosine triphosphatase (ATPase) inhibitor ouabain. Incubation of tissues with TJ‐17 and TJ‐23 dose dependently increased ouabain‐sensitive 86Rb uptake. The results of the study suggest that both Gorei‐San and Toki‐Shakuyaku‐San reduce airway smooth muscle tone via a postjunctional mechanism probably through stimulation of the sodium pump and the subsequent hyperpolarization/repolarization of the cell membrane. 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subjects Acetylcholine
Acetylcholine - antagonists & inhibitors
Acetylcholine - pharmacology
Animals
asthma
Biological and medical sciences
Bronchial Provocation Tests
bronchoconstriction
Bronchoconstriction - drug effects
Culture Techniques
Drugs, Chinese Herbal - pharmacology
Female
Male
Medical sciences
Medicine, Kampo
Muscle, Smooth - drug effects
ouabain
Pharmacology. Drug treatments
Rabbits
Respiratory system
sodium‐potassium adenosine triphosphate
title Inhibition of airway smooth muscle tone by Chinese herbal medicines
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