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The herbal preparation STW 5 (Iberogast) desensitizes intestinal afferents in the rat small intestine
Visceral hypersensitivity in the upper gastrointestinal tract is a potential pathomechanism of functional dyspepsia. The herbal preparation STW 5 (Iberogast) provides symptomatic relief for this condition. We aimed to investigate whether STW 5 modulates intestinal afferent sensitivity. The herbal pr...
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Published in: | Neurogastroenterology and motility 2004-12, Vol.16 (6), p.759-764 |
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creator | Liu, C-Y Müller, M H Glatzle, J Weiser, D Kelber, O Enck, P Grundy, D Kreis, M E |
description | Visceral hypersensitivity in the upper gastrointestinal tract is a potential pathomechanism of functional dyspepsia. The herbal preparation STW 5 (Iberogast) provides symptomatic relief for this condition. We aimed to investigate whether STW 5 modulates intestinal afferent sensitivity.
The herbal preparation STW 5 or vehicle (30.8% ethanol) were administered orally in male Wister rats. After 2 h animals were anaesthetized and extracellular multi-unit intestinal afferent nerve recordings were secured from the neurovascular bundle of the mesentery in the proximal jejunum. Afferent discharge to ramp distension of the intestinal loop (0-60 cm H2O) and dose-response curves for i.v. bradykinin (10, 20 and 40 microg kg(-1)) and 5-HT (5, 10, 20 and 40 microg kg(-1)) were recorded.
Baseline discharge was not different between the vehicle and treatment group. Ramp distension was followed by a pressure dependent increase in afferent nerve discharge that was decreased following STW 5 pretreatment for all distending pressures reaching 147 +/- 8 impulses s(-1) (imp s(-1)) following STW 5 vs 171 +/- 5 imp s(-1) following vehicle at 60 cm H2O (mean +/- SEM; P < 0.05). A dose-dependent increase in afferent discharge was observed for 5-HT and bradykinin. Following STW 5 pretreatment, afferent discharge was reduced at all doses of 5-HT to 110 +/- 5 at the maximum dose after STW 5 and 128 +/- 3 imp s(-1) in controls (all P < 0.05). Afferent discharge to bradykinin was similarly reduced at 20 and 40 microg kg(-1) but not at 10 microg kg(-1) of bradykinin with a discharge rate of 176 +/- 7 imp s(-1) following STW 5 and 200 +/- 6 imp s(-1) in controls at 40 microg kg(-1) (P < 0.05).
The preparation STW 5 reduces intestinal afferent nerve discharge following chemical and mechanical stimuli, while baseline discharge is not affected. This effect of STW 5 on afferent sensitivity may contribute to its therapeutic relief of dyspeptic symptoms. |
doi_str_mv | 10.1111/j.1365-2982.2004.00576.x |
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The herbal preparation STW 5 or vehicle (30.8% ethanol) were administered orally in male Wister rats. After 2 h animals were anaesthetized and extracellular multi-unit intestinal afferent nerve recordings were secured from the neurovascular bundle of the mesentery in the proximal jejunum. Afferent discharge to ramp distension of the intestinal loop (0-60 cm H2O) and dose-response curves for i.v. bradykinin (10, 20 and 40 microg kg(-1)) and 5-HT (5, 10, 20 and 40 microg kg(-1)) were recorded.
Baseline discharge was not different between the vehicle and treatment group. Ramp distension was followed by a pressure dependent increase in afferent nerve discharge that was decreased following STW 5 pretreatment for all distending pressures reaching 147 +/- 8 impulses s(-1) (imp s(-1)) following STW 5 vs 171 +/- 5 imp s(-1) following vehicle at 60 cm H2O (mean +/- SEM; P < 0.05). A dose-dependent increase in afferent discharge was observed for 5-HT and bradykinin. Following STW 5 pretreatment, afferent discharge was reduced at all doses of 5-HT to 110 +/- 5 at the maximum dose after STW 5 and 128 +/- 3 imp s(-1) in controls (all P < 0.05). Afferent discharge to bradykinin was similarly reduced at 20 and 40 microg kg(-1) but not at 10 microg kg(-1) of bradykinin with a discharge rate of 176 +/- 7 imp s(-1) following STW 5 and 200 +/- 6 imp s(-1) in controls at 40 microg kg(-1) (P < 0.05).
The preparation STW 5 reduces intestinal afferent nerve discharge following chemical and mechanical stimuli, while baseline discharge is not affected. This effect of STW 5 on afferent sensitivity may contribute to its therapeutic relief of dyspeptic symptoms.</description><identifier>ISSN: 1350-1925</identifier><identifier>EISSN: 1365-2982</identifier><identifier>DOI: 10.1111/j.1365-2982.2004.00576.x</identifier><identifier>PMID: 15601426</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Intestine, Small - drug effects ; Intestine, Small - innervation ; Male ; Neurons, Afferent - drug effects ; Neurons, Afferent - physiology ; Plant Extracts - pharmacology ; Rats ; Rats, Wistar</subject><ispartof>Neurogastroenterology and motility, 2004-12, Vol.16 (6), p.759-764</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15601426$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, C-Y</creatorcontrib><creatorcontrib>Müller, M H</creatorcontrib><creatorcontrib>Glatzle, J</creatorcontrib><creatorcontrib>Weiser, D</creatorcontrib><creatorcontrib>Kelber, O</creatorcontrib><creatorcontrib>Enck, P</creatorcontrib><creatorcontrib>Grundy, D</creatorcontrib><creatorcontrib>Kreis, M E</creatorcontrib><title>The herbal preparation STW 5 (Iberogast) desensitizes intestinal afferents in the rat small intestine</title><title>Neurogastroenterology and motility</title><addtitle>Neurogastroenterol Motil</addtitle><description>Visceral hypersensitivity in the upper gastrointestinal tract is a potential pathomechanism of functional dyspepsia. The herbal preparation STW 5 (Iberogast) provides symptomatic relief for this condition. We aimed to investigate whether STW 5 modulates intestinal afferent sensitivity.
The herbal preparation STW 5 or vehicle (30.8% ethanol) were administered orally in male Wister rats. After 2 h animals were anaesthetized and extracellular multi-unit intestinal afferent nerve recordings were secured from the neurovascular bundle of the mesentery in the proximal jejunum. Afferent discharge to ramp distension of the intestinal loop (0-60 cm H2O) and dose-response curves for i.v. bradykinin (10, 20 and 40 microg kg(-1)) and 5-HT (5, 10, 20 and 40 microg kg(-1)) were recorded.
Baseline discharge was not different between the vehicle and treatment group. Ramp distension was followed by a pressure dependent increase in afferent nerve discharge that was decreased following STW 5 pretreatment for all distending pressures reaching 147 +/- 8 impulses s(-1) (imp s(-1)) following STW 5 vs 171 +/- 5 imp s(-1) following vehicle at 60 cm H2O (mean +/- SEM; P < 0.05). A dose-dependent increase in afferent discharge was observed for 5-HT and bradykinin. Following STW 5 pretreatment, afferent discharge was reduced at all doses of 5-HT to 110 +/- 5 at the maximum dose after STW 5 and 128 +/- 3 imp s(-1) in controls (all P < 0.05). Afferent discharge to bradykinin was similarly reduced at 20 and 40 microg kg(-1) but not at 10 microg kg(-1) of bradykinin with a discharge rate of 176 +/- 7 imp s(-1) following STW 5 and 200 +/- 6 imp s(-1) in controls at 40 microg kg(-1) (P < 0.05).
The preparation STW 5 reduces intestinal afferent nerve discharge following chemical and mechanical stimuli, while baseline discharge is not affected. This effect of STW 5 on afferent sensitivity may contribute to its therapeutic relief of dyspeptic symptoms.</description><subject>Animals</subject><subject>Intestine, Small - drug effects</subject><subject>Intestine, Small - innervation</subject><subject>Male</subject><subject>Neurons, Afferent - drug effects</subject><subject>Neurons, Afferent - physiology</subject><subject>Plant Extracts - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><issn>1350-1925</issn><issn>1365-2982</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLw0AQgBdRbK3-BdmT6CFx9pnsUYqPQsGDEY9h00xsSl7ubkH99aZYe3UuM8x88w0MIZRBzMa43cRMaBVxk_KYA8gYQCU6_jwi08PgeFcriJjhakLOvN8AgOZSn5IJUxqY5HpKMFsjXaMrbEMHh4N1NtR9R1-yN6ro9aJA179bH25oiR47X4f6Gz2tu4A-1N24ZasKHXZh16RhtI0G6lvbNAcKz8lJZRuPF_s8I68P99n8KVo-Py7md8to4BJClHKUzGorkjLlfGWLBJRgFXJVaJUaoySUWoBCUFqakitjU2FNkZZWMqyEmJGrX-_g-o_teDtva7_CprEd9luf64QZYGD-BZmRoIxKRvByD26LFst8cHVr3Vf-90HxAxLHdCU</recordid><startdate>200412</startdate><enddate>200412</enddate><creator>Liu, C-Y</creator><creator>Müller, M H</creator><creator>Glatzle, J</creator><creator>Weiser, D</creator><creator>Kelber, O</creator><creator>Enck, P</creator><creator>Grundy, D</creator><creator>Kreis, M E</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>200412</creationdate><title>The herbal preparation STW 5 (Iberogast) desensitizes intestinal afferents in the rat small intestine</title><author>Liu, C-Y ; Müller, M H ; Glatzle, J ; Weiser, D ; Kelber, O ; Enck, P ; Grundy, D ; Kreis, M E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p240t-82e41a6a37d822cab70531fe25b65899540d6305e05649d259a83a9b8da41ef33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Intestine, Small - drug effects</topic><topic>Intestine, Small - innervation</topic><topic>Male</topic><topic>Neurons, Afferent - drug effects</topic><topic>Neurons, Afferent - physiology</topic><topic>Plant Extracts - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, C-Y</creatorcontrib><creatorcontrib>Müller, M H</creatorcontrib><creatorcontrib>Glatzle, J</creatorcontrib><creatorcontrib>Weiser, D</creatorcontrib><creatorcontrib>Kelber, O</creatorcontrib><creatorcontrib>Enck, P</creatorcontrib><creatorcontrib>Grundy, D</creatorcontrib><creatorcontrib>Kreis, M E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neurogastroenterology and motility</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, C-Y</au><au>Müller, M H</au><au>Glatzle, J</au><au>Weiser, D</au><au>Kelber, O</au><au>Enck, P</au><au>Grundy, D</au><au>Kreis, M E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The herbal preparation STW 5 (Iberogast) desensitizes intestinal afferents in the rat small intestine</atitle><jtitle>Neurogastroenterology and motility</jtitle><addtitle>Neurogastroenterol Motil</addtitle><date>2004-12</date><risdate>2004</risdate><volume>16</volume><issue>6</issue><spage>759</spage><epage>764</epage><pages>759-764</pages><issn>1350-1925</issn><eissn>1365-2982</eissn><abstract>Visceral hypersensitivity in the upper gastrointestinal tract is a potential pathomechanism of functional dyspepsia. The herbal preparation STW 5 (Iberogast) provides symptomatic relief for this condition. We aimed to investigate whether STW 5 modulates intestinal afferent sensitivity.
The herbal preparation STW 5 or vehicle (30.8% ethanol) were administered orally in male Wister rats. After 2 h animals were anaesthetized and extracellular multi-unit intestinal afferent nerve recordings were secured from the neurovascular bundle of the mesentery in the proximal jejunum. Afferent discharge to ramp distension of the intestinal loop (0-60 cm H2O) and dose-response curves for i.v. bradykinin (10, 20 and 40 microg kg(-1)) and 5-HT (5, 10, 20 and 40 microg kg(-1)) were recorded.
Baseline discharge was not different between the vehicle and treatment group. Ramp distension was followed by a pressure dependent increase in afferent nerve discharge that was decreased following STW 5 pretreatment for all distending pressures reaching 147 +/- 8 impulses s(-1) (imp s(-1)) following STW 5 vs 171 +/- 5 imp s(-1) following vehicle at 60 cm H2O (mean +/- SEM; P < 0.05). A dose-dependent increase in afferent discharge was observed for 5-HT and bradykinin. Following STW 5 pretreatment, afferent discharge was reduced at all doses of 5-HT to 110 +/- 5 at the maximum dose after STW 5 and 128 +/- 3 imp s(-1) in controls (all P < 0.05). Afferent discharge to bradykinin was similarly reduced at 20 and 40 microg kg(-1) but not at 10 microg kg(-1) of bradykinin with a discharge rate of 176 +/- 7 imp s(-1) following STW 5 and 200 +/- 6 imp s(-1) in controls at 40 microg kg(-1) (P < 0.05).
The preparation STW 5 reduces intestinal afferent nerve discharge following chemical and mechanical stimuli, while baseline discharge is not affected. This effect of STW 5 on afferent sensitivity may contribute to its therapeutic relief of dyspeptic symptoms.</abstract><cop>England</cop><pmid>15601426</pmid><doi>10.1111/j.1365-2982.2004.00576.x</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Intestine, Small - drug effects Intestine, Small - innervation Male Neurons, Afferent - drug effects Neurons, Afferent - physiology Plant Extracts - pharmacology Rats Rats, Wistar |
title | The herbal preparation STW 5 (Iberogast) desensitizes intestinal afferents in the rat small intestine |
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