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Cyclohexylamine, an active compound from Toddalia asiatica, contracts epididymal vas deferens via serotonergic receptors
BACKGROUND: Toddalia asiatica of Rutaceae, a Taiwan folk medicine, is used as an analgesic and anti-inflammatory herb. Cyclohexylamine (CHA) is an active compound from T. asiatica. Previous reports indicate CHA contracts rat vas deferens. However, the contractile mechanism of CHA on rat vas deferens...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
China Medical University
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608847/ https://www.ncbi.nlm.nih.gov/pubmed/33854916 http://dx.doi.org/10.37796/2211-8039.1025 |
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author | Chen, Yuh-Fung Wang, Yu-Wen Chen, Ih-Sheng Tsai, Huei-Yann |
author_facet | Chen, Yuh-Fung Wang, Yu-Wen Chen, Ih-Sheng Tsai, Huei-Yann |
author_sort | Chen, Yuh-Fung |
collection | PubMed |
description | BACKGROUND: Toddalia asiatica of Rutaceae, a Taiwan folk medicine, is used as an analgesic and anti-inflammatory herb. Cyclohexylamine (CHA) is an active compound from T. asiatica. Previous reports indicate CHA contracts rat vas deferens. However, the contractile mechanism of CHA on rat vas deferens was not yet reported. The purpose of this study was to investigate the contractile mechanism of CHA on rat epididymal portion of vas deferens. METHODS: Male S.D. rats weighting between 200 g to 250 g were used. The epididymal portion of vas deferens was isolated and was added with various concentrations of serotonin, serotonin antagonists and CHA. RESULTS: Serotonin elicited dose-dependent (1 × 10(−7)M~1 × 10(−4)M) contractions on rat epididymal vas deferens, which were inhibited by pretreatment with ketanserin (1 × 10(−8) M ~ 1 × 10(−6) M), methysergide (1 × 10(−5) M) and propranolol (1 × 10(−4) M), respectively. CHA elicited dose-dependent (1 × 10(−8)M~1 × 10(−4)M) contractions on rat epididymal vas deferens. The contractions of CHA (1 × 10(−4)M) on epididymal vas deferens were enhanced by serotonin in a dose-dependent manner. Methysergide (1 × 10(−7) ~1 × 10(−5) M) did not affect the contractions evoked by CHA. However, the CHA elicited contraction was almost completely inhibited by ketanserin (1 × 10(−5) M) and was enhanced by propranolol. The effect of propranolol at the concentration of 1 × 10(−4) M on CHA was likely as CHA at high concentration alone. CONCLUSIONS: From the above results, the contraction evoked by CHA on the isolated rat epididymal vas deferens might be mediated by serotonergic receptors through 5-HT(2A) subtype. |
format | Online Article Text |
id | pubmed-7608847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | China Medical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-76088472020-12-09 Cyclohexylamine, an active compound from Toddalia asiatica, contracts epididymal vas deferens via serotonergic receptors Chen, Yuh-Fung Wang, Yu-Wen Chen, Ih-Sheng Tsai, Huei-Yann Biomedicine (Taipei) Original Article BACKGROUND: Toddalia asiatica of Rutaceae, a Taiwan folk medicine, is used as an analgesic and anti-inflammatory herb. Cyclohexylamine (CHA) is an active compound from T. asiatica. Previous reports indicate CHA contracts rat vas deferens. However, the contractile mechanism of CHA on rat vas deferens was not yet reported. The purpose of this study was to investigate the contractile mechanism of CHA on rat epididymal portion of vas deferens. METHODS: Male S.D. rats weighting between 200 g to 250 g were used. The epididymal portion of vas deferens was isolated and was added with various concentrations of serotonin, serotonin antagonists and CHA. RESULTS: Serotonin elicited dose-dependent (1 × 10(−7)M~1 × 10(−4)M) contractions on rat epididymal vas deferens, which were inhibited by pretreatment with ketanserin (1 × 10(−8) M ~ 1 × 10(−6) M), methysergide (1 × 10(−5) M) and propranolol (1 × 10(−4) M), respectively. CHA elicited dose-dependent (1 × 10(−8)M~1 × 10(−4)M) contractions on rat epididymal vas deferens. The contractions of CHA (1 × 10(−4)M) on epididymal vas deferens were enhanced by serotonin in a dose-dependent manner. Methysergide (1 × 10(−7) ~1 × 10(−5) M) did not affect the contractions evoked by CHA. However, the CHA elicited contraction was almost completely inhibited by ketanserin (1 × 10(−5) M) and was enhanced by propranolol. The effect of propranolol at the concentration of 1 × 10(−4) M on CHA was likely as CHA at high concentration alone. CONCLUSIONS: From the above results, the contraction evoked by CHA on the isolated rat epididymal vas deferens might be mediated by serotonergic receptors through 5-HT(2A) subtype. China Medical University 2020-06-05 /pmc/articles/PMC7608847/ /pubmed/33854916 http://dx.doi.org/10.37796/2211-8039.1025 Text en © the Author(s) This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Article Chen, Yuh-Fung Wang, Yu-Wen Chen, Ih-Sheng Tsai, Huei-Yann Cyclohexylamine, an active compound from Toddalia asiatica, contracts epididymal vas deferens via serotonergic receptors |
title | Cyclohexylamine, an active compound from Toddalia asiatica, contracts epididymal vas deferens via serotonergic receptors |
title_full | Cyclohexylamine, an active compound from Toddalia asiatica, contracts epididymal vas deferens via serotonergic receptors |
title_fullStr | Cyclohexylamine, an active compound from Toddalia asiatica, contracts epididymal vas deferens via serotonergic receptors |
title_full_unstemmed | Cyclohexylamine, an active compound from Toddalia asiatica, contracts epididymal vas deferens via serotonergic receptors |
title_short | Cyclohexylamine, an active compound from Toddalia asiatica, contracts epididymal vas deferens via serotonergic receptors |
title_sort | cyclohexylamine, an active compound from toddalia asiatica, contracts epididymal vas deferens via serotonergic receptors |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608847/ https://www.ncbi.nlm.nih.gov/pubmed/33854916 http://dx.doi.org/10.37796/2211-8039.1025 |
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