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Is Senna Laxative Use Associated to Cathartic Colon, Genotoxicity, or Carcinogenicity?

Due to their natural origin, apparent low oral toxicity, effectiveness, and accessibility without a medical prescription, the anthranoid laxatives are a popular remedy for constipation and are frequently used abusively. Therefore, it is important to characterize its harmful and/or toxic effects. The...

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Detalles Bibliográficos
Autores principales: Morales, M. A., Hernández, D., Bustamante, S., Bachiller, I., Rojas, A.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809429/
https://www.ncbi.nlm.nih.gov/pubmed/20107583
http://dx.doi.org/10.1155/2009/287247
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author Morales, M. A.
Hernández, D.
Bustamante, S.
Bachiller, I.
Rojas, A.
author_facet Morales, M. A.
Hernández, D.
Bustamante, S.
Bachiller, I.
Rojas, A.
author_sort Morales, M. A.
collection PubMed
description Due to their natural origin, apparent low oral toxicity, effectiveness, and accessibility without a medical prescription, the anthranoid laxatives are a popular remedy for constipation and are frequently used abusively. Therefore, it is important to characterize its harmful and/or toxic effects. The sennosides, main active metabolites of senna, exhibit a very low toxicity in rats, and its genotoxic activity in bacterial strains as well as mammal cells was classified as weak in those cases where it was shown to be significant. The toxicological and mutagenic status of the crude extract of senna, however, is not as well characterized, and it is necessary to do so since it is frequently, and at the same time incorrectly, believed that the chronic use of anthranoid laxatives is a risk factor for the development of colorectal cancer. The objective of this article was to review the information that arises in various scientific medical databases using key words such as senna, sen, Senna alexandrina, Cassia angustifolia, sennosides, laxative toxicity, mainly ISI and non-ISI articles of journals with an editorial committee. Web pages of products or companies that publicize or commercialize this type of laxative were not included. This analysis establishes that (1) there is no convincing evidence that the chronic use of senna has, as a consequence, a structural and/or functional alteration of the enteric nerves or the smooth intestinal muscle, (2) there is no relation between long-term administration of a senna extract and the appearance of gastrointestinal tumors or any other type in rats, (3) senna is not carcinogenic in rats even after a two-year daily dose of up to 300 mg/kg/day, and (4) the current evidence does not show that there is a genotoxic risk for patients who take laxatives containing senna extracts or sennosides.
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spelling pubmed-28094292010-01-27 Is Senna Laxative Use Associated to Cathartic Colon, Genotoxicity, or Carcinogenicity? Morales, M. A. Hernández, D. Bustamante, S. Bachiller, I. Rojas, A. J Toxicol Review Article Due to their natural origin, apparent low oral toxicity, effectiveness, and accessibility without a medical prescription, the anthranoid laxatives are a popular remedy for constipation and are frequently used abusively. Therefore, it is important to characterize its harmful and/or toxic effects. The sennosides, main active metabolites of senna, exhibit a very low toxicity in rats, and its genotoxic activity in bacterial strains as well as mammal cells was classified as weak in those cases where it was shown to be significant. The toxicological and mutagenic status of the crude extract of senna, however, is not as well characterized, and it is necessary to do so since it is frequently, and at the same time incorrectly, believed that the chronic use of anthranoid laxatives is a risk factor for the development of colorectal cancer. The objective of this article was to review the information that arises in various scientific medical databases using key words such as senna, sen, Senna alexandrina, Cassia angustifolia, sennosides, laxative toxicity, mainly ISI and non-ISI articles of journals with an editorial committee. Web pages of products or companies that publicize or commercialize this type of laxative were not included. This analysis establishes that (1) there is no convincing evidence that the chronic use of senna has, as a consequence, a structural and/or functional alteration of the enteric nerves or the smooth intestinal muscle, (2) there is no relation between long-term administration of a senna extract and the appearance of gastrointestinal tumors or any other type in rats, (3) senna is not carcinogenic in rats even after a two-year daily dose of up to 300 mg/kg/day, and (4) the current evidence does not show that there is a genotoxic risk for patients who take laxatives containing senna extracts or sennosides. Hindawi Publishing Corporation 2009 2009-09-10 /pmc/articles/PMC2809429/ /pubmed/20107583 http://dx.doi.org/10.1155/2009/287247 Text en Copyright © 2009 M. A. Morales et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Morales, M. A.
Hernández, D.
Bustamante, S.
Bachiller, I.
Rojas, A.
Is Senna Laxative Use Associated to Cathartic Colon, Genotoxicity, or Carcinogenicity?
title Is Senna Laxative Use Associated to Cathartic Colon, Genotoxicity, or Carcinogenicity?
title_full Is Senna Laxative Use Associated to Cathartic Colon, Genotoxicity, or Carcinogenicity?
title_fullStr Is Senna Laxative Use Associated to Cathartic Colon, Genotoxicity, or Carcinogenicity?
title_full_unstemmed Is Senna Laxative Use Associated to Cathartic Colon, Genotoxicity, or Carcinogenicity?
title_short Is Senna Laxative Use Associated to Cathartic Colon, Genotoxicity, or Carcinogenicity?
title_sort is senna laxative use associated to cathartic colon, genotoxicity, or carcinogenicity?
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809429/
https://www.ncbi.nlm.nih.gov/pubmed/20107583
http://dx.doi.org/10.1155/2009/287247
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