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Long lasting preventive effects of piperlongumine and a Piper longum extract against stress triggered pathologies in mice

AIM: To compare doxycycline (DOX) such as oral efficacies of piperlongumine (PL) and a Piper longum fruits extract (PLE) as stress resistance inducers. MATERIALS AND METHODS: Efficacies of oral pretreatments with 5 mg/kg PL or PLE or of 50 mg/kg DOX for 10 consecutive days against stress resistance...

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Autores principales: Yadav, Vaishali, Chatterjee, Shyam Sunder, Majeed, Muhammed, Kumar, Vikas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGEYA 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665022/
https://www.ncbi.nlm.nih.gov/pubmed/26649232
http://dx.doi.org/10.5455/jice.20150921010411
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author Yadav, Vaishali
Chatterjee, Shyam Sunder
Majeed, Muhammed
Kumar, Vikas
author_facet Yadav, Vaishali
Chatterjee, Shyam Sunder
Majeed, Muhammed
Kumar, Vikas
author_sort Yadav, Vaishali
collection PubMed
description AIM: To compare doxycycline (DOX) such as oral efficacies of piperlongumine (PL) and a Piper longum fruits extract (PLE) as stress resistance inducers. MATERIALS AND METHODS: Efficacies of oral pretreatments with 5 mg/kg PL or PLE or of 50 mg/kg DOX for 10 consecutive days against stress resistance were compared. Mice in treated groups were subjected to a stress induced hyperthermia on the 1(st), 5(th), 7(th), and 10(th)day. Treated mice were then subjected to tail suspension test on the 11(th)day. Alteration in body weights, core temperatures, and gastric ulcers triggered by occasional exposures to foot shocks were determined. RESULTS: DOX like long-lasting protective effects of PL and PLE against gradual alterations in body weights, basal temperatures and transient hyperthermic responses triggered by foot shocks during the post-treatment days were observed. Altered responses of stressed mice in tail suspension test observed 1 day after the last foot-shock exposures and gastric ulcers and other pathologies quantified 1 day after the test were also suppressed in PL or PLE or DOX pretreated groups. CONCLUSION: PL and crude PLE are DOX like long-acting desensitizers of stress triggered co-morbidities. Reported observations add further experimental evidences justifying traditionally known medicinal uses of P. longum and other plants of the Piperaceae family, and reveal that PL is also another very long acting and orally active inducer of stress resistance. Efforts to confirm stress preventive potentials of low dose plant-derived products enriched in PL or piperine like amide alkaloids in volunteers and patients can be warranted.
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spelling pubmed-46650222015-12-08 Long lasting preventive effects of piperlongumine and a Piper longum extract against stress triggered pathologies in mice Yadav, Vaishali Chatterjee, Shyam Sunder Majeed, Muhammed Kumar, Vikas J Intercult Ethnopharmacol Original Research AIM: To compare doxycycline (DOX) such as oral efficacies of piperlongumine (PL) and a Piper longum fruits extract (PLE) as stress resistance inducers. MATERIALS AND METHODS: Efficacies of oral pretreatments with 5 mg/kg PL or PLE or of 50 mg/kg DOX for 10 consecutive days against stress resistance were compared. Mice in treated groups were subjected to a stress induced hyperthermia on the 1(st), 5(th), 7(th), and 10(th)day. Treated mice were then subjected to tail suspension test on the 11(th)day. Alteration in body weights, core temperatures, and gastric ulcers triggered by occasional exposures to foot shocks were determined. RESULTS: DOX like long-lasting protective effects of PL and PLE against gradual alterations in body weights, basal temperatures and transient hyperthermic responses triggered by foot shocks during the post-treatment days were observed. Altered responses of stressed mice in tail suspension test observed 1 day after the last foot-shock exposures and gastric ulcers and other pathologies quantified 1 day after the test were also suppressed in PL or PLE or DOX pretreated groups. CONCLUSION: PL and crude PLE are DOX like long-acting desensitizers of stress triggered co-morbidities. Reported observations add further experimental evidences justifying traditionally known medicinal uses of P. longum and other plants of the Piperaceae family, and reveal that PL is also another very long acting and orally active inducer of stress resistance. Efforts to confirm stress preventive potentials of low dose plant-derived products enriched in PL or piperine like amide alkaloids in volunteers and patients can be warranted. SAGEYA 2015-11-05 /pmc/articles/PMC4665022/ /pubmed/26649232 http://dx.doi.org/10.5455/jice.20150921010411 Text en Copyright: © SAGEYA http://creativecommons.org/licenses/by-nc/3.0 This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, noncommercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Original Research
Yadav, Vaishali
Chatterjee, Shyam Sunder
Majeed, Muhammed
Kumar, Vikas
Long lasting preventive effects of piperlongumine and a Piper longum extract against stress triggered pathologies in mice
title Long lasting preventive effects of piperlongumine and a Piper longum extract against stress triggered pathologies in mice
title_full Long lasting preventive effects of piperlongumine and a Piper longum extract against stress triggered pathologies in mice
title_fullStr Long lasting preventive effects of piperlongumine and a Piper longum extract against stress triggered pathologies in mice
title_full_unstemmed Long lasting preventive effects of piperlongumine and a Piper longum extract against stress triggered pathologies in mice
title_short Long lasting preventive effects of piperlongumine and a Piper longum extract against stress triggered pathologies in mice
title_sort long lasting preventive effects of piperlongumine and a piper longum extract against stress triggered pathologies in mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665022/
https://www.ncbi.nlm.nih.gov/pubmed/26649232
http://dx.doi.org/10.5455/jice.20150921010411
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