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Effects of chronic Δ(9)-tetrahydrocannabinol treatment on Rho/Rho-kinase signalization pathway in mouse brain
Δ(9)-Tetrahydrocannabinol (Δ(9)-THC) shows its effects by activating cannabinoid receptors which are on some tissues and neurons. Cannabinoid systems have role on cell proliferation and development of neurons. Furthermore, it is interesting that cannabinoid system and rho/rho-kinase signalization pa...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681306/ https://www.ncbi.nlm.nih.gov/pubmed/29158718 http://dx.doi.org/10.1016/j.jsps.2017.05.002 |
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author | Kaplan, Halil Mahir Pazarci, Percin |
author_facet | Kaplan, Halil Mahir Pazarci, Percin |
author_sort | Kaplan, Halil Mahir |
collection | PubMed |
description | Δ(9)-Tetrahydrocannabinol (Δ(9)-THC) shows its effects by activating cannabinoid receptors which are on some tissues and neurons. Cannabinoid systems have role on cell proliferation and development of neurons. Furthermore, it is interesting that cannabinoid system and rho/rho-kinase signalization pathway, which have important role on cell development and proliferation, may have role on neuron proliferation and development together. Thus, a study is planned to investigate rhoA and rho-kinase enzyme expressions and their activities in the brain of chronic Δ(9)-THC treated mice. One group of mice are treated with Δ(9)-THC once to see effects of acute treatment. Another group of mice are treated with Δ(9)-THC three times per day for one month. After this period, rhoA and rho-kinase enzyme expressions and their activities in mice brains are analyzed by ELISA method. Chronic administration of Δ(9)-THC decreased the expression of rhoA while acute treatment has no meaningful effect on it. Administration of Δ(9)-THC did not affect expression of rho-kinase on both chronic and acute treatment. Administration of Δ(9)-THC increased rho-kinase activity on both chronic and acute treatment, however, chronic treatment decreased its activity with respect to acute treatment. This study showed that chronic Δ(9)-THC treatment down-regulated rhoA expression and did not change the expression level of rho-kinase which is downstream effector of rhoA. However, it elevated the rho-kinase activity. Δ(9)-THC induced down-regulation of rhoA may cause elevation of cypin expression and may have benefit on cypin related diseases. Furthermore, use of rho-kinase inhibitors and Δ(9)-THC together can be useful on rho-kinase related diseases. |
format | Online Article Text |
id | pubmed-5681306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56813062017-11-20 Effects of chronic Δ(9)-tetrahydrocannabinol treatment on Rho/Rho-kinase signalization pathway in mouse brain Kaplan, Halil Mahir Pazarci, Percin Saudi Pharm J Article Δ(9)-Tetrahydrocannabinol (Δ(9)-THC) shows its effects by activating cannabinoid receptors which are on some tissues and neurons. Cannabinoid systems have role on cell proliferation and development of neurons. Furthermore, it is interesting that cannabinoid system and rho/rho-kinase signalization pathway, which have important role on cell development and proliferation, may have role on neuron proliferation and development together. Thus, a study is planned to investigate rhoA and rho-kinase enzyme expressions and their activities in the brain of chronic Δ(9)-THC treated mice. One group of mice are treated with Δ(9)-THC once to see effects of acute treatment. Another group of mice are treated with Δ(9)-THC three times per day for one month. After this period, rhoA and rho-kinase enzyme expressions and their activities in mice brains are analyzed by ELISA method. Chronic administration of Δ(9)-THC decreased the expression of rhoA while acute treatment has no meaningful effect on it. Administration of Δ(9)-THC did not affect expression of rho-kinase on both chronic and acute treatment. Administration of Δ(9)-THC increased rho-kinase activity on both chronic and acute treatment, however, chronic treatment decreased its activity with respect to acute treatment. This study showed that chronic Δ(9)-THC treatment down-regulated rhoA expression and did not change the expression level of rho-kinase which is downstream effector of rhoA. However, it elevated the rho-kinase activity. Δ(9)-THC induced down-regulation of rhoA may cause elevation of cypin expression and may have benefit on cypin related diseases. Furthermore, use of rho-kinase inhibitors and Δ(9)-THC together can be useful on rho-kinase related diseases. Elsevier 2017-11 2017-05-11 /pmc/articles/PMC5681306/ /pubmed/29158718 http://dx.doi.org/10.1016/j.jsps.2017.05.002 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Kaplan, Halil Mahir Pazarci, Percin Effects of chronic Δ(9)-tetrahydrocannabinol treatment on Rho/Rho-kinase signalization pathway in mouse brain |
title | Effects of chronic Δ(9)-tetrahydrocannabinol treatment on Rho/Rho-kinase signalization pathway in mouse brain |
title_full | Effects of chronic Δ(9)-tetrahydrocannabinol treatment on Rho/Rho-kinase signalization pathway in mouse brain |
title_fullStr | Effects of chronic Δ(9)-tetrahydrocannabinol treatment on Rho/Rho-kinase signalization pathway in mouse brain |
title_full_unstemmed | Effects of chronic Δ(9)-tetrahydrocannabinol treatment on Rho/Rho-kinase signalization pathway in mouse brain |
title_short | Effects of chronic Δ(9)-tetrahydrocannabinol treatment on Rho/Rho-kinase signalization pathway in mouse brain |
title_sort | effects of chronic δ(9)-tetrahydrocannabinol treatment on rho/rho-kinase signalization pathway in mouse brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681306/ https://www.ncbi.nlm.nih.gov/pubmed/29158718 http://dx.doi.org/10.1016/j.jsps.2017.05.002 |
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