Vitamin E reversed nicotine-induced toxic effects on bone biochemical markers in male rats

Introduction: Vitamin E is beneficial in restoring bone histomorphometric parameters in nicotine-treated rats. This study determined the effectiveness of 3 forms of vitamin E in restoring bone metabolism in nicotine-treated rats. Material and methods: Thirty-five male Sprague-Dawley rats were div...

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Main Authors: Mohamed , Norazlina, Hapidin, Hermizi, Othman , Faizah, Ahmad Shuid, Nazrun, Muhammad , Norliza, Soelaiman , Ima-Nirwana
Format: Article
Language:English
Published: 2010
Subjects:
Online Access:http://eprints.usm.my/35720/
http://eprints.usm.my/35720/1/AMS-6-15171.pdf
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author Mohamed , Norazlina
Hapidin, Hermizi
Othman , Faizah
Ahmad Shuid, Nazrun
Muhammad , Norliza
Soelaiman , Ima-Nirwana
author_facet Mohamed , Norazlina
Hapidin, Hermizi
Othman , Faizah
Ahmad Shuid, Nazrun
Muhammad , Norliza
Soelaiman , Ima-Nirwana
author_sort Mohamed , Norazlina
building USM Institutional Repository
collection Online Access
description Introduction: Vitamin E is beneficial in restoring bone histomorphometric parameters in nicotine-treated rats. This study determined the effectiveness of 3 forms of vitamin E in restoring bone metabolism in nicotine-treated rats. Material and methods: Thirty-five male Sprague-Dawley rats were divided into 5 groups: (1) control (C), (2) nicotine cessation (NC), (3) α-tocopherol (ATF), (4) tocotrienol-enhanced fraction (TEF) and (5) γ-tocotrienol (GTT). Treatment was carried out for 4 months. The control group was administered normal saline and olive oil throughout the treatment period while treatment for groups 2-5 was performed in 2 phases. In the first phase, the groups received nicotine 7 mg/kg intraperitoneally for 2 months. The following 2 months, group 2 received normal saline and olive oil while groups 3-5 received ATF, TEF or GTT, 60 mg/kg orally. Pre-treatment and post-treatment serum was collected for bone biochemical marker measurement using the ELISA method. Results: Nicotine increased serum bone-resorbing cytokines (interleukin-1 and interleukin-6) and the bone resorption marker pyridinoline (PYD) while reducing the bone formation marker osteocalcin after 2 months of nicotine treatment. The parameters failed to improve after nicotine was stopped for 2 months. Supplementation with the 3 forms of vitamin E improved the parameters, i.e. reduced the cytokines and pyridinoline as well as increased the osteocalcin. In addition, the TEF and GTT groups had a higher level of osteocalcin than the control group. Conclusions: Nicotine impaired bone metabolism and cessation of nicotine treatment did not reverse the effects. Vitamin E, especially the tocotrienols, restored bone metabolism that was impaired due to nicotine.
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spelling usm-357202017-07-20T05:05:00Z http://eprints.usm.my/35720/ Vitamin E reversed nicotine-induced toxic effects on bone biochemical markers in male rats Mohamed , Norazlina Hapidin, Hermizi Othman , Faizah Ahmad Shuid, Nazrun Muhammad , Norliza Soelaiman , Ima-Nirwana RA0421 Public health. Hygiene. Preventive Medicine Introduction: Vitamin E is beneficial in restoring bone histomorphometric parameters in nicotine-treated rats. This study determined the effectiveness of 3 forms of vitamin E in restoring bone metabolism in nicotine-treated rats. Material and methods: Thirty-five male Sprague-Dawley rats were divided into 5 groups: (1) control (C), (2) nicotine cessation (NC), (3) α-tocopherol (ATF), (4) tocotrienol-enhanced fraction (TEF) and (5) γ-tocotrienol (GTT). Treatment was carried out for 4 months. The control group was administered normal saline and olive oil throughout the treatment period while treatment for groups 2-5 was performed in 2 phases. In the first phase, the groups received nicotine 7 mg/kg intraperitoneally for 2 months. The following 2 months, group 2 received normal saline and olive oil while groups 3-5 received ATF, TEF or GTT, 60 mg/kg orally. Pre-treatment and post-treatment serum was collected for bone biochemical marker measurement using the ELISA method. Results: Nicotine increased serum bone-resorbing cytokines (interleukin-1 and interleukin-6) and the bone resorption marker pyridinoline (PYD) while reducing the bone formation marker osteocalcin after 2 months of nicotine treatment. The parameters failed to improve after nicotine was stopped for 2 months. Supplementation with the 3 forms of vitamin E improved the parameters, i.e. reduced the cytokines and pyridinoline as well as increased the osteocalcin. In addition, the TEF and GTT groups had a higher level of osteocalcin than the control group. Conclusions: Nicotine impaired bone metabolism and cessation of nicotine treatment did not reverse the effects. Vitamin E, especially the tocotrienols, restored bone metabolism that was impaired due to nicotine. 2010 Article PeerReviewed application/pdf en http://eprints.usm.my/35720/1/AMS-6-15171.pdf Mohamed , Norazlina and Hapidin, Hermizi and Othman , Faizah and Ahmad Shuid, Nazrun and Muhammad , Norliza and Soelaiman , Ima-Nirwana (2010) Vitamin E reversed nicotine-induced toxic effects on bone biochemical markers in male rats. Arch Med Sci, 6 (4). pp. 505-512.
spellingShingle RA0421 Public health. Hygiene. Preventive Medicine
Mohamed , Norazlina
Hapidin, Hermizi
Othman , Faizah
Ahmad Shuid, Nazrun
Muhammad , Norliza
Soelaiman , Ima-Nirwana
Vitamin E reversed nicotine-induced toxic effects on bone biochemical markers in male rats
title Vitamin E reversed nicotine-induced toxic effects on bone biochemical markers in male rats
title_full Vitamin E reversed nicotine-induced toxic effects on bone biochemical markers in male rats
title_fullStr Vitamin E reversed nicotine-induced toxic effects on bone biochemical markers in male rats
title_full_unstemmed Vitamin E reversed nicotine-induced toxic effects on bone biochemical markers in male rats
title_short Vitamin E reversed nicotine-induced toxic effects on bone biochemical markers in male rats
title_sort vitamin e reversed nicotine-induced toxic effects on bone biochemical markers in male rats
topic RA0421 Public health. Hygiene. Preventive Medicine
url http://eprints.usm.my/35720/
http://eprints.usm.my/35720/1/AMS-6-15171.pdf