RETRACTED ARTICLE: Honokiol suppresses the development of post-ischemic glucose intolerance and neuronal damage in mice
Honokiol, a constituent of Magnolia obovata , has various pharmacological effects, including protection against cerebral ischemia. However, few studies have been conducted to evaluate the possible neuroprotective effects of honokiol against cerebral ischemia. We recently reported that cerebral ische...
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Published in | Journal of natural medicines Vol. 66; no. 4; pp. 591 - 599 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Singapore
Springer Singapore
2012
Springer Nature B.V |
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Abstract | Honokiol, a constituent of
Magnolia obovata
, has various pharmacological effects, including protection against cerebral ischemia. However, few studies have been conducted to evaluate the possible neuroprotective effects of honokiol against cerebral ischemia. We recently reported that cerebral ischemic neuronal damage could be triggered by glucose intolerance that develops after the onset of ischemic stress (i.e., post-ischemic glucose intolerance). In addition, suppression of post-ischemic glucose intolerance significantly ameliorated ischemic neuronal damage. Here, we investigated the effects of honokiol on the development of post-ischemic glucose intolerance and neuronal damage. Mice were subjected to middle cerebral artery occlusion (MCAO) for 2 h. The development of post-ischemic glucose intolerance on day 1 and neuronal damage on day 3 after MCAO were significantly reduced by intraperitoneal administration of honokiol (10 mg/kg) compared with the vehicle-treated group. Honokiol did not affect serum insulin or adiponectin levels. However, honokiol significantly decreased the expression of phosphoenolpyruvate carboxykinase and increased the expression of 5′-AMP-activated protein kinase (AMPK) on day 1 after MCAO, compared with the vehicle-treated MCAO group. The results of this study suggest that honokiol could prevent post-ischemic glucose intolerance in an AMPK-dependent manner, which may be involved in the neuroprotective effects of honokiol against cerebral ischemia. |
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AbstractList | Honokiol, a constituent of Magnolia obovata, has various pharmacological effects, including protection against cerebral ischemia. However, few studies have been conducted to evaluate the possible neuroprotective effects of honokiol against cerebral ischemia. We recently reported that cerebral ischemic neuronal damage could be triggered by glucose intolerance that develops after the onset of ischemic stress (i.e., post-ischemic glucose intolerance). In addition, suppression of post-ischemic glucose intolerance significantly ameliorated ischemic neuronal damage. Here, we investigated the effects of honokiol on the development of post-ischemic glucose intolerance and neuronal damage. Mice were subjected to middle cerebral artery occlusion (MCAO) for 2 h. The development of post-ischemic glucose intolerance on day 1 and neuronal damage on day 3 after MCAO were significantly reduced by intraperitoneal administration of honokiol (10 mg/kg) compared with the vehicle-treated group. Honokiol did not affect serum insulin or adiponectin levels. However, honokiol significantly decreased the expression of phosphoenolpyruvate carboxykinase and increased the expression of 5′-AMP-activated protein kinase (AMPK) on day 1 after MCAO, compared with the vehicle-treated MCAO group. The results of this study suggest that honokiol could prevent post-ischemic glucose intolerance in an AMPK-dependent manner, which may be involved in the neuroprotective effects of honokiol against cerebral ischemia. Honokiol, a constituent of Magnolia obovata , has various pharmacological effects, including protection against cerebral ischemia. However, few studies have been conducted to evaluate the possible neuroprotective effects of honokiol against cerebral ischemia. We recently reported that cerebral ischemic neuronal damage could be triggered by glucose intolerance that develops after the onset of ischemic stress (i.e., post-ischemic glucose intolerance). In addition, suppression of post-ischemic glucose intolerance significantly ameliorated ischemic neuronal damage. Here, we investigated the effects of honokiol on the development of post-ischemic glucose intolerance and neuronal damage. Mice were subjected to middle cerebral artery occlusion (MCAO) for 2 h. The development of post-ischemic glucose intolerance on day 1 and neuronal damage on day 3 after MCAO were significantly reduced by intraperitoneal administration of honokiol (10 mg/kg) compared with the vehicle-treated group. Honokiol did not affect serum insulin or adiponectin levels. However, honokiol significantly decreased the expression of phosphoenolpyruvate carboxykinase and increased the expression of 5′-AMP-activated protein kinase (AMPK) on day 1 after MCAO, compared with the vehicle-treated MCAO group. The results of this study suggest that honokiol could prevent post-ischemic glucose intolerance in an AMPK-dependent manner, which may be involved in the neuroprotective effects of honokiol against cerebral ischemia. |
Author | Chen, Hwei-Hsien Chan, Ming-Huan Tokuyama, Shogo Nakamoto, Kazuo Fujita-Hamabe, Wakako Harada, Shinichi Kishimoto, Maya Kobayashi, Mana |
Author_xml | – sequence: 1 givenname: Shinichi surname: Harada fullname: Harada, Shinichi organization: Department of Clinical Pharmacy, School of Pharmaceutical Sciences, Kobe Gakuin University – sequence: 2 givenname: Maya surname: Kishimoto fullname: Kishimoto, Maya organization: Department of Clinical Pharmacy, School of Pharmaceutical Sciences, Kobe Gakuin University – sequence: 3 givenname: Mana surname: Kobayashi fullname: Kobayashi, Mana organization: Department of Clinical Pharmacy, School of Pharmaceutical Sciences, Kobe Gakuin University – sequence: 4 givenname: Kazuo surname: Nakamoto fullname: Nakamoto, Kazuo organization: Department of Clinical Pharmacy, School of Pharmaceutical Sciences, Kobe Gakuin University – sequence: 5 givenname: Wakako surname: Fujita-Hamabe fullname: Fujita-Hamabe, Wakako organization: Department of Clinical Pharmacy, School of Pharmaceutical Sciences, Kobe Gakuin University – sequence: 6 givenname: Hwei-Hsien surname: Chen fullname: Chen, Hwei-Hsien organization: Institute of Pharmacology and Toxicology, Tzu Chi University – sequence: 7 givenname: Ming-Huan surname: Chan fullname: Chan, Ming-Huan organization: Institute of Pharmacology and Toxicology, Tzu Chi University – sequence: 8 givenname: Shogo surname: Tokuyama fullname: Tokuyama, Shogo email: stoku@pharm.kobegakuin.ac.jp organization: Department of Clinical Pharmacy, School of Pharmaceutical Sciences, Kobe Gakuin University |
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Keywords | Honokiol Infarction Glucose intolerance Phosphoenolpyruvate carboxykinase Middle cerebral artery occlusion 5′-AMP-activated protein kinase |
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Snippet | Honokiol, a constituent of
Magnolia obovata
, has various pharmacological effects, including protection against cerebral ischemia. However, few studies have... Honokiol, a constituent of Magnolia obovata, has various pharmacological effects, including protection against cerebral ischemia. However, few studies have... |
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Title | RETRACTED ARTICLE: Honokiol suppresses the development of post-ischemic glucose intolerance and neuronal damage in mice |
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