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Formononetin mediates neuroprotection against cerebral ischemia/reperfusion in rats via downregulation of the Bax/Bcl-2 ratio and upregulation PI3K/Akt signaling pathway.
J Neurol Sci. 2014 Sep 15; 344(1-2):100-4.JN

Abstract

Isoflavone formononetin is a typical phytoestrogen isolated from Chinese medical herb red clover. It has been reported that estrogens have neuroprotective properties, and dietary intake of phytoestrogens could reduce stroke injury in cerebral ischemia/reperfusion (I/R) animal models. In the present research, we sought to investigate the molecular mechanisms underlying the neuroprotective effects of formononetin on I/R rats. Male Sprague-Dawley rats were subjected to a 2 h period of right middle cerebral artery occlusion (MCAO) followed by 24 h of reperfusion. Then neurological deficits and brain edema were evaluated. To provide insight into the functions of phosphatidylinositol 3-kinase (PI3K)/Akt and MAPK (mitogen-activated protein kinase) signaling pathway in formononetin-induced neuroprotection, the expression of ER-α, Bax, Bcl-2, p-Akt (phosphorylated protein kinase B), and p-ERK1/2 (phosphorylated extracellular signal-regulated kinases 1/2) was determined by qPCR or Western blot assay. Consequently, we found that formononetin has significantly reduced the infarcted volume and the brain water content, and improved the neurological deficit. Formononetin also exhibited an upregulation in ER-α and p-Akt, a downregulation in the ratio of Bax/Bcl-2. However, formononetin had little effect on p-ERK1/2 proteins expression. Taken together, formononetin has shown neuroprotective effects in cerebral I/R rats, and the molecular mechanisms may correlate with the downregulation of the Bax/Bcl-2 ratio and the activation of PI3K/Akt signaling pathway.

Authors+Show Affiliations

Department of Emergency, Western Hospital, First Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.Department of Emergency, Western Hospital, First Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.Department of Physiology, Guilin Medical University, Guilin 541004, China.Department of Emergency, Western Hospital, First Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.Department of Emergency, Western Hospital, First Affiliated Hospital of Guangxi Medical University, Nanning 530007, China. Electronic address: gxxiaozm@163.com.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

24996490

Citation

Liang, Kun, et al. "Formononetin Mediates Neuroprotection Against Cerebral Ischemia/reperfusion in Rats Via Downregulation of the Bax/Bcl-2 Ratio and Upregulation PI3K/Akt Signaling Pathway." Journal of the Neurological Sciences, vol. 344, no. 1-2, 2014, pp. 100-4.
Liang K, Ye Y, Wang Y, et al. Formononetin mediates neuroprotection against cerebral ischemia/reperfusion in rats via downregulation of the Bax/Bcl-2 ratio and upregulation PI3K/Akt signaling pathway. J Neurol Sci. 2014;344(1-2):100-4.
Liang, K., Ye, Y., Wang, Y., Zhang, J., & Li, C. (2014). Formononetin mediates neuroprotection against cerebral ischemia/reperfusion in rats via downregulation of the Bax/Bcl-2 ratio and upregulation PI3K/Akt signaling pathway. Journal of the Neurological Sciences, 344(1-2), 100-4. https://doi.org/10.1016/j.jns.2014.06.033
Liang K, et al. Formononetin Mediates Neuroprotection Against Cerebral Ischemia/reperfusion in Rats Via Downregulation of the Bax/Bcl-2 Ratio and Upregulation PI3K/Akt Signaling Pathway. J Neurol Sci. 2014 Sep 15;344(1-2):100-4. PubMed PMID: 24996490.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Formononetin mediates neuroprotection against cerebral ischemia/reperfusion in rats via downregulation of the Bax/Bcl-2 ratio and upregulation PI3K/Akt signaling pathway. AU - Liang,Kun, AU - Ye,Yu, AU - Wang,Yong, AU - Zhang,Jianfeng, AU - Li,Chaoqian, Y1 - 2014/06/22/ PY - 2014/05/13/received PY - 2014/06/09/revised PY - 2014/06/16/accepted PY - 2014/7/6/entrez PY - 2014/7/6/pubmed PY - 2015/5/12/medline KW - Bax KW - Bcl-2 KW - Cerebral ischemia/reperfusion KW - ER-α KW - Formononetin KW - PI3K/Akt pathway SP - 100 EP - 4 JF - Journal of the neurological sciences JO - J. Neurol. Sci. VL - 344 IS - 1-2 N2 - Isoflavone formononetin is a typical phytoestrogen isolated from Chinese medical herb red clover. It has been reported that estrogens have neuroprotective properties, and dietary intake of phytoestrogens could reduce stroke injury in cerebral ischemia/reperfusion (I/R) animal models. In the present research, we sought to investigate the molecular mechanisms underlying the neuroprotective effects of formononetin on I/R rats. Male Sprague-Dawley rats were subjected to a 2 h period of right middle cerebral artery occlusion (MCAO) followed by 24 h of reperfusion. Then neurological deficits and brain edema were evaluated. To provide insight into the functions of phosphatidylinositol 3-kinase (PI3K)/Akt and MAPK (mitogen-activated protein kinase) signaling pathway in formononetin-induced neuroprotection, the expression of ER-α, Bax, Bcl-2, p-Akt (phosphorylated protein kinase B), and p-ERK1/2 (phosphorylated extracellular signal-regulated kinases 1/2) was determined by qPCR or Western blot assay. Consequently, we found that formononetin has significantly reduced the infarcted volume and the brain water content, and improved the neurological deficit. Formononetin also exhibited an upregulation in ER-α and p-Akt, a downregulation in the ratio of Bax/Bcl-2. However, formononetin had little effect on p-ERK1/2 proteins expression. Taken together, formononetin has shown neuroprotective effects in cerebral I/R rats, and the molecular mechanisms may correlate with the downregulation of the Bax/Bcl-2 ratio and the activation of PI3K/Akt signaling pathway. SN - 1878-5883 UR - https://www.unboundmedicine.com/medline/citation/24996490/Formononetin_mediates_neuroprotection_against_cerebral_ischemia/reperfusion_in_rats_via_downregulation_of_the_Bax/Bcl_2_ratio_and_upregulation_PI3K/Akt_signaling_pathway_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0022-510X(14)00403-1 DB - PRIME DP - Unbound Medicine ER -