<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Combinatorial Chemistry &amp; High Throughput Screening</journal-id><journal-title-group><journal-title xml:lang="en">Combinatorial Chemistry &amp; High Throughput Screening</journal-title><trans-title-group xml:lang="ru"><trans-title>Combinatorial Chemistry &amp; High Throughput Screening</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1386-2073</issn><issn publication-format="electronic">1875-5402</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">643759</article-id><article-id pub-id-type="doi">10.2174/1386207326666230606114448</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Chemistry</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Atorvastatin Calcium Ameliorates Cognitive Deficits Through the AMPK/Mtor Pathway in Rats with Vascular Dementia</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Li</surname><given-names>Xiuqin</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Chen</surname><given-names>Shaopeng</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Zheng</surname><given-names>Guiming</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Yang</surname><given-names>Yanyan</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>Yin</surname><given-names>Nan</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name><surname>Niu</surname><given-names>Xiaoli</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name><surname>Yao</surname><given-names>Lixia</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Lv</surname><given-names>Peiyuan</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution>Department of Neurology, Hebei Medical University</institution></aff><aff id="aff2"><institution>Department of Preventive Health, Hebei General Hospital</institution></aff><aff id="aff3"><institution>Department of Rheumatology and Immunology, Hebei General Hospital</institution></aff><aff id="aff4"><institution>Department of Gynecology, Hebei General Hospital</institution></aff><aff id="aff5"><institution>Department of Neurology, Hebei General Hospital</institution></aff><pub-date date-type="pub" iso-8601-date="2024-01-01" publication-format="electronic"><day>01</day><month>01</month><year>2024</year></pub-date><volume>27</volume><issue>1</issue><fpage>148</fpage><lpage>156</lpage><history><date date-type="received" iso-8601-date="2025-01-07"><day>07</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://rjpbr.com/1386-2073/article/view/643759">https://rjpbr.com/1386-2073/article/view/643759</self-uri><abstract xml:lang="en"><p id="idm46041443775152">Aim:In this study, the protective effects of atorvastatin calcium (AC) on nerve cells and cognitive improvement in vivo and in vitro were investigated by establishing cell models and vascular dementia (VD) rat models.</p><p id="idm46041443779152">Background:VD is a neurodegenerative disease characterized by cognitive deficits caused by chronic cerebral hypoperfusion. AC has been studied for its potential to cure VD but its efficacy and underlying mechanism are still unclear.</p><p id="idm46041443783120">Objective:The mechanism of action of AC on cognitive deficits in the early stages of VD is unclear. Here, the 2-vessel occlusion (2-VO) model in vivo and the hypoxia/reoxygenation (H/R) cell model in vitro was established to investigate the function of AC in VD.</p><p id="idm46041443788176">Methods:The spatial learning and memory abilities of rats were detected by the Morris method. The IL-6, tumour necrosis factor-α (TNF-α), malondialdehyde (MDA) and superoxide dismutase (SOD) in cell supernatant was tested by ELISA kits. After behavioural experiments, rats were anaesthetized and sacrificed, and their brains were extracted. One part was immediately fixed in 4% paraformaldehyde for H&amp;E, Nissl, and immunohistochemical analyses, and the other was stored in liquid nitrogen. All data were shown as mean ± SD. Statistical comparison between the two groups was performed by Students t-test. A two-way ANOVA test using GraphPad Prism 7 was applied for escape latency analysis and the swimming speed test. The difference was considered statistically significant at p &lt; 0.05.</p><p id="idm46041443797552">Results:AC decreased apoptosis, increased autophagy, and alleviated oxidative stress in primary hippocampal neurons. AC regulated autophagy-related proteins in vitro by western blotting. VD mice improved cognitively in the Morris water maze. Spatial probing tests showed that VD animals administered AC had considerably longer swimming times to the platform than VD rats. H&amp;E and Nissl staining showed that AC reduces neuronal damage in VD rats. Western blot and qRT-PCR indicated that AC in VD rats inhibited Bax and promoted LC3-II, Beclin-1, and Bcl-2 in the hippocampus region. AC also improves cognition via the AMPK/mTOR pathway.</p><p id="idm46041443805200">Conclusion:This study found that AC may relieve learning and memory deficits as well as neuronal damage in VD rats by changing the expression of apoptosis/autophagy-related genes and activating the AMPK/mTOR signalling pathway in neurons.</p></abstract><kwd-group xml:lang="en"><kwd>Atorvastatin calcium (AC)</kwd><kwd>vascular dementia (VD)</kwd><kwd>cognitive deficits</kwd><kwd>autophagy</kwd><kwd>apoptosis</kwd><kwd>AMPK/mTOR pathway.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Dichgans, M.; Leys, D. Vascular cognitive impairment. Circ. Res., 2017, 120(3), 573-591. doi: 10.1161/CIRCRESAHA.116.308426 PMID: 28154105</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Rincon, F.; Wright, C.B. Vascular cognitive impairment. Curr. Opin. Neurol., 2013, 26(1), 29-36. doi: 10.1097/WCO.0b013e32835c4f04</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Fortin, N.J.; Agster, K.L.; Eichenbaum, H.B. Critical role of the hippocampus in memory for sequences of events. Nat. Neurosci., 2002, 5(5), 458-462. doi: 10.1038/nn834 PMID: 11976705</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Lazarov, O.; Hollands, C. Hippocampal neurogenesis: Learning to remember. Prog. Neurobiol., 2016, 138-140, 1-18. doi: 10.1016/j.pneurobio.2015.12.006 PMID: 26855369</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Burke, M.J.C.; Nelson, L.; Slade, J.Y.; Oakley, A.E.; Khundakar, A.A.; Kalaria, R.N. Morphometry of the hippocampal microvasculature in post-stroke and age-related dementias. Neuropathol. Appl. Neurobiol., 2014, 40(3), 284-295. doi: 10.1111/nan.12085 PMID: 24003901</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Counts, S.E.; Alldred, M.J.; Che, S.; Ginsberg, S.D.; Mufson, E.J. Synaptic gene dysregulation within hippocampal CA1 pyramidal neurons in mild cognitive impairment. Neuropharmacology, 2014, 79, 172-179. doi: 10.1016/j.neuropharm.2013.10.018 PMID: 24445080</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Singh, R.K.; Prasad, D.N.; Bhardwaj, T.R. Synthesis in vitro/in vivo evaluation and in silico physicochemical study of prodrug approach for brain targeting of alkylating agent. Med. Chem. Res., 2013, 22(11), 5324-5336. doi: 10.1007/s00044-013-0537-0</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Singh, R.K.; Devi, S.; Prasad, D.N. Synthesis, physicochemical and biological evaluation of 2-amino-5-chlorobenzophenone derivatives as potent skeletal muscle relaxants. Arab. J. Chem., 2015, 8(3), 307-312. doi: 10.1016/j.arabjc.2011.11.013</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Corsini, A.; Bellosta, S.; Baetta, R.; Fumagalli, R.; Paoletti, R.; Bernini, F. New insights into the pharmacodynamic and pharmacokinetic properties of statins. Pharmacol. Ther., 1999, 84(3), 413-428. doi: 10.1016/S0163-7258(99)00045-5 PMID: 10665838</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Inoue, T.; Node, K. Statin therapy for vascular failure. Cardiovasc. Drugs Ther., 2007, 21(4), 281-295. doi: 10.1007/s10557-007-6038-y PMID: 17682928</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Zuo, Y.; Wang, Y.; Hu, H.; Cui, W. Atorvastatin protects myocardium against ischemia-reperfusion injury through inhibiting miR-199a-5p. Cell. Physiol. Biochem., 2016, 39(3), 1021-1030. doi: 10.1159/000447809 PMID: 27537066</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Yue, Y.H.; Bai, X.; Zhang, H.; Li, Y.; Hu, L.; Liu, L.; Mao, J.; Yang, X.; Dila, N. Gene polymorphisms affect the effectiveness of atorvastatin in treating ischemic stroke patients. Cell. Physiol. Biochem., 2016, 39(2), 630-638. doi: 10.1159/000445654 PMID: 27415775</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Torrandell-Haro, G.; Branigan, G.L.; Vitali, F.; Geifman, N.; Zissimopoulos, J.M.; Brinton, R.D. Statin therapy and risk of Alzheimers and age‐related neurodegenerative diseases. Alzheimers Dement. (N. Y.), 2020, 6(1), e12108. doi: 10.1002/trc2.12108 PMID: 33283039</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Schultz, B.G.; Patten, D.K.; Berlau, D.J. The role of statins in both cognitive impairment and protection against dementia: A tale of two mechanisms. Transl. Neurodegener., 2018, 7(1), 5. doi: 10.1186/s40035-018-0110-3 PMID: 29507718</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Wang, S.; Zhang, X.; Zhai, L.; Sheng, X.; Zheng, W.; Chu, H.; Zhang, G. Atorvastatin attenuates cognitive deficits and neuroinflammation induced by Aβ142 involving modulation of TLR4/TRAF6/NF-κB pathway. J. Mol. Neurosci., 2018, 64(3), 363-373. doi: 10.1007/s12031-018-1032-3 PMID: 29417448</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Zhao, L.; Chen, T.; Wang, C.; Li, G.; Zhi, W.; Yin, J.; Wan, Q.; Chen, L. Atorvastatin in improvement of cognitive impairments caused by amyloid β in mice: Involvement of inflammatory reaction. BMC Neurol., 2016, 16(1), 18. doi: 10.1186/s12883-016-0533-3 PMID: 26846170</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Sun, B.; Chen, L.; Wei, X.; Xiang, Y.; Liu, X.; Zhang, X. The Akt/GSK-3β pathway mediates flurbiprofen-induced neuroprotection against focal cerebral ischemia/reperfusion injury in rats. Biochem. Biophys. Res. Commun., 2011, 409(4), 808-813. doi: 10.1016/j.bbrc.2011.05.095 PMID: 21624354</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Jing, Z.; Shi, C.; Zhu, L.; Xiang, Y.; Chen, P.; Xiong, Z.; Li, W.; Ruan, Y.; Huang, L. Chronic cerebral hypoperfusion induces vascular plasticity and hemodynamics but also neuronal degeneration and cognitive impairment. J. Cereb. Blood Flow Metab., 2015, 35(8), 1249-1259. doi: 10.1038/jcbfm.2015.55 PMID: 25853908</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Nixon, R.A.; Yang, D.S. Autophagy and neuronal cell death in neurological disorders. Cold Spring Harb. Perspect. Biol., 2012, 4(10), a008839. doi: 10.1101/cshperspect.a008839 PMID: 22983160</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Son, J.H.; Shim, J.H.; Kim, K.H.; Ha, J.Y.; Han, J.Y. Neuronal autophagy and neurodegenerative diseases. Exp. Mol. Med., 2012, 44(2), 89-98. doi: 10.3858/emm.2012.44.2.031 PMID: 22257884</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Tung, Y.T.; Wang, B.J.; Hu, M.K.; Hsu, W.M.; Lee, H.; Huang, W.P.; Liao, Y.F. Autophagy: A double-edged sword in Alzheimers disease. J. Biosci., 2012, 37(1), 157-165. doi: 10.1007/s12038-011-9176-0 PMID: 22357213</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Xu, Z.; Wang, H.; Cui, X.; Jin, Y.; Xu, Z. Role of autophagy in myocardial reperfusion injury. Front. Biosci. (Elite Ed.), 2010, E2(3), 1147-1153. doi: 10.2741/e174 PMID: 20515786</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Yu, Y.; Feng, L.; Li, J.; Lan, X. A, L.; Lv, X.; Zhang, M.; Chen, L. The alteration of autophagy and apoptosis in the hippocampus of rats with natural aging-dependent cognitive deficits. Behav. Brain Res., 2017, 334, 155-162. doi: 10.1016/j.bbr.2017.07.003 PMID: 28688896</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Menzies, F.M.; Fleming, A.; Rubinsztein, D.C. Compromised autophagy and neurodegenerative diseases. Nat. Rev. Neurosci., 2015, 16(6), 345-357. doi: 10.1038/nrn3961 PMID: 25991442</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Mihaylova, M.M.; Shaw, R.J. The AMPK signalling pathway coordinates cell growth, autophagy and metabolism. Nat. Cell Biol., 2011, 13(9), 1016-1023. doi: 10.1038/ncb2329 PMID: 21892142</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Dhiman, A.; Sharma, R.; Singh, R.K. Target-based anticancer indole derivatives and insight into structure‒activity relationship: A mechanistic review update (20182021). Acta Pharm. Sin. B, 2022, 12(7), 3006-3027. doi: 10.1016/j.apsb.2022.03.021 PMID: 35865090</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Garza-Lombó, C.; Schroder, A.; Reyes-Reyes, E.M.; Franco, R. mTOR/AMPK signaling in the brain: Cell metabolism, proteostasis and survival. Curr. Opin. Toxicol., 2018, 8, 102-110. doi: 10.1016/j.cotox.2018.05.002 PMID: 30417160</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Cell culture basics https://www.vanderbilt.edu/viibre/CellCultureBasicsEU.pdf</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Yang, S.; Zhou, G.; Liu, H.; Zhang, B.; Li, J.; Cui, R.; Du, Y. Protective effects of p38 MAPK inhibitor SB202190 against hippocampal apoptosis and spatial learning and memory deficits in a rat model of vascular dementia. BioMed Res. Int., 2013, 2013, 1-9. doi: 10.1155/2013/215798 PMID: 24455679</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Zong, W.; Zeng, X.; Chen, S.; Chen, L.; Zhou, L.; Wang, X.; Gao, Q.; Zeng, G.; Hu, K.; Ouyang, D. Ginsenoside compound K attenuates cognitive deficits in vascular dementia rats by reducing the Aβ deposition. J. Pharmacol. Sci., 2019, 139(3), 223-230. doi: 10.1016/j.jphs.2019.01.013 PMID: 30799178</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Qian, X.; Xu, Q.; Li, G.; Bu, Y.; Sun, F.; Zhang, J. Therapeutic effect of idebenone on rats with vascular dementia via the MicroRNA-216a/RSK2/NF-κB axis. Neuropsychiatr. Dis. Treat., 2021, 17, 533-543. doi: 10.2147/NDT.S293614 PMID: 33628024</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Luca, M.; Luca, A.; Calandra, C. The role of oxidative damage in the pathogenesis and progression of alzheimers disease and vascular dementia. Oxid. Med. Cell. Longev., 2015, 2015, 1-8. doi: 10.1155/2015/504678 PMID: 26301043</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Zhang, L.; Fang, Y.; Cheng, X.; Lian, Y.; Xu, H.; Zeng, Z.; Zhu, H. TRPML1 participates in the progression of alzheimers disease by regulating the PPARγ/AMPK/Mtor signalling pathway. Cell. Physiol. Biochem., 2017, 43(6), 2446-2456. doi: 10.1159/000484449 PMID: 29131026</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Singh, R.K.; Prasad, D.N.; Bhardwaj, T.R. Design, synthesis and in vitro cytotoxicity study of benzodiazepine-mustard conjugates as potential brain anticancer agents. J. Saudi Chem. Soc., 2017, 21(Suppl. 1), S86-S93. doi: 10.1016/j.jscs.2013.10.004</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Li, X.; Xiao, H.; Lin, C.; Sun, W.; Wu, T.; Wang, J.; Chen, B.; Chen, X.; Cheng, D. Synergistic effects of liposomes encapsulating atorvastatin calcium and curcumin and targeting dysfunctional endothelial cells in reducing atherosclerosis. Int. J. Nanomedicine, 2019, 14, 649-665. doi: 10.2147/IJN.S189819 PMID: 30697048</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Wei, C.; Xu, X.; Zhu, H.; Zhang, X.; Gao, Z. Promotive role of microRNA 150 in hippocampal neurons apoptosis in vascular dementia model rats. Mol. Med. Rep., 2021, 23(4), 257. doi: 10.3892/mmr.2021.11896 PMID: 33576461</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Tian, Z.; Ji, X.; Liu, J. Neuroinflammation in vascular cognitive impairment and dementia: Current evidence, advances, and prospects. Int. J. Mol. Sci., 2022, 23(11), 6224. doi: 10.3390/ijms23116224 PMID: 35682903</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Ni, M.; Zhang, J.; Huang, L.; Liu, G.; Li, Q. A Rho-kinase inhibitor reverses learning and memory deficits in a Rat model of chronic cerebral ischemia by altering Bcl-2/Bax-NMDAR signaling in the cerebral cortex. J. Pharmacol. Sci., 2018, 138(2), 107-115. doi: 10.1016/j.jphs.2018.08.012 PMID: 30366873</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Kim, J.; Kundu, M.; Viollet, B.; Guan, K.L. AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1. Nat. Cell Biol., 2011, 13(2), 132-141. doi: 10.1038/ncb2152 PMID: 21258367</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Alers, S.; Löffler, A.S.; Wesselborg, S.; Stork, B. Role of AMPK-mTOR-Ulk1/2 in the regulation of autophagy: Cross talk, shortcuts, and feedbacks. Mol. Cell. Biol., 2012, 32(1), 2-11. doi: 10.1128/MCB.06159-11 PMID: 22025673</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Shinojima, N.; Yokoyama, T.; Kondo, Y.; Kondo, S. Roles of the Akt/mTOR/p70S6K and ERK1/2 signaling pathways in curcumin-induced autophagy. Autophagy, 2007, 3(6), 635-637. doi: 10.4161/auto.4916 PMID: 17786026</mixed-citation></ref></ref-list></back></article>
