Intracerebroventricular microinjection of kaempferol on memory retention of passive avoidance learning in rats: involvement of cholinergic mechanism(s)

References

• Shankar GM, Li S, Mehta TH, et al. Amyloid-β protein dimers isolated directly from Alzheimer's brains impair synaptic plasticity and memory. Nat Med. 2008;14:837.
   PubMed Web of Science ®Google Scholar
• Schliebs R, Arendt T. The significance of the cholinergic system in the brain during aging and in Alzheimer’s disease. J Neural Transm. 2006;113:1625–1644.
   PubMed Web of Science ®Google Scholar
• Miller AM, Frick BJ, Smith DM, et al. Network oscillatory activity driven by context memory processing is differently regulated by glutamatergic and cholinergic neurotransmission. Neurobiol Learn Mem. 2017;145:59–66.
   PubMed Web of Science ®Google Scholar
• Klinkenberg I, Blokland A. The validity of scopolamine as a pharmacological model for cognitive impairment: a review of animal behavioral studies. Neurosci Biobehav Rev. 2010;34:1307–1350.
   PubMed Web of Science ®Google Scholar
• Srinivas NR. Recent trends in preclinical drug–drug interaction studies of flavonoids—review of case studies, issues and perspectives. Phytother Res. 2015;29:1679–1691.
   PubMed Web of Science ®Google Scholar
• Nijveldt RJ, Van Nood E, Van Hoorn DE, et al. Flavonoids: a review of probable mechanisms of action and potential applications. Am J Clin Nutr. 2001;74:418–425.
   PubMed Web of Science ®Google Scholar
• Le Marchand L. Cancer preventive effects of flavonoids—a review. Biomed Pharmacother. 2002;56:296–301.
   PubMed Web of Science ®Google Scholar
• Tapas AR, Sakarkar D, Kakde R. Flavonoids as nutraceuticals: a review. Trop J Pharm Res. 2008;7:1089–1099.
   Web of Science ®Google Scholar
• Golshani Y, Zarei M, Mohammadi S. Acute/chronic pain relief: is althaea officinalis essential oil effective?. Avicenna J Neuropsychophysiol. 2015;2:e36586.
   Google Scholar
• Neveux S, Smith NK, Roche A, et al. Natural compounds as occult ototoxins? Ginkgo biloba flavonoids moderately damage lateral line hair cells. J Assoc Res Otolaryngol. 2017;18:275–289.
   PubMed Web of Science ®Google Scholar
• Zarei M, Mohammadi S, Komaki A. Antinociceptive activity of Inula britannica L. and patuletin: in vivo and possible mechanisms studies. J Ethnopharmacol. 2018;219:351–358.
   PubMed Web of Science ®Google Scholar
• JM, Calderon-Montano, Burgos-Morón E, Pérez-Guerrero C, et al. A review on the dietary flavonoid kaempferol. Mini Rev Med Chem. 2011;11:298–344.
   PubMed Web of Science ®Google Scholar
• Chen AY, Chen YC. A review of the dietary flavonoid, kaempferol on human health and cancer chemoprevention. Food Chem. 2013;138:2099–2107.
   PubMed Web of Science ®Google Scholar
• Moore W, Alkhalidy H, Zhou K, et al. Flavonol kaempferol improves glucose homeostasis via suppressing hepatic glucose production and enhancing insulin sensitivity in diabetic mice. FASEB J. 2017;31:646–652.
   Web of Science ®Google Scholar
• Zarei M, Mohammadi S, Shahidi S, et al. Effects of Sonchus asper and apigenin-7-glucoside on nociceptive behaviors in mice. J Pharm Pharmacogn Res. 2017;5:227–237.
   Web of Science ®Google Scholar
• Erfanparast A, Tamaddonfard E, Nemati S. Effects of intra-hippocampal microinjection of vitamin B12 on the orofacial pain and memory impairments induced by scopolamine and orofacial pain in rats. Physiol Behav. 2017;170:68–77.
   PubMed Web of Science ®Google Scholar
• Xiong Y-Q, Li B-H. Inhibitory action of chlorpromazine on intestinal movement in mice and its antagonistic agents. Zhongguo yao li xue bao [Acta Pharmacol Sin]. 1994;15:235–239.
   PubMed Web of Science ®Google Scholar
• Jung M, Perio A, Terranova J-P, et al. Effects of intracerebroventricular pirenzepine on muscarinic discriminations in rats. Eur J Pharmacol. 1987;139:111–116.
   PubMed Web of Science ®Google Scholar
• Stewart BR, Jenner P, Marsden CD. Assessment of the muscarinic receptor subtype involved in the mediation of pilocarpine-induced purposeless chewing behaviour. Psychopharmacology. 1989;97:228–234.
   PubMed Web of Science ®Google Scholar
• Sienkiewicz-Jarosz H, Członkowska A, Siemiatkowski M, et al. The effects of physostigmine and cholinergic receptor ligands on novelty-induced neophobia. J Neural Transm. 2000;107:1403–1412.
   PubMed Web of Science ®Google Scholar
• Eidi M, Zarrindast M-R, Eidi A, et al. Effects of histamine and cholinergic systems on memory retention of passive avoidance learning in rats. Eur J Pharmacol. 2003;465:91–96.
   PubMed Web of Science ®Google Scholar
• Paxinos G, Watson C. The rat brain in stereotaxic coordinates in stereotaxic coordinates. Amsterdam: Elsevier; 2007.
   Google Scholar
• Lashgari R, Motamedi F, Asl SZ, et al. Behavioral and electrophysiological studies of chronic oral administration of L-type calcium channel blocker verapamil on learning and memory in rats. Behav Brain Res. 2006;171:324–328.
   PubMed Web of Science ®Google Scholar
• Mohammadi S. Effects of Sonchus asper extract on diabetes-induced learning and memory impairment in rats. Adv Pharmacol Clin Trials. 2017;2:000116.
   Google Scholar
• Maher P, Akaishi T, Abe K. Flavonoid fisetin promotes ERK-dependent long-term potentiation and enhances memory. Proc Natl Acad Sci USA. 2006;103:16568–16573.
   PubMed Web of Science ®Google Scholar
• Okuyama S, Morita M, Miyoshi K, et al. 3,5,6,7,8,3′,4′-Heptamethoxyflavone, a citrus flavonoid, on protection against memory impairment and neuronal cell death in a global cerebral ischemia mouse model. Neurochem Int. 2014;70:30–38.
   PubMed Web of Science ®Google Scholar
• Mohammadi S, Oryan S, Komaki A, et al. Effects of hippocampal microinjection of irisin, an exercise-induced myokine, on spatial and passive avoidance learning and memory in male rats . Int J Pept Res Ther. 2019;25:1–11.
   Google Scholar
• Park JS, Rho HS, Kim DH, et al. Enzymatic preparation of kaempferol from green tea seed and its antioxidant activity. J Agric Food Chem. 2006;54:2951–2956.
   PubMed Web of Science ®Google Scholar
• Leung H-C, Lin C-J, Hour M-J, et al. Kaempferol induces apoptosis in human lung non-small carcinoma cells accompanied by an induction of antioxidant enzymes. Food Chem Toxicol. 2007;45:2005–2013.
   PubMed Web of Science ®Google Scholar
• Masella R, Di Benedetto R, Varì R, et al. Novel mechanisms of natural antioxidant compounds in biological systems: involvement of glutathione and glutathione-related enzymes. J Nutr Biochem. 2005;16:577–586.
   PubMed Web of Science ®Google Scholar
• Cos P, Calomme M, Sindambiwe J-B, et al. Cytotoxicity and lipid peroxidation-inhibiting activity of flavonoids. Planta Med. 2001;67:515–519.
   PubMed Web of Science ®Google Scholar
• Mohammadi S, Golshani Y. Neuroprotective effects of rhamnazin as a flavonoid on chronic stress-induced cognitive impairment. J Adv Neurosci Res. 2017;4:30–37.
   Google Scholar
• Spencer JP. The impact of flavonoids on memory: physiological and molecular considerations. Chem Soc Rev. 2009;38:1152–1161.
   PubMed Web of Science ®Google Scholar
• Rendeiro C, Vauzour D, Rattray M, et al. Dietary levels of pure flavonoids improve spatial memory performance and increase hippocampal brain-derived neurotrophic factor. PLoS One. 2013;8:e63535.
   PubMed Web of Science ®Google Scholar
• Rendeiro C, Guerreiro JD, Williams CM, et al. Flavonoids as modulators of memory and learning: molecular interactions resulting in behavioural effects. Proc Nutr Soc. 2012;71:246–262.
   PubMed Web of Science ®Google Scholar
• Van Can M, Tran AH, Pham DM, et al. Willughbeia cochinchinensis prevents scopolamine-induced deficits in memory, spatial learning, and object recognition in rodents. J Ethnopharmacol. 2018;214:99–105.
   PubMed Web of Science ®Google Scholar
• Sheng G, Zhang J, Gao S, et al. SKF83959 has protective effects in the scopolamine model of dementia. Biol Pharm Bull. 2018;41:427–434.
   PubMed Web of Science ®Google Scholar
• Lee JC, Kim IH, Cho JH, et al. Vanillin improves scopolamine-induced memory impairment through restoration of ID1 expression in the mouse hippocampus. Mol Med Rep. 2018;
   Web of Science ®Google Scholar
• Dennis SH, Pasqui F, Colvin EM, et al. Activation of muscarinic M1 acetylcholine receptors induces long-term potentiation in the hippocampus. Cereb Cortex. 2016;26:414–426.
   PubMed Web of Science ®Google Scholar
• Flynn DD, Ferrari‐DiLeo G, Mash DC, et al. Differential regulation of molecular subtypes of muscarinic receptors in Alzheimer's disease. J Neurochem. 2002;64:1888–1891.
   Google Scholar
• Nilsson L, Nordberg A, Hardy J, et al. Physostigmine restores 3H-acetylcholine efflux from Alzheimer brain slices to normal level. J Neural Transm. 1986;67:275–285.
   PubMed Web of Science ®Google Scholar
• Matsuoka N, Maeda N, Ohkubo Y, et al. Differential effects of physostigmine and pilocarpine on the spatial memory deficits produced by two septo-hippocampal deafferentations in rats. Brain Res. 1991;559:233–240.
   PubMed Web of Science ®Google Scholar
• Winkler J, Suhr S, Gage F, et al. Essential role of neocortical acetylcholine in spatial memory. Nature. 1995;375:484.
   PubMed Web of Science ®Google Scholar