期刊论文详细信息
BMC Complementary and Alternative Medicine
Valeriana officinalis root extract suppresses physical stress by electric shock and psychological stress by nociceptive stimulation-evoked responses by decreasing the ratio of monoamine neurotransmitters to their metabolites
In Koo Hwang2  Yeo Sung Yoon2  Youn-Gil Kwak3  Jung Hoon Choi1  Jong Whi Kim2  Sung Min Nam2  Woosuk Kim2  Dae Young Yoo2  Hyo Young Jung2 
[1] Department of Anatomy, College of Veterinary Medicine, Kangwon National University, Chuncheon 200-701, South Korea;Department of Anatomy and Cell Biology, College of Veterinary Medicine, and Research Institute for Veterinary Science, Seoul National University, Seoul 151-742, South Korea;Central Research Center, Natural F&P Co. Ltd, Cheongwon 363-883, South Korea
关键词: Amygdala;    Hippocampus;    Norepinephrine;    Serotonin;    Psychological stress;    Physical stress;    Valeriana officinalis;   
Others  :  1085067
DOI  :  10.1186/1472-6882-14-476
 received in 2014-04-11, accepted in 2014-09-22,  发布年份 2014
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【 摘 要 】

Background

In this study, we investigate the effects of valerian root extracts (VE) on physical and psychological stress responses by utilizing a communication box.

Methods

Eight-week-old ICR mice received oral administration of VE (100 mg/kg/0.5 ml) or equal volume of distilled water in every day for 3 weeks prior to being subjected to physical or psychological stress for 3 days, which are induced by communication box developed for physical electric shock and psychological stress by nociceptive stimulation-evoked responses. The stress condition was assessed by forced swimming test and serum corticosterone levels. In addition, norepinephrine (NE), serotonin (5-HT), and their metabolites such as 3-methoxy-4-hydroxyphenylethyleneglycol sulfate (MHPG-SO4) and 5-hydroxyindoleacetic acid (5-HIAA) were measured in the hippocampus and amygdala at 1 h after final stress condition, respectively.

Results

Immobility time and corticosterone levels were significantly increased in both the physical and psychological stress groups compared to the control group. The administration of VE significantly reduced these parameters in both the physical and psychological stress groups. In addition, compared to the control group, physical and psychological stress groups showed significantly increased levels of MHPG-SO4 and 5-HIAA in the hippocampus and amygdala, respectively. The administration of VE significantly suppressed the increase of MHPG-SO4 and 5-HIAA in the two stress groups.

Conclusion

These results suggest that VE can suppress physical and psychological stress responses by modulating the changes in 5-HT and NE turnover in the hippocampus and amygdala.

【 授权许可】

   
2014 Jung et al.; licensee BioMed Central.

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【 参考文献 】
  • [1]Hadley S, Petry JJ: Valerian. Am Fam Phys 2003, 67:1755-1758.
  • [2]De Oliveria DM, Barreto G, De Andrade DV, Saraceno E, Aon-Bertolino L, Capani F, Dos Santos El Bachá R, Giraldez LD: Cytoprotective effect of Valeriana officinalis extract on an in vitro experimental model of Parkinson disease. Neurochem Res 2009, 34:215-220.
  • [3]Pereira RP, Fachinetto R, de Souza Prestes A, Wagner C, Sudati JH, Boligon AA, Athayde ML, Morsch VM, Rocha JB: Valeriana officinalis ameliorates vacuous chewing movements induced by reserpine in rats. J Neural Transm 2011, 118:1547-1557.
  • [4]Malva JO, Santos S, Macedo T: Neuroprotective properties of Valeriana officinalis extracts. Neurotox Res 2004, 6:131-140.
  • [5]Sudati JH, Fachinetto R, Pereira RP, Boligon AA, Athayde ML, Soares FA, de Vargas Barbosa NB, Rocha JB: In vitro antioxidant activity of Valeriana officinalis against different neurotoxic agents. Neurochem Res 2009, 34:1372-1379.
  • [6]Ortiz JG, Rassi N, Maldonado PM, González-Cabrera S, Ramos I: Commercial valerian interactions with [3H]flunitrazepam and [3H]MK-801 binding to rat synaptic membranes. Phytother Res 2006, 20:794-798.
  • [7]Sichardt K, Vissiennon Z, Koetter U, Brattström A, Nieber K: Modulation of postsynaptic potentials in rat cortical neurons by valerian extracts macerated with different alcohols: involvement of adenosine A1- and GABAA-receptors. Phytother Res 2007, 21:932-937.
  • [8]Del Valle-Mojica LM, Cordero-Hernández JM, González-Medina G, Ramos-Vélez I, Berríos-Cartagena N, Torres-Hernández BA, Ortíz JG: Aqueous and ethanolic Valeriana officinalis extracts change the binding of ligands to glutamate receptors. Evid Based Complement Alternat Med 2011, 2011:891819.
  • [9]Del Valle-Mojica LM, Ayala-Marín YM, Ortiz-Sanchez CM, Torres-Hernández BA, Abdalla-Mukhaimer S, Ortiz JG: Selective interactions of Valeriana officinalis extracts and valerenic acid with [H]glutamate binding to rat synaptic membranes. Evid Based Complement Alternat Med 2011, 2011:403591.
  • [10]Maren S, Quirk GJ: Neuronal signalling of fear memory. Nat Rev Neurosci 2004, 5:844-852.
  • [11]Ressler KJ, Nemeroff CB: Role of serotonergic and noradrenergic systems in the pathophysiology of depression and anxiety disorders. Depress Anxiety 2000, 12(Suppl 1):2-19.
  • [12]Nestler EJ, Barrot M, DiLeone RJ, Eisch AJ, Gold SJ, Monteggia LM: Neurobiology of depression. Neuron 2002, 34:13-25.
  • [13]Wong ML, Licinio J: From monoamines to genomic targets: a paradigm shift for drug discovery in depression. Nat Rev Drug Discov 2004, 3:136-151.
  • [14]Khan S, Michaud D, Moody TW, Anisman H, Merali Z: Effects of acute restraint stress on endogenous adrenomedullin levels. Neuroreport 1999, 10:2829-2833.
  • [15]Tanaka M, Yoshida M, Emoto H, Ishii H: Noradrenaline systems in the hypothalamus, amygdala and locus coeruleus are involved in the provocation of anxiety: basic studies. Eur J Pharmacol 2000, 405:397-406.
  • [16]Chen WW, He RR, Li YF, Li SB, Tsoi B, Kurihara H: Pharmacological studies on the anxiolytic effect of standardized Schisandra lignans extract on restraint-stressed mice. Phytomedicine 2011, 18:1144-1147.
  • [17]Wales JK: Does psychological stress cause diabetes? Diabet Med 1995, 12:109-112.
  • [18]Blumenthal JA, Babyak MA, Doraiswamy PM, Watkins L, Hoffman BM, Barbour KA, Herman S, Craighead WE, Brosse AL, Waugh R, Hinderliter A, Sherwood A: Exercise and pharmacotherapy in the treatment of major depressive disorder. Psychosom Med 2007, 69:587-596.
  • [19]Epel ES: Psychological and metabolic stress: a recipe for accelerated cellular aging? Hormones (Athens) 2009, 8:7-22.
  • [20]Bowman RE, Beck KD, Luine VN: Chronic stress effects on memory: sex differences in performance and monoaminergic activity. Horm Behav 2003, 43:48-59.
  • [21]Luine VN: Sex differences in chronic stress effects on memory in rats. Stress 2002, 5:205-216.
  • [22]Nam SM, Choi JH, Yoo DY, Kim W, Jung HY, Kim JW, Kang SY, Park J, Kim DW, Kim WJ, Yoon YS, Hwang IK: Valeriana officinalis extract and its main component, valerenic acid, ameliorate D-galactose-induced reductions in memory, cell proliferation, and neuroblast differentiation by reducing corticosterone levels and lipid peroxidation. Exp Gerontol 2013, 48:1369-1377.
  • [23]Sah SP, Mathela CS, Chopra K: Antidepressant effect of Valerianan wallichii patchouli alcohol chemotype in mice: behavioural and biochemical evidence. J Ethnopharmacol 2011, 135:197-200.
  • [24]Tang JY, Zeng YS, Chen QG, Qin YJ, Chen SJ, Zhong ZQ: Effects of Valerian on the level of 5-hydroxytryptamine, cell proliferation and neurons in cerebral hippocampus of rats with depression induced by chronic mild stress. Zhong Xi Yi Jie He Xue Bao 2008, 6:283-288.
  • [25]Ogawa M, Kuwabara H: Psychophysiology of emotion-communication of emotion. Shinshin-Igaku 1966, 6:352-357.
  • [26]Nadaoka I, Yasue M, Sami M, Kitagawa Y: Oral administration of Cimicifuga racemosa extract affects immobilization stress-induced changes in murine cerebral monoamine metabolism. Biomed Res 2012, 33:133-137.
  • [27]Rowland NE, Dunn AJ: Effect of dexfenfluramine on metabolic and neurochemical measures in restraint-stressed ob/ob mice. Physiol Behav 1995, 58:749-754.
  • [28]Endo Y, Shiraki K: Behavior and body temperature in rats following chronic foot shock or psychological stress exposure. Physiol Behav 2000, 71:263-268.
  • [29]Endo Y, Yamauchi K, Fueta Y, Irie M: Changes of body temperature and plasma corticosterone level in rats during psychological stress induced by the communication box. Med Sci Monit 2001, 7:1161-1165.
  • [30]Porsolt R, Bertin A, Jalfre M: Behavioral despair in mice: a primary screening test for antidepressants. Arch Int Pharmacodyn Ther 1977, 229:327-336.
  • [31]Petit-Demouliere B, Chenu F, Bourin M: Forced swimming test in mice: a review of antidepressant activity. Psychopharmacology (Berl) 2005, 177:245-255.
  • [32]Cancela L, Rossi S, Molina V: Effect of different restraint schedules on the immobility in the forced swim test: modulation by an opiate mechanism. Brain Res Bull 1991, 26:671-675.
  • [33]Poleszak E, Wlaz P, Kêdzierska E, Nieoczym D, Wyska E, Szymura-Oleksiak J, Fidecka S, Radziwon-Zaleska M, Nowak G: Immobility stress induces depression-like behavior in the forced swim test in mice: effect of magnesium and imipramine. Pharmacol Rep 2006, 58:746.
  • [34]Ishikawa M, Hara C, Ohdo S, Ogawa N: Plasma corticosterone response of rats with sociopsychological stress in the communication box. Physiol Behav 1992, 52:475-480.
  • [35]Hosoi J, Tanida M, Tsuchiya T: Mitigation of stress-induced suppression of contact hypersensitivity by odorant inhalation. Br J Dermatol 2001, 145:716-719.
  • [36]Henke PG, Ray A, Sullivan RM: The amygdala: emotions and gut functions. Dig Dis Sci 1991, 36:1633-1643.
  • [37]Conrad CD: Chronic stress-induced hippocampal vulnerability: the glucocorticoid vulnerability hypothesis. Rev Neurosci 2008, 19:395-411.
  • [38]Joëls M, Krugers H, Karst H: Stress-induced changes in hippocampal function. Prog Brain Res 2008, 167:3-15.
  • [39]Moore RY, Bloom FE: Central catecholamine neuron systems: anatomy and physiology of the norepinephrine and epinephrine systems. Annu Rev Neurosci 1979, 2:113-168.
  • [40]Stone EA: Stress and catecholamines. In Catecholamines and Behavior. Edited by Friedhoff AJ. New York: Plenum; 1975:31-72.
  • [41]Elsworth JD, Roth RH, Redmond DE Jr: Relative importance of 3-methoxy-4-hydroxyphenylglycol and 3,4-dihydroxyphenylglycol as norepinephrine metabolites in rat, monkey, and humans. J Neurochem 1983, 41:786-793.
  • [42]Kohno Y, Tanaka M, Nakagawa R, Toshima N, Nagasaki N: Regional distribution and production rate of 3-methoxy-4-hydroxyphenylethyleneglycol sulphate (MHPG-SO4) in rat brain. J Neurochem 1981, 36:286-289.
  • [43]Meek JL, Neff NH: The rate of formation of 3-methoxy-4-hydroxyphenylethyleneglycol sulfate in brain as an estimate of the rate of formation of norepinephrine. J Pharmacol Exp Ther 1973, 184:570-575.
  • [44]Sudha S, Pradhan N: Stress-induced changes in regional monoamine metabolism and behavior in rats. Physiol Behav 1995, 57:1061-1066.
  • [45]Baudry A, Mouillet-Richard S, Launay JM, Kellermann O: New views on antidepressant action. Curr Opin Neurobiol 2011, 21:858-865.
  • [46]Tanaka M, Tsuda A, Yokoo H, Yoshida M, Ida Y, Nishimura H: Involvement of the brain noradrenaline system in emotional changes caused by stress in rats. Ann N Y Acad Sci 1990, 597:159-174.
  • [47]Coplan JD, Gorman JM, Klein DF: Serotonin related functions in panic-anxiety: a critical overview. Neuropsychopharmacology 1992, 6:189-200.
  • [48]De Vry J: 5-HT1A receptor agonists: recent developments and controversial issues. Psychopharmacology (Berl) 1995, 121:1-26.
  • [49]Holmes A: Genetic variation in cortico-amygdala serotonin function and risk for stress-related disease. Neurosci Biobehav Rev 2008, 32:1293-1314.
  • [50]Steinbusch HW: Distribution of serotonin-immunoreactivity in the central nervous system of the rat-cell bodies and terminals. Neuroscience 1981, 6:557-618.
  • [51]Li JM, Kong LD, Wang YM, Cheng CH, Zhang WY, Tan WZ: Behavioral and biochemical studies on chronic mild stress models in rats treated with a Chinese traditional prescription Banxia-houpu decoction. Life Sci 2003, 74:55-73.
  • [52]Tõnissaar M, Herm L, Eller M, Kõiv K, Rinken A, Harro J: Rats with high or low sociability are differently affected by chronic variable stress. Neuroscience 2008, 152:867-876.
  • [53]Adell A, Garcia-Marquez C, Armario A, Gelpi E: Chronic stress increases serotonin and noradrenaline in rat brain and sensitizes their responses to a further acute stress. J Neurochem 1988, 50:1678-1681.
  • [54]Mitchell SN, Thomas PJ: Effect of restraint stress and anxiolytics on 5-HT turnover in rat brain. Pharmacology 1988, 37:105-113.
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