References
- Talhouk RS, Karam C, Fostok S, El-Jouni W, Barbour EK. Anti-inflammatory bioactivities in plant extracts. J Med Food. 2007;10:1-10. https://doi.org/10.1089/jmf.2005.055
- Lee J, Bielory L. Complementary and alternative interventions in atopic dermatitis. Immunol Allergy Clin North Am. 2010;30:411-424. https://doi.org/10.1016/j.iac.2010.06.006
- Kato H, Li W, Koike M, Wang Y, Koike K. Phenolic glycosides from Agrimonia pilosa. Phytochemistry. 2010;71:1925-1929. https://doi.org/10.1016/j.phytochem.2010.08.007
- Koshiura R, Miyamoto K, Ikeya Y, Taguchi H. Antitumor activity of methanol extract from roots of Agrimonia pilosa Ledeb. Jpn J Pharmacol. 1985;38:9-16. https://doi.org/10.1254/jjp.38.9
- Miyamoto K, Kishi N, Koshiura R. Antitumor effect of agrimoniin, a tannin of Agrimonia pilosa Ledeb., on transplantable rodent tumors. Jpn J Pharmacol. 1987;43:187-195. https://doi.org/10.1254/jjp.43.187
- Li Y, Ooi LS, Wang H, But PP, Ooi VE. Antiviral activities of medicinal herbs traditionally used in southern mainland China. Phytother Res. 2004;18:718-722. https://doi.org/10.1002/ptr.1518
- Shin WJ, Lee KH, Park MH, Seong BL. Broad-spectrum antiviral effect of Agrimonia pilosa extract on influenza viruses. Microbiol Immunol. 2010;54:11-19. https://doi.org/10.1111/j.1348-0421.2009.00173.x
- Zhu L, Tan J, Wang B, He R, Liu Y, Zheng C. Antioxidant activities of aqueous extract from Agrimonia pilosa Ledeb and its fractions. Chem Biodivers. 2009;6:1716-1726. https://doi.org/10.1002/cbdv.200800248
- Yamaki M, Kashihara M, Ishiguro K, Takagi S. Antimicrobial Principles of Xian he cao (Agrimonia pilosa). Planta Med. 1989;55:169-170. https://doi.org/10.1055/s-2006-961915
- Jung CH, Zhou S, Ding GX, Kim JH, Hong MH, Shin YC, Kim GJ, Ko SG. Antihyperglycemic activity of herb extracts on streptozotocin-induced diabetic rats. Biosci Biotechnol Biochem. 2006;70:2556-2559. https://doi.org/10.1271/bbb.60238
- Jung CH, Kim JH, Park S, Kweon DH, Kim SH, Ko SG. Inhibitory effect of Agrimonia pilosa Ledeb. on inflammation by suppression of iNOS and ROS production. Immunol Invest. 2010;39:159-170. https://doi.org/10.3109/08820130903501790
- Bae H, Kim HJ, Shin M, Lee H, Yin CS, Ra J, Kim J. Inhibitory effect of Agrimoniae Herba on lipopolysaccharide-induced nitric oxide and proinflammatory cytokine production in BV2 microglial cells. Neurol Res. 2010;32 Suppl 1:53-57. https://doi.org/10.1179/016164109X12537002794002
- Hylden JL, Wilcox GL. Intrathecal morphine in mice: a new technique. Eur J Pharmacol. 1980;67:313-316. https://doi.org/10.1016/0014-2999(80)90515-4
- Hylden JL, Wilcox GL. Intrathecal substance P elicits a caudally-directed biting and scratching behavior in mice. Brain Res. 1981;217:212-215. https://doi.org/10.1016/0006-8993(81)90203-1
- D'Amour FE, Smith DL. A method for determining loss of pain sensation. J Pharmacol Exp Ther. 1941;72:74-79.
- Eddy NB, Leimbach D. Synthetic analgesics. II. Dithienylbutenyland dithienylbutylamines. J Pharmacol Exp Ther. 1953;107:385-393.
- Koster R, Anderson M, Beer EJ. Acetic acid for analgesic screening. Federal Proceeding. 1959;18:412.
- Choi SS, Han KJ, Lee JK, Lee HK, Han EJ, Kim DH, Suh HW. Antinociceptive mechanisms of orally administered decursinol in the mouse. Life Sci. 2003;73:471-485. https://doi.org/10.1016/S0024-3205(03)00311-4
- Park SH, Sim YB, Choi SM, Seo YJ, Kwon MS, Lee JK, Suh HW. Antinociceptive profiles and mechanisms of orally administered vanillin in the mice. Arch Pharm Res. 2009;32:1643-1649. https://doi.org/10.1007/s12272-009-2119-8
- Suh HW, Song DK, Son KH, Wie MB, Lee KH, Jung KY, Do JC, Kim YH. Antinociceptive mechanisms of dipsacus saponin C administered intracerebroventricularly in the mouse. Gen Pharmacol. 1996;27:1167-1172. https://doi.org/10.1016/S0306-3623(96)00052-3
- Suh HW, Song DK, Kim YH. Differential effects of adenosine receptor antagonists injected intrathecally on antinociception induced by morphine and beta-endorphin administered intracerebroventricularly in the mouse. Neuropeptides. 1997;31:339-344. https://doi.org/10.1016/S0143-4179(97)90069-X
- Suh HW, Chung KM, Kim YH, Huh SO, Song DK. Effects of histamine receptor antagonists injected intrathecally on antinociception induced by opioids administered intracerebroventricularly in the mouse. Neuropeptides. 1999;33:121-129. https://doi.org/10.1054/npep.1999.0006
- Chapman CR, Casey KL, Dubner R, Foley KM, Gracely RH, Reading AE. Pain measurement: an overview. Pain. 1985;22:1-31.
- Grumbach L. The prediction of analgesic activity in man by animal testing. In: Knighton RS, Dumke PR ed, Pain. Boston: Little Brown and Co.; 1966. 163-182 p.
- Vyklicky L. The techniques for the study of pain in animals. In: Bonica JJ, Liebeskind JC, Albe-Fessard DG ed, Advances in Pain Research and Theraphy, Vol. 3. New York: Raven Press; 1979. 727-745 p.
- Cumberbatch MJ, Herrero JF, Headley PM. Exposure of rat spinal neurones to NMDA, AMPA and kainate produces only short-term enhancements of responses to noxious and nonnoxious stimuli. Neurosci Lett. 1994;181:98-102. https://doi.org/10.1016/0304-3940(94)90569-X
- Schmauss C, Yaksh TL. In vivo studies on spinal opiate receptor systems mediating antinociception. II. Pharmacological profiles suggesting a differential association of mu, delta and kappa receptors with visceral chemical and cutaneous thermal stimuli in the rat. J Pharmacol Exp Ther. 1984;228:1-12.
- Yaksh TL. Direct evidence that spinal serotonin and noradrenaline terminals mediate the spinal antinociceptive effects of morphine in the periaqueductal gray. Brain Res. 1979;160:180-185. https://doi.org/10.1016/0006-8993(79)90616-4
- Yaksh TL. Multiple opioid receptor systems in brain and spinal cord: Part I. Eur J Anaesthesiol. 1984;1:171-199.
- Jensen TS, Yaksh TL. Spinal monoamine and opiate systems partly mediate the antinociceptive effects produced by glutamate at brainstem sites. Brain Res. 1984;321:287-297. https://doi.org/10.1016/0006-8993(84)90181-1
- Wigdor S, Wilcox GL. Central and systemic morphine-induced antinociception in mice: contribution of descending serotonergic and noradrenergic pathways. J Pharmacol Exp Ther. 1987;242:90-95.
Cited by
- Inhibition of cell proliferation and triggering of apoptosis by agrimonolide through MAP kinase (ERK and p38) pathways in human gastric cancer AGS cells vol.7, pp.11, 2012, https://doi.org/10.1039/c6fo00715e
- Tiliroside, the major component of Agrimonia pilosa Ledeb ethanol extract, inhibits MAPK/JNK/p38-mediated inflammation in lipopolysaccharide-activated RAW 264.7 macrophages vol.12, pp.1, 2012, https://doi.org/10.3892/etm.2016.3305
- The first record of Agrimonia gorovoii Rumjantsev in Korea (Rosaceae) vol.47, pp.2, 2017, https://doi.org/10.11110/kjpt.2017.47.2.132
- Anti-Nociceptive Effect and Standardization from Mixture of Agrimonia pilosa Ledeb and Salvia miltiorrhiza Bunge Extracts vol.21, pp.6, 2018, https://doi.org/10.1089/jmf.2017.4077
- Antinociceptive Effect of Single Components Isolated from Agrimonia pilosa Ledeb. Extract vol.87, pp.3, 2012, https://doi.org/10.3390/scipharm87030018
- The Anti-Inflammatory and the Antinociceptive Effects of Mixed Agrimonia pilosa Ledeb. and Salvia miltiorrhiza Bunge Extract vol.10, pp.6, 2012, https://doi.org/10.3390/plants10061234
- Promising Antiviral Activity of Agrimonia pilosa Phytochemicals against Severe Acute Respiratory Syndrome Coronavirus 2 Supported with In Vivo Mice Study vol.14, pp.12, 2012, https://doi.org/10.3390/ph14121313