Scutellaria lateriflora, (commonly "blue skullcap", "mad dog skullcap",[1][2], "American skullcap", "side-flowering skullcap", etc.) is a hardy perennial herb of the mint family, Lamiaceae, native to North America.
It has an upright habit, growing 60–80cm (24–31 inches) in maximum height.[3][4] It is a wetland-loving species and grows near marshes, meadows, and other wet habitat. The blue flowers are just under 1cm (0.4 inches) long.[3][4] Most of the flowers do not appear at the top of the main stem, but are produced along the length of side branches that grow from the leaf axils.
Traditional uses and research
Scutellaria lateriflora contains flavonoids.[5] Other skullcaps (Scutellaria species) used for similar purposes include common skullcap (S. galericulata), western skullcap (S. canescens), and southern skullcap (S. cordifolia). Its extracts are used in herbal medicine intended as a mild sedative and sleep promoter.[5] Cherokee women have used it as an emmenagogue.[6] In 1773, Scutellaria lateriflora became a common treatment in North America for the hysteria and hydrophobia caused by rabies.[7]
Skullcap products have been analyzed, with some adulterated by Teucrium canadense or T. chamaedrys, also known as germander, which contains potentially hepatotoxic diterpenes.[5]
β-Elemene in the herb is under preliminary research in vitro,[8] but studies in humans have not confirmed any efficacy.[9] Diterpenes isolated from S. barbata had cytotoxic activity against three human cancer cell lines in vitro.[10]
Pharmacology
Illustration by Charles Frederick Millspaugh
This section needs more medical references for verification or relies too heavily on primary sources. (April 2014)
Main article: Scutellaria §Constituents and pharmacology
The principal phenolics in the leaves, stems, and roots of some Scutellaria species are baicalin, baicalein, wogonin, and oroxylin A.[11][12] Baicalin has anti-inflammatory and analgesic effects in a rat model of thermal hyperalgesia.[13][14] Another study identifies 5,6,7-trihydroxy-2'- methoxyflavone and its 7-O-glucuronide.[15] A number of the flavones found in S. lateriflora have been reported to selectively bind with high affinity to central benzodiazepine receptor sites, leading to the view that the flavones exert anxiolytic and other benzodiazepine effects in rats.[16]
Scutellarin is a flavone found in S. lateriflora and S. barbata that has been investigated as a treatment for a variety of conditions. It is transformed by hydrolysis into scutellarein.
The flavonoids are found throughout the plant but are more concentrated in the leaves, and the concentrations are found to decrease slightly as the plant matures. The dried leaf is reported to contain about 50 milligrams of flavonoid per gram. The flavonoids are readily extracted using hot water.[14]
Joshee N, Patrick TS, Mentreddy RS, Yadav AK. 2002. Skullcap: Potential medicinal crop. In: J Janick,A Whipkey (eds). In Trends in New Crops and New Uses. ASHS Press: Alexandria, VA; 580– 586.
Peng X, etal. (2006). "Assessing the quality of RCTs on the effect of β-elemene, one ingredient of a Chinese herb, against malignant tumors". Contemporary Clinical Trials. 27 (1): 70–82. doi:10.1016/j.cct.2005.07.002. PMID16243588.
Qu GW, etal. (2010). "Two new cytotoxic ent-clerodane diterpenoids from Scutellaria barbata". Journal of Asian Natural Products Research. 12 (10): 859–64. doi:10.1080/10286020.2010.507546. PMID20924899. S2CID25504133.
Li J, Ding Y, Li XC, Ferreira D, Khan S, Smillie T, Khan IA (2009). "Scuteflorins A and B, dihydropyranocoumarins from Scutellaria lateriflora". J. Nat. Prod. 72 (6): 983–7. doi:10.1021/np900068t. PMID19555121.
Chou, Tz-Chong; Chang, Li-Ping; Li, Chi-Yuan; Wong, Chih-Shung; Yang, Shih-Ping (2003). "The Antiinflammatory and Analgesic Effects of Baicalin in Carrageenan-Evoked Thermal Hyperalgesia". Anesth Analg. 97 (6): 1724–1729. doi:10.1213/01.ane.0000087066.71572.3f. PMID14633550. S2CID24387980.
Bergeron, Chantal; Gafner, Stefan; Clausen, Edgar; Carrier, Danielle J. (2005). "Scutellaria lateriflora Using Accelerated Solvent Extraction and Supercritical Fluid Extraction versus Standard Hot Water or 70% Ethanol Extraction". J. Agric. Food Chem. 53 (8): 3076–3080. doi:10.1021/jf048408t. PMID15826062.
Analysis of Scutellaria lateriflora and its adulterant Teucrium canadense by HPLC-UV and HPLC-UV/MS, Tom's of Maine, PO Box 710, Kennebunk, ME 04043. USA.
Medina JH, etal. (1997). "Overview – Flavonoids: A new family of benzodiazepine receptor ligands". Neurochemical Research. 22 (4): 419–25. doi:10.1023/A:1027303609517. PMID9130252. S2CID22552052.
P.H. and Horhammer, L., Hager's Handbuch der Pharmazeutischen Praxis, Vols. 2-6, Springer-Verlag, Berlin, 1969-1979.
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