In vivo inhibition of gastric acid secretion by the aqueous extract of Scoparia dulcis L. in rodents

The freeze-dried aqueous extract (AE) from the aerial parts of Scoparia dulcis was tested for its effects on experimental gastric hypersecretion and ulcer in rodents. Administration of AE to animals with 4h pylorus ligature potently reduced the gastric secretion with ED(50)s of 195 mg/kg (rats) and 306 mg/kg (mice). The AE also inhibited the histamine- or bethanechol-stimulated gastric secretion in pylorus-ligated mice with similar potency suggesting inhibition of the proton pump. Bio-guided purification of the AE yielded a flavonoid-rich fraction (BuF), with a specific activity 4-8 times higher than the AE in the pylorus ligature model. BuF also inhibited the hydrolysis of ATP by H(+),K(+)-ATPase with an IC(50) of 500 microg/ml, indicating that the inhibition of gastric acid secretion of Scoparia dulcis is related to the inhibition of the proton pump. Furthermore, the AE inhibited the establishment of acute gastric lesions induced in rats by indomethacin (ED(50)=313 mg/kg, p.o.) and ethanol (ED(50)=490 mg/kg, p.o.). No influence of the AE on gastrointestinal transit allowed discarding a possible CNS or a cholinergic interaction in the inhibition of gastric secretion by the AE. Collectively, the present data pharmacologically validates the popular use of Scoparia dulcis in gastric disturbances.     

New antioxidant phenylethanol glycosides from Torenia concolor

Two new phenylethanol glycosides, phenylethyl-O-α-l-rhamnopyranosyl-(1 → 2)-β-d-glucopyranoside (torenoside A, 1) and 2′-O-3,4-dihydroxy-β-phenylethoxy-O-α-l-rhamnopyranosyl-(1″ → 3′)-(4′-O-caffeoyl)-β-d-glucopyranoside (torenoside B, 2), along with the 17 known compounds (3–19) were isolated from Torenia concolor. Those structures were established on the basis of spectroscopic analysis including NMR spectroscopic techniques (¹³C, ¹H, ¹H–¹H COSY, HMQC, HMBC, TOCSY, and NOESY). Moreover, phenylethanol glycosides 3–6 exhibited significant antioxidant activities in DPPH radical scavenging assay.     

Analgesic and antiinflammatory properties of Scoparia dulcis L. Extracts and glutinol in rodents

The analgesic, antiinflammatory and antipyretic activities of the water (WE) and ethanolic (EE) extracts of Scoparia dulcis L. were tested in mice and rats. Both extracts (0.5 and 1 g/kg) p.o., prolonged the sleeping time induced by pentobarbital in mice, EE being more active than WE. Injections of EE (0.5–2 mg/kg i.v.) to anaesthetized rats induced a dose-related hypertension inhibited by alpha-blocker drugs; the hypertension was not obtained after oral treatment. EE (0.25-1 g/kg p.o.) but not WE, reduced writhings induced by acetic acid in mice. Glutinol (30 mg/kg p.o.), a major triterpene obtained from EE, produced the same effect. The tail flick response of mice was not influenced by either extract. EE (0.5 and 1 g/kg) and glutinol (30 mg/kg) p.o., reduced the paw oedema and pleurisy induced by carrageenin in rats, but only EE (1 g/kg) reduced the paw oedema induced by dextran or histamine. No effect of EE was detected on chronic inflammation induced by cotton pellets and in yeast-induced hyperthermia in rats. The results indicate that the extract of S. dulcis is endowed with analgesic effects probably related to the antiinflammatory activity of the plant. Those effects are related mainly to the presence of glutinol and flavonoids, which exert their action on the early phase of the acute inflammatory process.     

Two new phenylpropanoid esters of rhamnose from Lagotis yunnanensis

Two new phenylpropanoid esters of rhamnose, lagotoside B (1) and lagotoside C (2), together with three known compounds (3–5), were isolated from Lagotis yunnanensis. The structures of 1 and 2 were elucidated by spectroscopic methods. Compounds 3–5 have been obtained from this species for the first time.     

New Tetracyclic Triterpene Glycosides from Picria fel-tarrae Lour

Abstract

Four tetracyclic triterpene glycosides picfeltarraenins VI(4), VII(5), VIII(6) and IX(7) along with three known compounds picfeltarraenins I_A, I_B and II were isolated from the water soluble part of Picria fel-tarrae. Their structures were elucidated on the basis of chemical and spectroscopic methods.     

Antinociceptive and Anti-inflammatory Activities of Seven Endemic Verbascum Species Growing in Turkey

The leaves, flowers, and whole aerial parts of Verbascum L. (Scrophulariaceae) species have been used to treat respiratory problems, eczema, and other types of inflammatory skin conditions in traditional Turkish medicine. Moreover, they have also been widely used as a folk medicine to produce a soothing and anti-inflammatory effect on the urinary tract. In order to evaluate their folkloric use, both antinociceptive and anti-inflammatory activities of seven endemic Verbascum species [V. chionophyllum Hub.-Mor., V. cilicicum Boiss., V. dudleyanum (Hub.-Mor.) Hub.-Mor., V. latisepalum Hub.-Mor., V. pycnostachyum Boiss. & Heldr., V. salviifolium Boiss., V. splendidum Boiss.] were investigated. Antinociceptive activity was investigated via p-benzoquinone–induced writhing test, and the anti-inflammatory activity was studied using carrageenan-induced hind paw edema, PGE₂-induced hind paw edema, and 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced mouse ear edema models in mice. The methanol extracts of the flowers of V. chionophyllum and V. pycnostachyum, and the aerial parts of V. latisepalum and V. salviifolium, displayed significant antinociceptive and anti-inflammatory activity at 200 mg/kg oral dose without inducing any apparent acute toxicity or gastric damage. On the other hand, extracts from the rest of the species did not show any remarkable anti-inflammatory and antinociceptive activity. Results of the current study support the continued and expanded use of these plant species employed in Turkish folk medicine.     

Five new iridoids from the whole plants of Rehmannia henryi

Five new iridoids (1-5), jiohenrins A-E, together with sixteen known compounds (6-21), were isolated from the whole plants of Rehmannia henryi. The structures of these compounds were elucidated on the basis of their spectroscopic data.

     

Phytotoxic and antimicrobial constituents of Bacopa monnieri and Holmskioldia sanguinea

The phytochemicals betulinic acid (1), wogonin (2) and oroxindin (3) isolated from the aerial parts of Bacopa monnieri and Holmskioldia sanguinea showed significant antifungal activity against the two fungi Alternaria alternata and Fusarium fusiformis. Inhibition of root growth germination of wheat seeds was observed for all three compounds which showed 100% inhibition at 10 micro g/mL. Compounds (1) and (2) showed potent inhibition of Alternaria alternata compared with oroxindin at a concentration of 4 micro g/mL, whereas compound (2) was an effective inhibitor of both fungi. The structures of the compounds were established by spectral and chemical studies.     

藏药云南兔耳草的化学成分研究(Ⅱ)

目的:提取、分离鉴定云南兔耳草的化学成分。方法:乙醇冷浸提取,氯仿、正丁醇依次萃取,硅胶柱层析分离纯化,通过理化常数和波谱分析鉴定化合物结构。结果:分离得到7个化合物,分别鉴定为artselaeroside A(1),3-羟基-5-甲氧基苯甲醇(3-hydroxy-5-m ethoxy-benzyl alcohol,2),对羟基苯乙醇(tyrosol,3),9′-顺-十八烯酸甘油酯(glycerin-9-′Z-octadecaenate,4),二十二酸甘油酯(glycerin-docosanate,5),二十四酸甘油酯(glycerin-tetracosanate,6),二十四烷酸(tetracosanoic ac id,7)。结论:以上化合物均为首次从该植物中分离得到。     

Antioxidative activity of the flower of <Emphasis Type="Italic">Torenia fournieri</Emphasis>

The edible flower of Torenia fournieri Linden ex E. Fourn was found to possess potent antioxidative activity in a rat brain homogenate model. Bioassay-guided isolation of the active compounds from a CH₂Cl₂–MeOH (1:1) extract led to the isolation of acteoside (1), luteolin-7-O-β-glucoside (2), apigenin-7-O-α-rhamnosyl-(1→6)-β-glucoside (3), and apigetrin (4).