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1.
Sci Pharm ; 69(1): 61-65, 2017 Aug 16.
Article in English | MEDLINE | ID: mdl-28813032

ABSTRACT

Seven diterpenoid alkaloids : delcosine(1), delsoline(2), gigactonine(3), lycoctonine(4), takaosamine(5), atisine(6) and hetisinone(7) have been isolated from the aerial parts of Consolida regalis subsp. paniculata var. paniculata. The presence of compounds 1,2,5,6 and 7 in this plant has not been previously reported.

2.
Phytother Res ; 27(3): 330-7, 2013 Mar.
Article in English | MEDLINE | ID: mdl-22585450

ABSTRACT

Vascular dysfunction plays a key role in the pathogenesis of diabetic vascular disease. In this study, we aimed to investigate whether chronic in vivo treatment of Crataegus microphylla (CM) extract in diabetic rats induced with streptozotocin (STZ, intraperitoneal, 65 mg/kg) preserves vascular function and to evaluate whether the reduction of inducible nitric oxide synthase (iNOS), proinflammatory cytokines, and lipid peroxidation mediates its mechanisms of action. Starting at 4 weeks of diabetes, CM extract (100 mg/kg) was administrated to diabetic rats for 4 weeks. In aortic rings, relaxation to acetylcholine and vasoreactivity to noradrenaline were impaired, whereas aortic iNOS expression and plasma tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), total nitrite-nitrate, and malondialdehite levels were increased in diabetic rats compared with controls. Chronic CM treatment significantly corrected all the above abnormalities in diabetic rats. In comparison, pretreatment of the aorta of diabetic rats with N-[3(aminomethyl) benzyl]-acetamidine, dihydrochloride (10(-5) M), a selective inhibitor of iNOS, produced a similar recovery in vascular reactivity. These results suggest that chronic in vivo treatment of CM preserves endothelium-dependent relaxation and vascular contraction in STZ-induced diabetes, possibly by reducing iNOS expression in the aorta and by decreasing plasma levels of TNF-α and IL-6 and by preventing lipid peroxidation.


Subject(s)
Diabetes Mellitus, Experimental/physiopathology , Endothelium, Vascular/drug effects , Plant Extracts/pharmacology , Vasodilator Agents/pharmacology , Animals , Aorta/drug effects , Crataegus , Diabetes Mellitus, Experimental/blood , Diabetes Mellitus, Experimental/drug therapy , Interleukin-6/blood , Lipid Peroxidation/drug effects , Male , Malondialdehyde/blood , Nitrates/blood , Nitric Oxide Synthase Type II/metabolism , Nitrites/blood , Rats , Tumor Necrosis Factor-alpha/blood , Vasodilation/drug effects
3.
Z Naturforsch C J Biosci ; 67(3-4): 103-7, 2012.
Article in English | MEDLINE | ID: mdl-22624325

ABSTRACT

From the roots of Aconitum vulparia Rchb., collected in Prüm (Germany), a new norditerpenoid alkaloid, named alexhumboldtine, has been isolated along with the known norditerpenoid alkaloids lappaconitine, anthranoyllycoctonine, lycoctonine, puberaconitine, ajacine, and septentriodine. The structure of alexhumboldtine was established on the basis of 1H, 13C, DEPT, homonuclear 1H COSY, NOESY, HSQC, and HMBC NMR studies. From the aerial parts of the plant another norditerpenoid alkaloid, aconorine, has been isolated.


Subject(s)
Aconitum/chemistry , Alkaloids/isolation & purification , Diterpenes/isolation & purification , Magnetic Resonance Spectroscopy
4.
Z Naturforsch C J Biosci ; 67(11-12): 541-4, 2012.
Article in English | MEDLINE | ID: mdl-23413746

ABSTRACT

Delphiniflexine, a new norditerpenoid alkaloid, together with the three known norditerpenoid alkaloids methyllycaconitine, ajadine, and acoseptrigenine were isolated from the aerial parts of Delphinium flexuosum. The structure of delphiniflexine was established on the basis of 1H, 13C, DEPT, homonuclear 1H COSY, NOESY, HSQC, and HMBC NMR studies.


Subject(s)
Alkaloids/isolation & purification , Delphinium/chemistry , Diterpenes/isolation & purification , Chromatography, High Pressure Liquid , Magnetic Resonance Spectroscopy
5.
Phytother Res ; 25(5): 778-83, 2011 May.
Article in English | MEDLINE | ID: mdl-21520472

ABSTRACT

As part of our continuing research on seaweeds, crude MeOH extracts of two green, three brown and six red algae collected from Marmara, Black, Aegean and Mediterranean Seas were screened. Four parasitic protozoa, i.e. Plasmodium falciparum, Trypanosoma brucei rhodesiense, T. cruzi, Leishmania donovani and the tubercle bacillus Mycobacterium tuberculosis were used as test organisms for the in vitro assays. The selective toxicity of the extracts was also determined against mammalian L6 cells. All seaweed extracts were active against T. brucei rhodesiense; the Dasya pedicellata extract was the most potent (IC(50) value 0.37 µg/mL). The same extract also weakly inhibited the growth of T. cruzi (IC(50) 62.02 µg/mL). All seaweed extracts also showed leishmanicidal activity (IC(50) values 16.76-69.98 µg/mL). The majority of the extracts also exhibited antiplasmodial potential and the most potent extracts were those from D. pedicellata (IC(50) 0.38 µg/mL), Codium bursa (IC(50) 1.38 µg/mL) and Caulerpa rasemosa (IC(50) 3.12 µg/mL). One brown and two red algal extracts showed some weak activity against Mycobacterium tuberculosis (MIC values 125-256 µg/mL). Except for the extract of Dasya pedicellata, none of the extracts displayed any cytotoxicity. This is the second study investigating the antiprotozoal activities of Turkish marine algae and identifies Dasya pedicellata, an understudied algal species, as a candidate for further studies.


Subject(s)
Anti-Bacterial Agents/pharmacology , Antiprotozoal Agents/pharmacology , Cytotoxins/pharmacology , Seaweed/chemistry , Animals , Black Sea , Cell Line , Cell Survival/drug effects , Chlorophyta/chemistry , Inhibitory Concentration 50 , Leishmania donovani/drug effects , Mediterranean Sea , Microbial Sensitivity Tests , Mycobacterium tuberculosis/drug effects , Parasitic Sensitivity Tests , Phaeophyceae/chemistry , Plasmodium falciparum/drug effects , Rats , Rhodophyta/chemistry , Trypanosoma/drug effects , Turkey
6.
Fitoterapia ; 76(2): 269-72, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15752647

ABSTRACT

From the capitula of Helichrysum compactum, the flavonoids apigenin, kaempferol, luteolin, naringenin, 3,5-dihydroxy-6,7,8-trimethoxyflavone, kaempferol-3-O-glucoside, luteolin-7-O-glucoside and luteolin-4',7-di-O-glucoside and from the leafy stems apigenin, kaempferol, luteolin, quercetin, apigenin-7-O-glucoside, luteolin-7-O-glucoside, and quercetin-3-O-glucoside were isolated. Extracts of the capitula of H. compactum show antioxidant activity by inhibition of lipid peroxidation and also show antibacterial activity.


Subject(s)
Anti-Bacterial Agents/pharmacology , Antifungal Agents/pharmacology , Antioxidants/pharmacology , Helichrysum , Phytotherapy , Plant Extracts/pharmacology , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/therapeutic use , Antifungal Agents/administration & dosage , Antifungal Agents/therapeutic use , Antioxidants/administration & dosage , Antioxidants/therapeutic use , Candida albicans/drug effects , Flavonoids/administration & dosage , Flavonoids/pharmacology , Flavonoids/therapeutic use , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Humans , Lipid Peroxidation/drug effects , Microbial Sensitivity Tests , Plant Extracts/administration & dosage , Plant Extracts/therapeutic use , Plant Leaves , Plant Stems
7.
Nat Prod Res ; 18(3): 211-3, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15143829

ABSTRACT

Crataegus microphylla C. Koch is one of the 17 species of Crataegus growing in Turkey [H.P.T. Ammon and R. Kaul (1994). Dtsch. Apoth. Ztg., 134, 2433, 2521, 2631.]. This report is part of a series on the chemical investigations of Crataegus species from Turkey. Nine flavonoids have been isolated from the leaves and flowers of C. microphylla C. Koch. The amounts of the flavonoids from the leaves and flowers of the plant were determined.


Subject(s)
Crataegus/chemistry , Flavonoids/chemistry , Flavonoids/isolation & purification , Flowers/chemistry , Plant Leaves/chemistry
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