Liječenje površinskih rana štakora biljkom Anogeissus latifolia

Wound healing potential of etnanolic extract of Anogeissus latifolia bark (ALE) for treatment of dermal wounds in rats was studied on excision and incision wound models. HPTLC of the total extract was recorded for the purpose of standardization. Various parameters of incision wound, viz. epithelization period, scar area, tensile strength and hydroxyproline measurements along with wound contraction, were used to evaluate the effect of A. latifolia on wound healing. The results obtained indicate that A. latifolia accelerates the wound healing process by decreasing the surface area of the wound and increasing the tensile strength. Nitrofurazone ointment was used as a positive control. Complete epithelization was observed within 15 days with ALE. Measurements of the healed area and the hydroxyproline level were in agreement. Antibacterial activity of ALE was studied against Gram-positive (Staphylococcus aureus) and Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa and Klebsiella pneumoniae) compared to erythromycin and tetracycline. Moderate activity was observed against all organisms. The present study provides a scientific rationale for the traditional use of Anogeissus latifolia in the management of skin diseases such as sores, boils and itching.Ispitivan je potencijal liječenja alkoholnog ekstrakta kore biljke Anogeissus latifolia (ALE) na površinskim ranama štakora. U svrhu standardizacije snimljen je HPTLC kromatogram ekstrakta. Da bi se odredio učinak na zacjeljivanje oljeda praćeni su različiti parametri: vrijeme potrebno za epitelizaciju, površina ožiljka, sila naprezanja, kontrakcija rane i određivanje hidroksiprolina. Dobiveni rezultati ukazuju da A. latifolia ubrzava proces zacjeljivanja rana jer smanjuje površinu rane i povećava silu naprezanja. Mast nitrofurazona je upotrebljena kao pozitivna kontrola. Unutar 15 dan primjene ekstrakta zapažena je potpuna epitelizacija rane. Mjerenja zacjeljene površine i količine hidroksiprolina bila su u skladu. Antibakterijsko djelovanje ALE proučavano je na Gram-pozitivnim (Staphylococcus aureus) i Gram-negativnim bakterijama (Escherichia coli, Pseudomonas aeruginosa i Klebsiella pneumoniae) i uspoređeno s djelovanjem eritromicina i tetraciklina. Primjećeno je umjereno djelovanje protiv svih ispitivanih bakterija. Istraživanja su pokazala znanstvenu opravdanost tradicionalne primjene biljke Anogeissus latifolia u liječenju različitih bolesti kože kao što su rane, gnojni čirevi i svrbež

Sposobnost hvatanja slobodnih radikala biljke Saussarea costus

Saussurea costus (Falc.) Lipschitz belonging to the family Asteraceae is an important medicinal drug, roots of which are widely used as a folk medicine. The antioxidant activity of the plant has been studied using its ability to scavenge DPPH, nitric oxide, superoxide radicals along with the ability to inhibit lipid peroxidation and GSH oxidation. The 1 mg mL-1 extract had antioxidant activity with 85.2% reduction of DPPH and a 72.7% decrease in lipid peroxidation. It showed the maximum inhibition of superoxide radical of 66,0%, and 58.4% inhibition of the nitric oxide formation. The concentration of chlorogenic acid was found to be 0.027% in the extract of S. costus. Thus therapeutic activity of the plant may be due to its antioxidant activity, which may be as a result of chlorogenic acid presence.Saussurea costus (Falc.) Lipschitz (Asteraceae) važna je ljekovita biljka čiji se korijen upotrebljava u narodnoj medicini. U ovom radu proučavano je antioksidativno djelovanje te biljke. Praćena je sposobnost vezanja DPPH, oksida dušika, superoksidnih radikala i inhibicije peroksidacije lipida i oksidacije GSH. 1 mg mL-1 ekstrakta reducira 85,2% DPPH i za 72,7% smanjuje peroksidaciju lipida. Maksimalna inhibicija superoksidnih radikala bila je 66%, a inhibicija stvaranja oksida dušika 58,4%. Koncentracija klorogenske kiseline u ekstraktu S. costus je 0,027%. Smatra se da je upravo prisutnost te kiseline presudno za antioksidativno djelovanje

Cocos nucifera L. inflorescence extract: An effective hepatoprotective agent

128-136The flowering inflorescence of Cocos nucifera, a main constituent of several traditional drug formulations was investigated with a view to study the effect of the acetone extract of C. nucifera inflorescence (CnAE) on acetaminophen-induced hepatotoxicity. The total phenol and flavonoid contents of the extract are found to be 222.6 µg gallic acid equivalent/g and 120.8 µg quercetin equivalent/g, respectively. The LD50 value was >5000 mg/kg b.w. The antioxidant activity was assessed using three methods, namely, 2,2’- diphenyl-1-picryl hydrazyl assay, 2,2’-azinobis (3-ethylbenzthiazoline-6-sulphonic acid) assay and ferric reducing antioxidant power assay and the IC50 values were found to be 65.72, 66.94 and 89.84 μg/mL, respectively. Effect of CnAE (100, 200 and 400 mg/kg b.w.) and silymarin (100 mg/kg b.w.) against acetaminophen-induced liver toxicity was evaluated in Wistar rats. The study showed that CnAE pre-treated groups remarkably prevented the increase in serum alanine amino transferase, aspartate amino transferase and alkaline phosphatase level and decrease in the level of liver superoxide dismutase, reduced glutathione, glutathione-S-transferase and glutathione peroxidise. The extract also suppressed the elevated level of malondialdehyde. The biochemical determinations supported the histopathological examination and blood parameter findings. The findings of our study indicated that the phenolic-rich CnAE could be an interesting alternative candidate against acetaminophen-induced hepato-toxicity and associated oxidative stress

Cocos nucifera L. inflorescence extract: An effective hepatoprotective agent

The flowering inflorescence of Cocos nucifera, a main constituent of several traditional drug formulations was investigated with a view to study the effect of the acetone extract of C. nucifera inflorescence (CnAE) on acetaminophen-induced hepatotoxicity. The total phenol and flavonoid contents of the extract are found to be 222.6 µg gallic acid equivalent/g and 120.8 µg quercetin equivalent/g, respectively. The LD50 value was >5000 mg/kg b.w. The antioxidant activity was assessed using three methods, namely, 2,2’- diphenyl-1-picryl hydrazyl assay, 2,2’-azinobis (3-ethylbenzthiazoline-6-sulphonic acid) assay and ferric reducing antioxidant power assay and the IC50 values were found to be 65.72, 66.94 and 89.84 μg/mL, respectively. Effect of CnAE (100, 200 and 400 mg/kg b.w.) and silymarin (100 mg/kg b.w.) against acetaminophen-induced liver toxicity was evaluated in Wistar rats. The study showed that CnAE pre-treated groups remarkably prevented the increase in serum alanine amino transferase, aspartate amino transferase and alkaline phosphatase level and decrease in the level of liver superoxide dismutase, reduced glutathione, glutathione-S-transferase and glutathione peroxidise. The extract also suppressed the elevated level of malondialdehyde. The biochemical determinations supported the histopathological examination and blood parameter findings. The findings of our study indicated that the phenolic-rich CnAE could be an interesting alternative candidate against acetaminophen-induced hepato-toxicity and associated oxidative stress

The genus Spilanthes ethnopharmacology, phytochemistry, and pharmacological properties: a review

Spilanthes spp. are popular, over-the-counter remedies; they are sold over the internet under various names and are widely used in traditional medicine in various cultures. This review will summarize the important reports on the ethnopharmacology, botany, phytochemistry, and pharmacological properties as described in the literature from recent years (1920 to 2013). Spilanthes spp. are used for more than 60 types of disorders. They are reported to contain a number of biologically active phytochemicals, although a large number of ethnopharmacological uses have been documented; only a few of these species have been investigated for their chemical and biological activities. The studies are carried out mainly on Spilanthes extracts and a few metabolites substantiate the uses of these plants in traditional medicine. Well-conducted pharmacological studies are still needed for several traditional indications, and the mechanisms of action by which the plant extracts and the active compounds exert their pharmacological effects remain to be studied. They are predominantly used as extracts in personal care products, traditional medicines, and the pharmaceutical and culinary areas. Suggestions are made regarding some of the possible mechanisms of action as to how the known compounds may exert their biological activity

The Genus Spilanthes Ethnopharmacology, Phytochemistry, and Pharmacological Properties: A Review

Spilanthes spp. are popular, over-the-counter remedies; they are sold over the internet under various names and are widely used in traditional medicine in various cultures. This review will summarize the important reports on the ethnopharmacology, botany, phytochemistry, and pharmacological properties as described in the literature from recent years (1920 to 2013). Spilanthes spp. are used for more than 60 types of disorders. They are reported to contain a number of biologically active phytochemicals, although a large number of ethnopharmacological uses have been documented; only a few of these species have been investigated for their chemical and biological activities. The studies are carried out mainly on Spilanthes extracts and a few metabolites substantiate the uses of these plants in traditional medicine. Well-conducted pharmacological studies are still needed for several traditional indications, and the mechanisms of action by which the plant extracts and the active compounds exert their pharmacological effects remain to be studied. They are predominantly used as extracts in personal care products, traditional medicines, and the pharmaceutical and culinary areas. Suggestions are made regarding some of the possible mechanisms of action as to how the known compounds may exert their biological activity

Exploring the Protective Effects of Abrus precatorius in HepG2 and N-Nitrosodiethylamine-Induced Hepatocellular Carcinoma in Swiss Albino Rats: Protective effect of Abrus procatorius against hepatoarcinoma

This study was designed to explore the protective effects of Abrus precatorius L. (Leguminosae) (AP) in HepG2 cells and N-nitrosodiethylamine (NDEA) induced hepatocellular carcinoma in Swiss albino rats. The effects of aqueous/ethanolic (50%) extract of AP on hepatic markers, haematological and histopathological parameters, and antioxidant enzymes were evaluated in NDEA (200 mg/kg and CCl4, 3 ml/kgbody weight) induced experimental hepatocarcinogenesis in Swiss albino rats. In addition, cytotoxicity of the extract and its effect on the expression on p53 were studied in human hepatoma cell line (HepG2). Results obtained from cytotoxicity studies showed that the AP extract has strong cytotoxic effects on HepG2 cells. The expression of p53 was markedly increased and maintained at high level from 6-12 hr with 100 μg/ml of AP extract. A decrease in the mean and relative liver weights in AP extract treated group at a dose of 100 and 200 mg/kg was observed compared to the control group. It was also demonstrated that AP extract provided significant protection against hepatic lipid peroxidation and increased antioxidant enzymes’ activities such as superoxide dismutase, catalase, glutathione peroxidase, glutathione S-transferase and reduced glutathione levels. In a dose-dependent manner, the AP extract reduced the NDEA-induced elevated levels of various hepatic markers such as serum glutamate pyruvate transaminase, serum glutamate oxaloacetate transaminase, alkaline phosphatase, total bilirubin and gamma glutamate transpeptidase. The haematological paremater viz. RBC, WBC and haemaglobin was restored upon treatment with AP extract at 100 and 200 mg/kg. Histopathology of the liver was also carried out to mark the pathological changes in groups under study. The results of these studies demonstrate the protective effect of AP extract against NDEA induced hepatocarcinogenesis in Swiss albino rats and in HepG2 cell