Phenolic constituents of Pumbago zeylanica and their anti-oxidative effects / 中草药

Objective: To investigate the phenolic compounds from Plumbago zeylanica and their anti-oxidant activities. Methods :The phenolic compounds and their analogues were isolated and purified by silica gel column chromatography, semi-preparative HPLC, and HPLC. Their structures were identified by spectroscopy data. The isolated compounds were tested for anti-oxidant activity by ABTS assay. Results: Twelve phenolic compounds were obtained and identified as (±)-5,5’-dimethoxyl ariciresionl 4’-O-β-D-glucopyranoside (1), tracheloside (2), quercetin-3-O-β-D-galactoside (3), quercetin-3-O-β-D-glucopyranoside (4), quercetin (5), quercetin 3-O-α-L-rhamnoside (6), kaempferol-3-O-α-L-rhamnoside (7), apigenin-6-C-β-D-glucopyranoside (8), luteolin 6-C-β- glucopyranoside (9), polybotrin (10), 3-O-(β-D-glucopyranosyl)-1-(3’,5’-dimethoxy-4’-hydroxyphenyl)-1-propanone (11), and (2E,4E,1’R,3’S,5’R,8’S)-dihydrophaseic acid-3’-O-β-D-glucopyranoside (12). The anti-oxidant activity experiment showed that compounds 3-9 displayed significant anti-oxidative activities. Conclusion: All of the twelve phenolic compounds are isolated from this plant for the first time. The isolated flavones 3-9 displayed significant anti-oxidative activities.

Effect of Plumbago zeylanica administration on brain neurotransmitter level in Wistar albino rats.

According to WHO about 80% of the world’s population relies on traditional medicine for their primary health care. Plumbago zeylanica L. is a medicinal plant, belong to the family of Plumbaginaceae and the root of P. zeylanica contains several bioactive constituent like L-dopa, Plumbagin (naphthoquinone), droseron, chitranone, triterpenoid, anthraquinone. This study is designed to evaluate the effect of P. zeylanica and naphthoquinone on the level of various amine neurotransmitters namely epinephrine, norepinephrine, serotonin, 5-hydroxyindole 3- acetic acid (5-HIAA), and dopamine on the discrete regions of the brain tissues. Wistar male albino rats were treated separately with ethanoloic extract of P. zeylannica (root) and the commercially purchased phytochemical naphthoquinone at the dose of 2mg/kg b. wt with different experimental groups. The brain tissue homogenates (cerebral cortex, cerebellum, hypothalamus, pons-medulla, midbrain, and corpus striatum) were analyzed to quantify the aforementioned neurotransmitters by high performance liquid chromatography (HPLC). The results showed that, administration of P. zeylanica and NQ does not alter the many of the studied neurotransmitter at significant level; however, there is a change in the neurotransmitter profile in few specific regions of Wistar rat brain and striatum was found to be affected more.

In vitro callus induction and estimation of plumbagin content from Plumbago auriculata Lam.

The medicinal plant Plumbago contains a very potent secondary metabolite, plumbagin having many therapeutic properties. Callus culture was induced using explants, leaf, stem and shoot apex, from P. auriculata. Murashige and Skoog media fortified with various growth hormones like NAA, IAA, IBA and 2, 4-D individually and in various combinations were checked for callus induction. Among the growth hormones used, 1 mg/L 2, 4-D showed best callusing. The hormonal combinations of 1 mg/L IAA and 1.5 mg/L NAA in the media exhibited best callus induction using stem internode as an explant. Plumbagin content from root, stem, leaf and callus was analyzed by using thin layer chromatographic technique. The callus derived from stem showed comparable plumbagin content to the in vivo plant parts. Quantitative spectrophotometric analysis of plumbagin from plant samples and callus indicated that plumbagin content was maximum in roots which was followed by callus, stem and leaf samples respectively. Generation of in vitro sources for plumbagin, for therapeutic applications will serve as a continuous supply and will contribute to preserve the natural plant recourses.

Activity of Plumbago zeylanica Linn. root and Holoptelea integrifolia Roxb. bark pastes in acute and chronic paw infl ammation in Wistar rats.

Background: The pastes prepared from roots of Plumbago zeylanica Linn. and barks of Holoptelea integrifolia Roxb. are widely used by traditional healers for the treatment of arthritis in rural northern Karnataka. Objective: The present study was undertaken to scientifi cally evaluate the safety and effi cacy of traditionally used formulations in experimental animals. Materials and Methods: The study, approved by IAEC was carried out in male Wistar rats and dermal toxicity in rabbits. Carrageenan model was used to assess effect on acute infl ammation. Paw volume were measured at 1, 2, 4, and 6th hour postchallenge. Chronic infl ammation was developed by using Complete Freund’s Adjuvant (CFA). Paw volume, ankle joint circumference, and body weight were assessed on 1st, 4th, 8th, 14th, 17th, and 21st day. Paste was applied once every day to the infl amed area of the paw of respective groups of animals, continuously for 14 days. Statistics: The data were analyzed by one way analysis of variance followed by Dunnett’s post hoc test. P ≤ 0.05 was considered as signifi cant. Results: The formulations did not show any dermal toxicity and found to be safe. Both the pastes signifi cantly (P < 0.05) suppressed, carrageenan-induced paw edema at 6th hour and Holoptelea integrifolia appears to be more effective than Plumbago zeylanica. Signifi cant reduction was observed in paw volume, ankle joint circumference and animal body weight gained. Conclusions: The tested formulations (P. zeylanica root and H. integrifolia bark pastes) showed signifi cant antiinfl ammatory activity. The present fi ndings therefore support its utility in arthritic pain, infl ammation and the claim of traditional practitioners.

Analysis of inorganic elements in the leaves of Plumbago zeylanica L. cultivated by different methods / 中国药学杂志

OBJECTIVE: To study the inorganic elements in the leaves of Plumbago zeylanica L. cultivated by different methods.

Influences of plumbagin on phosphatidylinositol 3-kinase/protein kinase B signaling pathway in rats with hepatic fibrosis / 中华传染病杂志

Objective To explore the influences of plumbagin on phosphatidylinositol 3-kinase (PI3K)/ protein kinase B (Akt) signaling pathway in rats with carbon tetrachloride induced liver fibrosis.Methods Forty male SD rats were assigned to control group,model group,2 mg/kg plumbagin treated group and 3 mg/kg plumbagin treated group,with 10 rats in each group.Rats of the control group were injected with 0.9％ NaCl solution (2 mL/kg) intraperitoneally,while rats of the other three groups were injected with 60％ carbon tetrachloride/peanut oil (2 mL/kg,3 times a week for 6 weeks) intraperitoneally.Since the third week after modeling,rats of plumbagin treated groups were treated with intraperitoneal injection of plumbagin at a dose of 2 mg/kg and 3 mg/kg (twice a week for 4 weeks),respectively.Serum levels of alanine aminotransferase (ALT),aspartate aminotransferase (AST),albumin (Alb) were monitored routinely.Hyaluronic acid (HA) and laminin (LN) were measured by radioimmunoassay after 6 weeks; protein expression of liver PI3K,Akt and phosphorylated Akt (p-Akt) were evaluated by Western blotting and immunohistochemistry,respectively.Comparison of means among groups was performed by univariate analysis of variance.Results The hepatic fibrosis model was successfully established after 6 weeks.Serum levels of ALT,AST,HA and LN of model group were significantly higher than those of control group (all P＜0.05).Serum levels of ALT,AST,HA and LN of 2 mg/kg plumbagin treated group and 3 mg/kg plumbagin treated group were significantly lower than those of model group,and the differences were statistically significant (all P＜0.05).The protein expressions of PI3K and Akt in each group were comparable (all P＞0.05).The p-Akt protein was mainly expressed in nucleus of hepatocytes.The levels of p-Akt protein in control group,model group,2 mg/kg plumbagin treated group and 3 mg/kg plumbagin treated group were 0.0821±0.0003,0.7374±0.0037,0.3679 ±0.0332 and 0.1327±0.0561,respectively,and that in model group was significantly higher than control group (t =851.302,P＜0.05),but those in plumbagin treated groups were both lower than model group (t=71.858 and 28.363,all P＜0.05).Conclusions Plumbagin presents anti-fibrotic effects in the liver,by down-regulating the expression of p-Akt during the development of fibrosis,which might be one of the antifibrotic mechanisms.

A study on nitrogen fixing and phosphate solubilizing microorganisms on growth and Physiology of Plumbago Zeylanica.L.

Organisms that are commonly used as biofertilizers component are nitrogen fixers (N-fixer), potassium solubilizer (K-solubilizer) and phosphorus solubilizer (P- solubilizer), or with the combination of molds or fungi. Most of the bacteria included in biofertilizer have close relationship with plant roots. In this work we have selected plumbago zeylanica.L plant to study the effect of Azotobacter on the growth of roots, stem, and leaves. Also biochemical characterization was done to identify the effect of Azotobacter in Plumbago. The maximum shoot length was recorded in T4 plants (43.51) on 90th days of plant growth after transplanting the plants. There was a significant increase at 5 % level in the root length from 30th days to 90th days in all the treatments. The maximum number of leaves were found in T4 treatment followed by T3 and T2. Minimum numbers of leaves were found in T1 (1083). On 60th day and 90th day also the total chlorophyll content was maximum in T4 treated plants followed by T3, T2 plants. The amount of reducing sugars (μg/g) in shoots of T4, T3 and T2 plants on 30th, 60th and 90th days were significantly high when compared to T1 plants. The content of protein in roots of T2, T3 and T4 plants on 30th, 60th and 90th days were significantly high when compared to protein content of T1 plants.

Determination of Plumbago content in Herba Plumbaginis Zeylanicae under different growing conditions / 中国药学杂志

OBJECTIVE: To determine Plumbago content in Herba Plumbaginis Zeylanicae under different growing conditions and to provide experimental data for its domestication. METHODS: High performance liquid chromatography was used to determine Plumbago contents in the roots, stems and leaves of home-grown Herba Plumbaginis Zeylanicae. RESULTS: Plumbago content in Herba Plumbaginis Zeylanicae grown in mellow and clay soil was higher than in those grown in sand and crude soil. Potasium-fertilized and nitrogen-fertilized Herba Plumbaginis Zeylanicae contained higher Plumbago than those fertilized by phosphorus. Plumbago content was the highest in Herba Plumbaginis Zeylanicae grown in full light. Plumbago contents in roots, stems, and leaves of Herba Plumbaginis Zeylanicae grown under different bred conditions did not vary much. CONCLUSION: The research group's preliminary studies indicated that Plumbago was the main effective ingredient having anti-cancer and anti-inflammation bioactivity. Clay soil, cuttings, potassium fertilizer and nitrogen fertilizer, and full light were thought as ideal conditions for increasing Plumbago content. High quality Herba Plumbaginis Zeylanicae can be grown under these conditions. Copyright 2012 by the Chinese Pharmaceutical Association.

Larvicidal activity of extracts from three Plumbago spp against Anopheles gambiae

Three Plumbago spp have been tested for mosquito larvicidal activity. The crude extracts exhibiting the highest larvicidal activity against Anopheles gambiae were hexane (LC50 = 6.4 μg/mL) and chloroform (LC50 = 6.7 μg/mL) extracts from Plumbago zeylanica Linn, chloroform (LC50 = 6.7 ug/mL) extract from Plumbago stenophylla Bull and ethyl acetate (LC50 = 4.1 μg/mL) extract from Plumbago dawei Rolfe. These LC50 values were within 95 percent confidence limits. 5-hydroxy-2-methyl-1,4-naphthoquinone (plumbagin) 1 (LC50 = 1.9 μg/mL) and β-sitosterol 2 were characterised from ethyl acetate extract of root bark of P. dawei, a native medicinal plant growing in Kenya, based on spectral analysis and comparisons with data in literature.

Preliminary Study on Serum Fingerprint of Plumbago Zeylanica / 中国中医药信息杂志

Objective To sieve the bioactive constituents of Plumbago zeylanica, serum pharmacochemistry research was performed. Method Based on the establishment of HPLC fingerprints of Plumbago zeylanica, the constituents absorbed into blood were determined by comparing the HPLC fingerprints of the methanol extracts, medicated serum samples and blank serum sample. Results One compound absorbed into blood was detected, the other might be metabolites of the original constituent. Conclusion The one onstituent absorbed into blood was possible bioactive component of Plumbago zeylanica.

Antitumor activity of different organic solvents extracts and plumbagin from plumbago zeylanica L. on EMT-6 breast cancer and transplanting S180 in vivo / 中国药理学通报

Aim To find out the effect of the different organic solvents extracts and plumbagin from Plumbago zeylanica L.on EMT-6 breast cancer of BALB/C mouse and transplanted S180 of KM mouse primarily.Method Experiments of animal transplanted tumor in vivo were adopted.Results ① The high dose of chloroform group and plumbagin group could inhibit the growth of EMT-6 breast cancer in BALB/C mice in vivo.Compared with that of physiological saline group,tumor weight has obviously lightened(P

Determination of Trace Elements in Plumbago zeylanica / 中国药房

OBJECTIVE:To establish a determination method for trace elements of Plumbago zeylanica. METHODS:Induct- ively coupled plasma emission spectrum (ICP-AES) was used to determine seven trace elements of P. zeylanica, i.e. Cu, Zn,Fe,Ca,Mg,Mn and Sr simultaneously. Se was determined by atomic fluorescence (AFS) method. RESULTS: The RSD ranged from 0.78% to 3.01%(n=5),while the recovery was within 91.9%～105.8%. The result obtained was satisfactory. Se took a large proportion in P. zeylanica, followed by Cu,Zn,Fe,Ca,Mg,Mn,Sr.CONCLUSION: The method is brief, rapid and accurate for the determination of P. zeylanica. The study provide reference for future pharmacological study of P. zeylanica.