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1.
Asian Pac J Cancer Prev ; 14(4): 2599-605, 2013.
Article in English | MEDLINE | ID: mdl-23725182

ABSTRACT

The study aimed to evaluate immune-stimulating effects of a well-known Thai folkloric remedy when used for adjuvant therapy with conventional chemotherapeutics for treatment of breast cancer. Immunostimulating influence of the remedy (215 mg/kg body weight per day) on NK cell activity and TNF-α release from the monocytes/macrophages were investigated in a total of 15 healthy women and 13 female patients with breast cancer (Group 1). The effect of breast tumor surgery on NK cell activity was further investigated in 18 female patients with breast cancer (Group 2). NK cell cytotoxic activity was determined by chromium release cytotoxic assay using K562, an erythroleukemic cell line. TNF-α release from monocytes/macrophages separated from blood samples was determined through a biological assay using actinomycin D-treated L929 mouse fibroblast cells in the presence and absence of LPS. Baseline NK cell activity of the monocytes/macrophages separated from Group 2 patients expressed as %cytotoxicity was significantly lower than in the healthy subjects at E:T ratios of 100:1 and 25:1. In healthy subjects, there was no change in NK cell cytotoxic activity (%cytotoxicity or LU) following 1 and 2 weeks of treatment with the remedy compared with the baseline at various E:T ratios but the binding activity (%binding) was significantly increased after 2 weeks of treatment. The addition of one or two conventional chemotherapeutic regimens did not significantly reduce the NK cytotoxic activity but did affect release of TNF-α in both unstimulated and LPS-stimulated samples. Surgery produced a significant suppressive effect on NK cell activity. The use of the remedy as an adjunct therapy may improve therapeutic efficacy and safety profiles of conventional chemotherapeutic regimens through stimulation of the immune system in cancer patients.


Subject(s)
Adenocarcinoma/immunology , Breast Neoplasms/immunology , Cytotoxicity, Immunologic/immunology , Killer Cells, Natural/immunology , Phytotherapy , Plant Extracts/pharmacology , Plants, Medicinal , Adenocarcinoma/pathology , Adenocarcinoma/therapy , Adult , Animals , Breast Neoplasms/pathology , Breast Neoplasms/therapy , Case-Control Studies , Dactinomycin/pharmacology , Female , Fibroblasts/drug effects , Fibroblasts/immunology , Follow-Up Studies , Humans , Killer Cells, Natural/drug effects , Lipopolysaccharides/pharmacology , Lymphocyte Activation/drug effects , Macrophages/drug effects , Macrophages/immunology , Mice , Mice, Inbred C3H , Middle Aged , Monocytes/drug effects , Monocytes/immunology , Prognosis , Tumor Necrosis Factor-alpha/pharmacology
2.
Planta Med ; 73(6): 503-11, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17650544

ABSTRACT

Andrographis paniculata has been widely used as a traditional medicine for the treatment of common cold, diarrhea and hypertension. The three major active diterpenoids are andrographolide (AP1), 14-deoxy-11,12-didehydroandrographolide (AP3) and neoandrographolide (AP4). It has been reported that AP3 has hypotensive and vasorelaxation effects. However, there is only limited information on the cardiovascular effects of the other diterpenoids and crude extracts containing different levels of AP3. Therefore, the present study investigated the effects of these diterpenoids, AP1, AP3, and AP4, isolated from A. paniculata, and different aqueous plant extracts on blood pressure, vascular and chronotropic responses by using conscious rats and their isolated aortas and right atria as the test models. Among the three major diterpenoids, AP3 was the most potent compound for inducing vasorelaxation and decreasing heart rate. In addition, Extract B (high level of AP3) had greater hypotensive effect in conscious rats than Extract A (low level of AP3). Verapamil, a Ca2+ channel blocker, also had a hypotensive effect less than that of Extract C containing a high level of AP3. At the doses and durations of Extract A and B which produced hypotension, the responses of the Extract A-treated aorta to norepinephrine, and the vascular muscarinic responses to acetylcholine of both extracts were decreased. However, repeated doses of both extracts did not alter cardiac beta-adrenoceptor and muscarinic responses of extract-treated rats to NE and ACh, respectively. The results of this study suggest that vascular smooth muscle is the major site of these hypotensive effects of both AP3 and A. paniculata extracts. Furthermore, the consumption of A. paniculata products containing high levels of AP3 may be responsible for causing hypotension in some patients taking this herbal drug.


Subject(s)
Andrographis , Antihypertensive Agents/pharmacology , Cardiovascular System/drug effects , Diterpenes/pharmacology , Phytotherapy , Animals , Antihypertensive Agents/administration & dosage , Antihypertensive Agents/therapeutic use , Aorta, Thoracic/drug effects , Blood Pressure/drug effects , Diterpenes/administration & dosage , Diterpenes/therapeutic use , Dose-Response Relationship, Drug , Heart Atria/drug effects , Heart Rate/drug effects , Male , Muscle Contraction/drug effects , Plant Components, Aerial , Plant Extracts/administration & dosage , Plant Extracts/pharmacology , Plant Extracts/therapeutic use , Rats , Rats, Wistar
3.
Eur J Pharmacol ; 553(1-3): 39-45, 2006 Dec 28.
Article in English | MEDLINE | ID: mdl-17081514

ABSTRACT

Andrographis paniculata has been widely used for the prevention and treatment of common cold especially in Asia and Scandinavia. The three active diterpenoids from this plant, including aqueous plant extracts, were investigated for the inhibitory effect on platelet aggregation in vitro. The results indicated that andrographolide (AP(1)) and 14-deoxy-11,12-didehydroandrographolide (AP(3)) significantly inhibited thrombin-induced platelet aggregation in a concentration-(1-100 microM) and time-dependent manner while neoandrographolide (AP(4)) had little or no activity. AP(3) exhibited higher antiplatelet activity than AP(1) with IC(50) values ranging from 10 to 50 microM. The inhibitory mechanism of AP(1) and AP(3) on platelet aggregation was also evaluated and the results indicated that the inhibition of extracellular signal-regulated kinase1/2 (ERK1/2) pathway may contribute to antiplatelet activity of these two compounds. In addition, standardized aqueous extracts of A. paniculata containing different amounts of AP(3) inhibited thrombin-induced aggregation to different degrees. The extracts significantly decreased platelet aggregation in a concentration-(10-100 microg/ml) and time-dependent manner. However, the extract with high level of AP(3) (Extract B) (IC(50) values=50-75 microg/ml) showed less inhibitory activity against thrombin than the extract with lower level of AP(3) (Extract A) (IC(50) values=25-50 microg/ml). These results indicate that the standardized A. paniculata extract may contain other antiplatelet compounds rather than AP(1) and AP(3), which contribute to high antiplatelet activity. Therefore, the consumption of A. paniculata products may help to prevent or treat some cardiovascular disorders i.e. thrombosis; however, it should be used with caution by patients with bleeding disorders.


Subject(s)
Andrographis/chemistry , Diterpenes/pharmacology , Glucosides/pharmacology , Platelet Aggregation/drug effects , Tetrahydronaphthalenes/pharmacology , Animals , Blood Platelets/drug effects , Blood Platelets/enzymology , Diterpenes/chemistry , Dose-Response Relationship, Drug , Extracellular Signal-Regulated MAP Kinases/metabolism , Glucosides/chemistry , In Vitro Techniques , Indicators and Reagents , Male , Phosphorylation , Plant Extracts/chemistry , Plant Extracts/pharmacology , Rats , Rats, Wistar , Tetrahydronaphthalenes/chemistry
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