Extracts from garlic dry powders modulate LPS-induced liberation of cytokines. H.-P. Keiß1, V.M. Dirsch1, T. Hartung2, A.M. Vollmar1 1Department 2Biochemical of Pharmacy, Center of Drug Research, Butenandtstr 5-13, 81377 Munich, Germany Pharmacology, University of Konstanz, Universitaetsstr. 10, 78457 Konstanz, Germany Hans.Keiss@cup.uni-muenchen.de Background: Methods: Garlic (Allium sativum) has been proposed to have anti-atherosclerotic potential, with sulphur compounds seemingly the pharmacologically active substances. Increasing evidence is given that inflammatory processes, such as NF-B activation, cytokine liberation or expression of adhesion molecules, are pivotal in the pathophysiology of atherosclerosis. Garlic extracts Garlic dry powder from unfertilized or sulphur fertilized allium sativum L. cv. Printanor was used. Garlic dry powders were extracted either with aqueous media or DMSO. Cytokine liberation assay Heparinized human whole blood was exposed to respective garlic extracts and stimulated with lipopolysacharide (LPS) 10 ng/ml. Cytokines in the cell free supernatants were collected and subsequently quantified by sandwich ELISA. NF-B luciferase reporter gene assay HEK 293 cells were transfected with a plasmid containing a NF- B driven fireflyluciferase gene and a plasmid containing a HSV-TK driven renilla-luciferase gene. Cells were stimulated with supernatants from the cytokine liberation assay and NF-B promoter activity was measured with a Dual-Luciferase Reporter System. Aim: The aim of our study was to examine the effects of different garlic extracts on cytokine production and to elucidate the impact of increasing amounts of sulphur compounds on the biological activity of the extracts. 1. Liberation of pro-inflammatory cytokines Aqueous extracts DMSO extracts Il-1 TNF- Il-1 TNF- Printanor wo. LPS * * ** 5000 ** 7500 ** wo. LPS g/ m l l 0. m 1 0. 01 m g/ m LP S l m m m g/ - 10 ng/ml LPS + 10 ng/ml LPS unfertilized garlic fertilized garlic • Aqueous extracts liberate Il-1 and TNF- • Aqueous garlic extracts reduce LPS-induced liberation of Il-1 and TNF-, however not dose dependently. • Fertilized garlic shows a weaker pro-inflammatory, but a stronger antiinflammatory potential than unfertilized garlic 1 01 ____________________________ _________________________ __________________________ unfertilized garlic fertilized garlic g/ m l Co g/ m l m 1 0. 01 0. 0. S LP m g/ m l g/ m l 1 0. 01 0. m Co m + 10 ng/ml LPS * 0 m g/ 10 ________________________________ - 10 ng/ml LPS unfertilized garlic fertilized garlic * 5000 2500 m g/ m l l l l m g/ m m 1m g/ 0, ______________________________ + 10 ng/ml LPS 1 l LP S m g/ m 1 0, m l l Co m 1 10 l m g/ m g/ _________________________ __________________________ 10000 10000 0 0 10 0. 1 1 m m g/ m m l l m l LP S g/ m 10 0. 1 1 m m g/ g/ m m l l Co 0 Printanor 12500 15000 0. 5000 m ** 10000 g/ m * 10000 15000 g/ 20000 Il-1 [pg/ml Blood] TNF [pg/ml Blood] Il-1 [pg/ml Blood] 20000 30000 20000 Printanor TNF [pg/ml Blood] Printanor 40000 _____________________________ + 10 ng/ml LPS unfertilized garlic fertilized garlic • DMSO extracts do not liberate Il-1 and TNF- • DMSO extracts reduce LPS-induced liberation of Il-1 and TNF- • Fertilization has no influence on the inhibitory effect 3. NF-B activity assay To investigate whether the modulation of cytokine levels in human whole blood leads to a change in the transactivation activity of the transcription factor NF- B we performed a NF- B-luciferase reporter gene assay. Therefore cells were transfected as described under methods and subsequently stimulated with the supernatants of human blood, treated with DMSO garlic extracts and LPS or with LPS alone. 2. Liberation of anti-inflammatory cytokine DMSO extracts Il-10 Printanor 500 l l m m g/ g/ ** 5.0 ** ** unfertilized garlic fertilized garlic m 2.5 1 • Aqueous garlic extracts liberate Il-10 • Aqueous extracts increase LPS-induced liberation of Il-10 • Low concentrations of DMSO garlic extracts increase LPS-induced liberation of Il-10 • High concentrations of aqueos fertilized garlic extract show a strong inhibitory effect on Il-10 liberation l m g/ m 0, 1 m 0, 01 g/ m g/ m m l l m g/ m l 0.0 LP S + 10 ng/ml LPS unfertilized garlic fertilized garlic 0, 01 __________________________ - 10 ng/ml LPS unfertilized garlic fertilized garlic 0. ___________________________ 0. 01 m m g/ m 1 m LP S l l m Co g/ 0. + 10 ng/ml LPS 01 _____________________________ - 10 ng/ml LPS 0. 1 m g/ m l 10 m g/ m l l m 1m g/ 0. ____________________________ LP S l g/ m l 10 m g/ m l 1 m m 1m g/ 0. Co 0 7.5 o 0 10.0 C 500 * 1000 x-fold luciferase activity 1000 NF- B activity assay Printanor 1500 ** 1500 Il-10 [pg/ml Blood] Il-10 [pg/ml Blood] 2000 0, 1 Aqueous extracts DMSO garlic extract + LPS • Supernatants of blood cells treated with DMSO garlic extracts reduce NF-B activity • Fertilized garlic was more active than unfertilized garlic * < 0.05 Anova with Bonferroni post-test ** < 0.01 Anova with Bonferroni post-test Conclusion: This study indicates, that garlic dry powder extracts are able to decrease LPS-induced liberation of pro-inflammatory cytokines Il-1 and TNF-. On the other hand, they can increase the liberation of the anti-inflammatory cytokine Il-10. These effects are strongly dependent on the solvent used for extraction. Furthermore, it was shown that sulphur fertilization may have a positive influence on the action mediated by garlic. In summary, DMSO garlic extracts modify cytokine release from human blood in a way possibly resulting in a lower expression of NF- B regulated genes. This work was supported by the EU : “Garlic and Health Project”, Id-Nr: QLK1-CT-1999-00498