Salvianolic acid B: in vitro and in vivo effects on the immune system

Authors

Keywords:

salvianolic acid B, type 1 diabetes, macrophage, lymphocyte, immune modulation

Abstract

Type 1 diabetes (T1D) is an autoimmune disorder with a strong inflammatory component. Autoreactive cells specifically target insulin-producing β-cells, which leads to loss of glucose homeostasis. T1D remains incurable and versatile; potentially beneficial therapeutics are being tested worldwide. Possible candidates for the treatment of autoimmune diabetes are plants and their extracts since they are rich in biophenols, substances that act as secondary metabolites, and have verified antioxidant and antiinflammatory effects. Salvianolic acid B (SalB) is a biophenol and one of the major constituents of Origanum vulgare ssp. hirtum (Greek oregano) extracts which in our previous studies was shown to exhibit an antidiabetic effect in mice. The aim of the present study was to determine whether SalB is responsible for the observed effects of Greek oregano extracts. SalB was applied in vitro to macrophages and lymphocytes isolated from C57BL/6 mice, as well as in vivo in the model of T1D induced by multiple low doses (MLD) of streptozotocin (STZ). SalB did not affect the viability of cells, but it significantly decreased secretion of nitric oxide (NO) and TNF in lipopolysaccharide (LPS)-stimulated macrophages, as well as the secretion of IFN-γ in concanavalin A (ConA)-stimulated lymphocytes. However, when applied in vivo, SalB at a dose of 2.5 mg/kg b.w., applied for 10 consecutive days, failed to protect mice from diabetes development. In conclusion, SalB exerts immunomodulatory effects in vitro, but is not effective in prevention of T1D in vivo. It probably requires cooperation with some other substances for the maximum efficacy exhibited by oregano extracts.

https://doi.org/10.2298/ABS170216011V

Received: February 16, 2017; Revised: March 14, 2017; Accepted: March 24, 2017; Published online: April 4, 2017

How to cite this article: Vujičić M, Saksida T, Stojanović I. Salvianolic acid B: In vitro and in vivo effects on the immune system. Arch Biol Sci. 2017;69(4):659-63.

Downloads

Download data is not yet available.

References

Anderson RP, van Heel DA, Tye-Din JA, Barnardo M, Salio M, Jewell DP, Hill AVS. T cells in peripheral blood after gluten challenge in coeliac disease. Gut 2005;54(9):1217-23.

Maahs DM, Rewers M. Editorial: mortality and renal disease in type 1 diabetes mellitus − progress made, more to be done. J Clin Endocrinol Metab. 2006;91:3757-9.

Hakonarson H, Grant S. Genome-wide association studies (GWAS): impact on elucidating the aetiology of diabetes. Diabetes Metab Res Rev. 2011;27(7):685-96.

Makino S, Kunimoto K, Muraoka Y, Mizushima Y, Katagiri K, Tochino Y. Breeding of a non-obese, diabetic strain of mice. Jikken Dobutsu. 1980;29:1-13.

Bluestone J, Herold K, Eisenbarth G. Genetics, pathogenesis and clinical interventions in type 1 diabetes. Nature. 2010;464:1293-300.

Emamaullee JA, Davis J, Merani S, Toso C, Elliott JF, Thiesen A, Shapiro AM. Inhibition of Th17 cells regulates autoimmune diabetes in NOD mice. Diabetes. 2009;58(6):1302-11.

Hill NJ, Van GK, Sarvetnick N. Th1 and Th2 pancreatic inflammation differentially affects homing of islet-reactive CD4 cells in nonobese diabetic mice. J Immunol. 2003;170:1649-58.

Tarbell KV, Yamazaki S, Olson K, Toy P, Steinman RM. CD25+ CD4+ T cells, expanded with dendritic cells presenting a single autoantigenic peptide, suppress autoimmune diabetes. J Exp Med. 2004;199:1467-77.

Cavan D, Fernandes JR, Makaroff L, Ogurtsova K, Webber S, editors. IDF DIABETES ATLAS. 7th ed. Brussels: International Diabetes Federation; 2015. 144p.

Jaganath IB, Crozier A. Overview of health promoting compounds in fruits and vegetables. In: Chichester FC, editor. Phenolic Compounds of Plant Origin and Health: The Biochemistry Behind Their Nutritional and Pharmacological Value. United Kingdom: Wiley; 2009. p. 1-48.

Del Rio D, Rodriguez-Mateos A, Spencer JPE, Tognolini M, Borges G, Crozier A. Dietary (poly)phenolics in human health: structures, bioavailability, and evidence of protective effects against chronic diseases. Antioxid Redox Signal. 2013;18;(14):1818-92.

Vujicic M, Nikolic I, Kontogianni VG, Saksida T, Charisiadis P, Orescanin-Dusic Z, Blagojevic D, Stosic-Grujicic S, Tzakos AG, Stojanovic I. Methanolic extract of Origanum vulgare ameliorates type 1 diabetes through antioxidant, anti-inflammatory and anti-apoptotic activity. Br J Nutr. 2015;113(5):770-82.

Vujicic M, Nikolic I, Kontogianni VG, Saksida T, Charisiadis P, Vasic B, Stosic-Grujicic S, Gerothanassis I P, Tzakos AG, Stojanovic I. Ethyl Acetate Extract of Origanum vulgare L. ssp. hirtum Prevents Streptozotocin-Induced Diabetes in C57BL/6 Mice. J Food Sci. 2016;81:H1846-H1853.

Wang J, Xiong X, Feng B. Cardiovascular Effects of Salvianolic Acid B. Evid Based Complement Alternat Med. 2013;2013:247948.

Stojanovic I, Saksida T, Nikolic I, Nicoletti F, Stosic-Grujicic S. Macrophage migration inhibitory factor deficiency protects pancreatic islets from cytokine-induced apoptosis in vitro. Clin Exp Immunol. 2012;169:156-63.

Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65:55-63.

Jimal R, Shimogawara R, Yamamoto K, Ohta N. Anti-trypanosome effects of nutritional supplements and vitamin D3: in vitro and in vivo efficacy against Trypanosoma brucei brucei. Trop Med Health 2016;44:26.

Sun B, Li C, Zuo L, Liu P. Protection of SAL B with H9C2 cells. Pharm Biol. 2016;54(5):889-95.

Oh KS, Oh BK, Mun J, Seo HW, Lee BH. Salvianolic acid A suppress lipopolysaccharide-induced NF-κB signaling pathway by targeting IKKβ. Int Immunopharmacol. 2011;11(11):1901-6.

Zhao X, Jia H, Yang S, Liu Y, Deng B, Xu X, Zhang T, Zhou H, Zu C, Yin H, Li T, Song Y, Wang Y, Li P, Zou Z, Cai D. Salvianolic Acid B reducing portal hypertension depends on macrophages in isolated portal perfused rat livers with chronic hepatitis. Evid Based Complement Alternat Med. 2012;2012:786365.

Donga Z, Maa D, Gong Y, Yu T, Yao G. Salvianolic acid B ameliorates CNS autoimmunity by suppressing Th1 responses. Neurosci Lett. 2016;619(21):92-9.

Raoufi S, Baluchnejadmojarad T, Roghani M, Ghazanfari T, Khojasteh F, Mansouri M. Antidiabetic potential of salvianolic acid B in multiple low-dose streptozotocin-induced diabetes. Pharm Biol. 2015;53(12):1803-9.

Shao S, He F, Yang Y, Yuan G, Zhang M, Yu X. Th17 cells in type 1 diabetes. Cell Immunol. 2012;280(1):16-21.

Anderson MS, Bluestone JA. The NOD mouse: a model of immune dysregulation. Annu Rev Immunol. 2005;23:447-85.

Downloads

Published

2017-10-18

How to Cite

1.
Vujičić M, Saksida T, Stojanović I. Salvianolic acid B: in vitro and in vivo effects on the immune system. Arch Biol Sci [Internet]. 2017Oct.18 [cited 2024Dec.22];69(4):659-63. Available from: https://serbiosoc.org.rs/arch/index.php/abs/article/view/1477

Issue

Section

Articles

Most read articles by the same author(s)