EXPERIMENTAL IMMUNOLOGY
Different effects of feeding pregnant and lactating mice Rhodiola kirilowii aqueous and hydro-alcoholic extracts on their serum angiogenic activity and content of selected polyphenols
More details
Hide details
Submission date: 2016-10-20
Final revision date: 2016-10-27
Acceptance date: 2016-10-28
Publication date: 2017-05-08
Cent Eur J Immunol 2017;42(1):17-23
KEYWORDS
ABSTRACT
Angiogenesis plays an important role in many physiological processes, among them the formation of tissues and organs during embryogenesis. A lot of medicinal plants exhibit angiomodulatory properties. This creates the need for a thorough check of whether the plant extracts that we would like to give to pregnant women in order to increase their resistance to bacterial or viral infection will have negative effects on angiogenesis, and consequently on fetal development. This paper seeks to investigate the effect of serum of pregnant and nursing Balb/c mice that received aqueous (RKW) or hydro-alcoholic (RKW-A) R. kirilowii extracts (20 mg/kg), or epigallocatechin (0.2 mg/kg), on the in vitro proliferation and migration of mouse endothelial cell line HECa10. Of the 15 identified polyphenols in the extracts by HPLC, 8 were present in the sera. Chemical analysis revealed higher salidroside, kaempferol, chlorogenic acid, bFGF and VEGF concentration in RKW-A sera than in the sera of RKW group of mice. RKW-A and EGC sera did not affect migration of endothelial cells, however we noted some increase of migrating cells after RKW-sera treatment. RKW and EGC sera did not affect proliferation of endothelial cells. Sera of mothers from RKW-A group impaired the proliferation of endothelial cells in comparison to other groups. These data allow us to assume that Rhodiola kirilowii hydro-alcoholic extract (RKW-A) is potentially able to modulate pre- and post- natal angiogenesis what might influence the development of organs in progeny. Sera of RKW mothers have not harm the proliferation of endothelial cells, despite they also contain antiangiogenic catechins and salidroside. This suggests the existence in RKW-A extract and in RKW-A sera of some other, as yet unidentified substances influencing endothelial cells proliferation.
REFERENCES (25)
1.
Zdanowski R, Lewicki S, Sikorska K, et al. (2014): The influence of aqueous and hydro-alcoholic extracts of roots and rhizomes of Rhodiola kirilowii on the course of pregnancy in mice. Cent Eur J Immunol 39: 471-475.
2.
Radomska-Leśniewska D, Skopiński P, Bałan BJ, et al. (2015): Angiomodulatory properties of Rhodiola spp. and other natural antioxidants. Cent Eur J Immunol 40: 249-262.
3.
Siwicki AK, Skopinska-Różewska E, Hartwich M, et al. (2007): The influence of Rhodiola rosea extracts on non-specific and specific cellular immunity in pigs, rats and mice. Cent Eur J Immunol 32: 84-91.
4.
Wójcik R, Siwicki AK, Skopińska-Różewska E, et al. (2009): The effect of Chinese medicinal herb Rhodiola kirilowii extracts on cellular immunity in mice and rats. Pol J Vet Sci 12: 399-405.
5.
Skopinska-Różewska E, Bychawska M, Białas-Chromiec B, Sommer E (2009): The In vivo effect of Rhodiola rosea and Rhodiola quadrifida hydro-alcoholic extracts on chemokinetic activity of spleen lymphocytes in mice. Centr Eur J Immunol 34: 42-45.
6.
Skopińska-Różewska E, Bychawska M, Białas-Chromiec B, et al. (2010): The in vivo effect of Rhodiola kirilowii extracts on blood granulocytes metabolic activity in mice. Cent Eur J Immunol 35: 20-24.
7.
Siwicki A, Skopińska-Różewska E, Wasiutyński A, et al. (2012): The effect of Rhodiola kirilowii extracts on pigs blood leukocytes metabolic (RBA) and proliferative (LPS) activity, and on the bacterial infection and blood leukocytes number in mice. Centr Eur J Immunol 37: 145-150.
8.
Zdanowski R, Lewicki S, Skopińska-Różewska E, et al. (2014): Alcohol- and water-based extracts obtained from Rhodiola rosea affect differently the number and metabolic activity of circulating granulocytes in Balb/c mice. Ann Agric Environ Med 21: 120-123.
9.
Skopinska-Różewska E, Hartwich M, Siwicki AK, et al. (2008): The influence of Rhodiola rosea extracts and rosavin on cutaneous angiogenesis induced in mice after grafting of syngeneic tumor cells. Centr Eur J Immunol 33: 102-107.
10.
Skopińska-Różewska E, Malinowski M, Wasiutyński A, et al. (2008): The influence of Rhodiola quadrifida 50% hydro-alcoholic extract and salidroside on tumor-induced angiogenesis in mice. Pol J Vet Sci 11: 97-104.
11.
Zdanowski R, Skopinska-Różewska E, Wasiutyński A, et al. (2012): The effect of Rhodiola kirilowii extracts on tumor-induced angiogenesis in mice. Centr Eur J Immunol 37: 131-139.
12.
Lewicki S, Stankiewicz W, Skopińska-Różewska E, et al. (2015): Spleen content of selected polyphenols, splenocytes morphology and function in mice fed Rhodiola kirilowii extracts during pregnancy and lactation. Pol J Vet Sci 18: 847-855.
13.
Shin JW, Seol IC, Son CG (2010): Interpretation of animal dose and human equivalent dose for drug development. J Korean Oriental Med 31: 1-7.
14.
Bizouarne N, Denis V, Legrand A, et al. (1993): A SV-40 immortalized murine endothelial cell line from peripheral lymph node high endothelium expresses a new alpha-L-fucose binding protein. Biol Cell 79: 209-218.
15.
Kieda C, Paprocka M, Krawczenko A, et al. (2002): New human microvascular endothelial cell lines with specific adhesion molecule phenotypes. Endothelium 9: 247-261.
16.
Skopiński P, Zdanowski R, Grzela T, et al. (2012): The influence of sterilized and non-sterilized amniotic dressings on the proliferation of endothelial cells in vitro. Cent Eur J Immunol 37: 114-118.
17.
Rokicki D, Zdanowski R, Lewicki S, et al. (2014): Inhibition of proliferation, migration and invasiveness of endothelial murine cells culture induced by resveratrol. Cent Eur J Immunol 39: 449-454.
18.
Irchhaiya R, Kumar A, Yadav A, et al. (2014): Metabolites in plants and its classification. World J Pharm Pharmac Sci 4: 287-305.
19.
Zhou T, Zheng J, Zhou Y, et al. (2015): Chemical Components and Bioactivities of Rhodiola rosea. Int J Trad Nat Med 5: 23-51.
20.
Skopiński P, Skopińska-Różewska E, Kamiński A, et al. (2004): Chocolate feeding of pregnant mice resulted in epigallocatechin- related embryonic angiogenesis suppression and bone mineralization disorder. Pol J Vet Sci 7: 131-133.
21.
Wasiutyński A, Siwicki AK, Bałan BJ, et al. (2005): Inhibitory effect of cocoa catechins on embryonic and tumor angiogenesis in mice. Pol J Environm Studies 14: 800-805.
22.
Sun KX, Xia H, Xia RL (2015): Anticancer effect of salidroside on colon cancer through inhibiting JAK2/STAT3 signaling pathway. Int J Clin Exp Pathol 8: 615-621.
23.
Wang J, Li JZ, Lu AX, et al. (2014): Anticancer effect of salidroside on A549 lung cancer cells through inhibition of oxidative stress and phospho-p38 expression. Oncol Lett 7: 1159-1164.
24.
Liang J, Xu F, Zhang YZ, et al. (2014): The profiling and identification of the metabolites of (+)-catechin and study on their distribution in rats by HPLC-DAD-ESI-IT-TOF-MS(n) technique, Biomed Chromatogr 28: 401-411.
25.
Blount JW, Redan BW, Ferruzzi MG, et al. (2015): Synthesis and quantitative analysis of plasma-targeted metabolites of catechin and epicatechin, J Agric Food Chem 63: 2233-2240.