Abstract
This chapter deals with the biochemical pharmacology depicted by the plant Artemisia amygdalina. The important biological activities that have been reported till date include those of free radical scavenging potential of the in vitro raised and greenhouse acclimatized plants, anti-inflammatory, and immunomodulatory activity of the plant and the anti-diabetic and anti-hyperlipidemic effect of A. amygdalina. The methanolic extract of the in vitro grown and greenhouse acclimatized plants revealed the highest inhibitory activity, 92.11 and 91.2 % (IC50 = 26.06 µg mL−1), respectively, against DPPH radical. Carrageenan paw edema model has been employed to study the potential of the plant extracts in inflammation in wistar rats. SRBC-specific haemagglutination-titer and DTH assays have been carried out in Balb/C mice for observing the effect of extracts on immune system. The methanolic fraction has been observed to have the maximum effect on the inhibition of paw edema formation with the inhibitory potential of 42.26 %, while in the immunomodulation studies the plant extracts have been found to have the immunosuppressant activity with methanolic fraction again showing the maximum potential for the suppression of both humoral (55.89 and 47.91 %) and cell-mediated immunity (62.27 and 57.21 %). Petroleum ether, ethyl acetate, methanol, and hydroethanolic extracts of A. amygdalina have been tested for their anti-diabetic potentials in diabetic rats. The hydroethanolic and methanolic extracts each at doses of 250 and 500 mg/kg b.w. have significantly reduced glucose levels in diabetic rats. The other biochemical parameters like cholesterol, triglycerides, low density lipoproteins (LDL), serum creatinine, serum glutamate pyruvate transaminase (SGPT), serum glutamate oxaloacetate transaminase (SGOT), and alkaline phosphatise (ALP), have been found to be reduced by the hydroethanolic and methanolic extracts. The extracts have also shown reduction in the feed and water consumption of diabetic rats when compared with the diabetic control.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Bhagwat DP, Kharya MD, Banietal S (2010) Indian J Pharmacol 42:21–26
Gazafar K, Ganaie BA, Seema A, Mubashir K, Showkat AD, Younis Dar M, Tantry M (2014) BioMed Res Int 1–10
Jayathirtha MG, Mishra SH (2004) Phytomedicine 11:361–365
Lunardelli A, Leite CE, Pires MGS, deOliveira JR (2006) Inflamm Res 55:129–135
Mangathayaru K, Umadevi M, Reddy CU (2009) J Ethnopharmacol 123:181–184
Mubashir K, Ganaie BA, Gazafar K, Seema A, Akhter HM, Akbar M (2013) ISRN Inflammation 2013:1–6
Organisation for Economic Cooperation and Development (2008) OECD guidelines for the testing of chemicals Test 425
Rasool R, Ganaie BA, Akbar S, Kamili AN (2013) Chin J Nat Med 11:0377–0384
Suffredini AF, Fantuzzi G, Badolato R, Oppenheim JJ, O’Grady NP (1999) J Clin Immunol 19:203–214
Thakur M, Connellan P, Deseo MA, Morris C, Dixit VK (2011) Evidence-based complementary and alternative medicine 7:1–7
Winter CA, Risley EA, Nuss GW (1962) Proc Soc Exp Biol Med 111:544–547
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
Copyright information
© 2015 The Author(s)
About this chapter
Cite this chapter
Lone, S.H., Bhat, K.A., Khuroo, M.A. (2015). Biological Profile of Artemisia amygdalina . In: Chemical and Pharmacological Perspective of Artemisia amygdalina. SpringerBriefs in Pharmacology and Toxicology. Springer, Cham. https://doi.org/10.1007/978-3-319-25217-9_5
Download citation
DOI: https://doi.org/10.1007/978-3-319-25217-9_5
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-25215-5
Online ISBN: 978-3-319-25217-9
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)