05.02.2014 Views

Ber and other Jujubes monograph.pdf - Crops for the Future

Ber and other Jujubes monograph.pdf - Crops for the Future

Ber and other Jujubes monograph.pdf - Crops for the Future

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

2.3.4.2 Glycosides/saponins<br />

The glycoside saponin is found in <strong>the</strong> seeds, leaf <strong>and</strong> stem of Z. jujuba<br />

(Ogihara et al., 1976). Saponins are part of sugar chains which attach<br />

<strong>the</strong>mselves to a sterol or triterpene. They are known to bind with cholesterol<br />

preventing it from being reabsorbed into <strong>the</strong> system. They are being widely<br />

researched <strong>for</strong> cancer prevention <strong>and</strong> cholesterol control. Ogihara (1976)<br />

developed a method <strong>for</strong> successful qualitative <strong>and</strong> quantitative determination of<br />

saponins in Z. jujuba seeds using counter current chromatography.<br />

The saponins isolated from <strong>the</strong> seeds of Z .jujuba include jujubosides A, B<br />

(ZengL et al., 1987), A1 B1 <strong>and</strong> C <strong>and</strong> acetyljujuboside B (Yoshikawa et al.,<br />

1997) <strong>and</strong> <strong>the</strong> protojujubosides A, B <strong>and</strong> B1 (Matsuda et al., 1999).<br />

Kurihara et al. (1988) extracted <strong>the</strong> saponin, ziziphin, from <strong>the</strong> dried leaves of<br />

Z. jujuba. It has a structure, 3-O-a-L-rhamnopyranosyl (1-2)-a-Larabinopyranosyl-20-O-<br />

(2,3)-di-O-acetyl-a-L-rhamnopyranosyl jujubogenin.<br />

Ikram et al. (1981) isolated a saponin from Z .jujuba leaves <strong>and</strong> stem. It was<br />

assigned <strong>the</strong> structure 3-O- ((2-O- alpha – D – furopyranosyl – 3-O- beta – D –<br />

glucopyranosyl) – alpha – L – arabinopyranosyl) jujubogenin. Jujubogenin was<br />

also found in extract of Z. mauritiana leaves (Sharma <strong>and</strong> Kumar, 1982).<br />

Saponins show adjuvant (Oda et al., 2000), haemolytic (Oda et al., 2000),<br />

sedative (Shou et al., 2002) anxiolytic <strong>and</strong> sweetness inhibiting properties<br />

(Kurihara et al., 1988). Jujuboside A (JuA), is also known to be a noncompetitive<br />

inhibitor of calmodulin (Zhou et al., 1994), which is an ubiquitous,<br />

calcium-binding protein that can bind to <strong>and</strong> regulate a multitude of different<br />

protein targets, <strong>the</strong>reby affecting many different cellular functions. CaM<br />

mediates processes such as inflammation, metabolism, muscle contraction,<br />

short-term <strong>and</strong> long-term memory, <strong>and</strong> <strong>the</strong> immune response (McDowall,<br />

2003). Jujuboside inhibition of calmodulin is thought to be linked to its<br />

sedative properties (Zhou et al., 1994).<br />

2.3.5 Triterpenoic acids<br />

The following triterpenoic acids have been isolated from <strong>the</strong> fruits of Z. jujuba:<br />

colubrinic acid, alphitolic acid, 3-O-cis-p-coumaroylalphitolic acid, 3-O-transp-coumaroylalphitolic<br />

acid, 3-O-cis-p-coumaroylmaslinic acid, 3-O-trans-pcoumaroylmaslinic<br />

acid, oleanolic acid, betulonic acid, oleanonic acid,<br />

zizyberenalic acid <strong>and</strong> betulinic acid (Lee et al., 2003). Triterpenoic acids have<br />

shown cytotoxic effects on tumour cell lines (Eiznhamer <strong>and</strong> Xu, 2004).<br />

Triterpenoic acids have also been extracted from roots of Z. mauritiana (Kundu<br />

et al. 1989).<br />

22

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!