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A Pharmacognostic and Pharmacological Overview on Caesalpinia

A Pharmacognostic and Pharmacological Overview on Caesalpinia

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ISSN: 0975-8585<br />

Anthelmintic activity of leaves of <strong>Caesalpinia</strong> b<strong>on</strong>ducella were investigated for their<br />

anthelmintic activity against Phertima posthuma <str<strong>on</strong>g>and</str<strong>on</strong>g> Ascardia galli.Various c<strong>on</strong>centrati<strong>on</strong> were<br />

used in bioassay.Both extracts showed significant anthelmintic activity [40].<br />

Antifilarial activity<br />

<strong>Caesalpinia</strong> b<strong>on</strong>ducella seed kernel extract <str<strong>on</strong>g>and</str<strong>on</strong>g> fracti<strong>on</strong>s showed microfilaricidal,<br />

macrofilaricidal <str<strong>on</strong>g>and</str<strong>on</strong>g> female sterilizing efficacy against L.sigmod<strong>on</strong>tis <str<strong>on</strong>g>and</str<strong>on</strong>g> microfilaricidal <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

female sterilizing efficacy againsts B.malayi in animal models, indicating the potential of this<br />

plant in providing a lead for new antifilarial drug development [41].<br />

Antiestrogenic activity<br />

Kanchan R,et al., results suggested that alcohol seed extract of <strong>Caesalpinia</strong> b<strong>on</strong>ducella<br />

has antiestrogenic property,possibly acting via inhibiti<strong>on</strong> of estrogen secreti<strong>on</strong> [42].<br />

Antiinflammatory activity<br />

The antiinflammatory activity was studied in rats using the formalin arthritis <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

granuloma pouch methods. At a dose of 250 mg/kg the extract was found to be effective in the<br />

granuloma pouch model <str<strong>on</strong>g>and</str<strong>on</strong>g> compared favourably with phenylbutaz<strong>on</strong>e. The seeds showed a<br />

50% inhibitory activity against carrageenan-induced oedema in the rat hind paw, at an oral<br />

dose of 1000 mg/kg, when given 24 hours <str<strong>on</strong>g>and</str<strong>on</strong>g> 1 hour prior to carrageenan injecti<strong>on</strong> (IP). The<br />

activity (66.67% inhibiti<strong>on</strong>) was comparable to that of phenylbutaz<strong>on</strong>e at a dose of 100 mg/kg<br />

[43-45].<br />

Antimalarial activity<br />

Kalauni SK, et al., has reported antimalarial activity of cassane <str<strong>on</strong>g>and</str<strong>on</strong>g> norcassane type<br />

diterpenes from <strong>Caesalpinia</strong> crista<str<strong>on</strong>g>and</str<strong>on</strong>g> their structure-activity relati<strong>on</strong>ship [46].<br />

Linn T Z, et al. have been reported cassane <str<strong>on</strong>g>and</str<strong>on</strong>g> norcassane type diterpene from<br />

<strong>Caesalpinia</strong> cristaof Ind<strong>on</strong>esia <str<strong>on</strong>g>and</str<strong>on</strong>g> their antimalarial activity against the growth of plasmodium<br />

falciparum [47].<br />

Three new cassane furanoditerpenoids (1-3) together with known cassane diterpenes<br />

were isolated from the seed kernels of caesalpinia b<strong>on</strong>duc.Compounds 1-3 exhibited good<br />

antimalarial activity against multidrug resistant K1 strain of plasmodium falciparum [48].<br />

Antimicrobial activity<br />

Sagar K, et al., reported Antimicrobial activity of α-(2-hydroxy-2-methylpropyl)-ω-(2hydroxy-3-methylbut-2-en-1-yl)<br />

polymethylene from <strong>Caesalpinia</strong> b<strong>on</strong>ducella (L.) Flem [49].<br />

January – March 2012 RJPBCS Volume 3 Issue 1 Page No. 486

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