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Medicinal Plants Classification Biosynthesis and ... - Index of

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222<br />

S.M.M. Vasconcelos, J.E.R. Honório Júnior, R.N.D. Cavalcante de Abreu et al.<br />

2.1. Pro-inflammatory, Anti-inflammatory <strong>and</strong> Allergenic Properties<br />

C. procera latex is well known for its medicinal <strong>and</strong> toxic properties. When locally<br />

administered, latex induces an intense inflammatory process that can be characterized by<br />

increase in vascular permeability, edema <strong>and</strong> cellular infiltrate (Padhy, Kumar, 2005). Such<br />

inflammation is due to histamine derived from mast cells <strong>and</strong> also to the histamine present in<br />

the latex. Thus, anti-histamine drugs can be used in the treatment <strong>of</strong> inflammation caused by<br />

the exposition to the latex <strong>of</strong> this plant (Shivkar, Kumar, 2003).<br />

The inflammation caused by latex has been demonstrated by many experimental models<br />

<strong>of</strong> inflammation, such as paw edema, air bag (Singh et al., 2000) <strong>and</strong> rat pleurisies (Shivkar,<br />

Kumar, 2003). Thus, latex is a potent flogistic agent that may be useful as a tool for research<br />

<strong>of</strong> new anti-inflammatory drugs.<br />

The inflammatory effects caused by proteins present in dried latex can be effectively<br />

inhibited by cyproheptadine <strong>and</strong> refecoxib. The latter is superior to dicl<strong>of</strong>enac in ameliorating<br />

the hyperalgesia induced by DL (Sehgal, Kumar, 2005).<br />

However, latex has also anti-inflammatory effects. Oral administration <strong>of</strong> aqueous<br />

methanolic latex extract inhibited edema induced by carragenin <strong>and</strong> formalin. Histological<br />

analysis demonstrated that latex extract was more potent than phenylbutazone to inhibit the<br />

cellular infiltrate <strong>and</strong> subcutaneous edema induced by carragenin, suggesting that latex<br />

inhibits mainly histamine <strong>and</strong> bradykinin (Arya, Kumar, 2005).<br />

Latex inhibited inflammation in models <strong>of</strong> paw edema <strong>and</strong> air bag in rat experiments<br />

(Kumar, Basu, 1994). Treatment with methanolic extract inhibits articular inflammation,<br />

probably due to reduction <strong>of</strong> cellular influx <strong>and</strong> vascular permeability. These results suggest<br />

an anti-arthritis activity <strong>of</strong> latex (Kumar, Roy, 2007).<br />

Latex proteins may cause allergenic responses when in contact with the skin <strong>of</strong><br />

susceptible people. These proteins are sequestered during latex coagulation (Ramos et al.,<br />

2007). Some proteins <strong>of</strong> this latex show a basic Isoelectric Point (IP) with molecular weight<br />

(MW) from 5 to 95 kDa. The most common protein has MW <strong>of</strong> 26 kDa. Among the proteins,<br />

cysteinyl proteases, quitinases <strong>and</strong> antioxidant proteins (superoxide dismutase) are found<br />

(Freitas et al., 2007). Assays showed that resolubilized proteins <strong>of</strong> coagulated latex <strong>and</strong> nontreated<br />

latex were able to stimulate immunologic activity when administered subcutaneously,<br />

developing cutaneous anaphylaxis (Ramos et al., 2006).<br />

Non dialyzed fraction <strong>of</strong> latex (NDFL) shows anti-inflammatory <strong>and</strong> analgesic activity<br />

when intraperitoneally administrated. It would be interesting to assess if NDFL has these<br />

activities by oral administration, because it does not produce allergy by this route (Ramos<br />

et al., 2007).<br />

2.2. Antinociceptive Properties<br />

Latex powder by oral administration decreased significantly abdominal contortions<br />

induced by acetic acid. Such effect was stronger when compared to pre-treatment with aspirin<br />

(Dewan, Sangraula, Kumar, 2000).

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