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<title>ANTI-PLASMODIAL AND ANTI-INFLAMMATORY ACTIVITIES OF ETHANOL EXTRACT AND ETHYL ACETATE FRACTION OF Psidium guajava Linn LEAVES IN MICE AND RATS</title>
<link>http://hdl.handle.net/123456789/1970</link>
<description/>
<pubDate>Mon, 20 Apr 2026 07:10:11 GMT</pubDate>
<dc:date>2026-04-20T07:10:11Z</dc:date>
<item>
<title>ANTI-PLASMODIAL AND ANTI-INFLAMMATORY ACTIVITIES OF ETHANOL EXTRACT AND ETHYL ACETATE FRACTION OF Psidium guajava Linn LEAVES IN MICE AND RATS</title>
<link>http://hdl.handle.net/123456789/1971</link>
<description>ANTI-PLASMODIAL AND ANTI-INFLAMMATORY ACTIVITIES OF ETHANOL EXTRACT AND ETHYL ACETATE FRACTION OF Psidium guajava Linn LEAVES IN MICE AND RATS
AJAO, Mutiu Yombo
Inflammation during malaria is a determinant for the progression of plasmodial infection that&#13;
causes health burdens in humans. Emergence of parasite resistance, absence of dual&#13;
antiplasmodial and anti-inflammatory properties of current antimalarials necessitates search for&#13;
new therapeutic strategies. Psidium guajava (Pg) leaves is commonly used in ethno-medicine for&#13;
the treatment of malaria and other ailments, however, there is dearth of information of its antiinflammatory activity in malaria. This study was therefore designed to investigate the antiplasmodial and anti-inflammatory activities of Pg leaves in mice and rats.&#13;
Fresh Psidium guajava leaves were authenticated at Forest Herbarium Ibadan (FHI. 110758), airdried, pulverized, extracted with 70% ethanol (EEPg), and partitioned sequentially into n-hexane&#13;
(PgHXF), dichloromethane (PgDCF), ethyl acetate (PgEAF), and residual aqueous fractions&#13;
(PgRAF). Ninety male mice infected with Plasmodium berghei (NK65) were used for&#13;
prophylaxis, 4-Day SuppressiveTest (4-DST) and Curative Test (CT), respectively. For each test,&#13;
thirty mice were divided into five groups (n=6); 1%Tween80 (control), EEPg (100, 200,&#13;
400mg/kg) and chloroquine (10mg/kg). Anti-inflammatory activities of EEPg were investigated&#13;
in air-pouch model using thirty-six male rats allotted into six treatment groups (n=6); Normal&#13;
saline (10 mL/kg), lipopolysaccharide (100 ηg/kg), EEPg (100, 200, 400mg/kg) and&#13;
indomethacin (10 mg/kg). Cytokines (TNF-α, IL-1β) and leucocytes differentials were&#13;
determined in exudates and blood obtained from the rats. The EEPg fractions were evaluated in&#13;
mice using 4-DST. The most active fraction PgEAF was evaluated using CT with parasitemia and&#13;
Mean Survival Time (MST) determined. Blood, liver and spleen were harvested for haematology,&#13;
liver function (AST and ALT), inflammatory profiles (TNF-α, IL-6, MPO, IFN-γ, and IgG) and&#13;
markers of oxidative stress (GSH, MDA, SOD, and CAT). Histological analysis of liver and&#13;
spleen were done using standard method. Data were analysed using ANOVA at α0.05.&#13;
Chemo-suppression of EEPg in Prophylaxis (84.0, 93.5, 97.2%), 4-DST (32.5, 61.7, 77.3%), CT&#13;
(59.4, 78.6, 81.0%) was dose-dependent relative to untreated control. Pouch exudates showed&#13;
significant decrease in levels of TNF-α (30.17±2.53, 37.13±5.0, 28.605±0.59 vs&#13;
55.56±1.74pg/mg protein) and IL-1β (193.80±5.67, 158.205±0.94 vs 241.30±4.21pg/mg protein)&#13;
in EEPg compared with control. The EEPg (400mg/kg) compared with control significantly&#13;
reduced lymphocytes (35.75±4.87 vs 57.75±1.03) and neutrophils (40.0±3.63 vs 60.25±1.32)&#13;
counts. The chemo-suppression in 4-DST were PgHXF (49.3%), PgDCF (68.0%), PgEAF&#13;
(89.1%) and PgRAF (79.5%) relative to untreated control. In CT, PgEAF significantly increased&#13;
MST (20.83±1.92, 21.5±2.01, 24.83±1.6days) compared with control (10.3±0.1days). The&#13;
PgEAF (200mg/kg) significantly reduced serum AST (113.6±2.39 vs 123.4±1.07U/L), ALT&#13;
(92.62±3.05 vs 103.7±2.71U/L) and IFN-γ (73.76±1.94 vs 88.51±0.95pg/mL), and hepatic TNF-α&#13;
(38.96±1.78 vs 67.15±5.04pg/mg protein) and IL-6 (60.37±2.92 vs 94.89±0.25pg/mg protein),&#13;
respectively. Packed cell volume (25.67±0.24 vs 20.33±0.24%), haemoglobin (9.77±0.09 vs&#13;
6.63±0.09g/dL), platelet (9.33±0.47 vs 4.00±0.00 x103/µL) and serum IgG (18.54±1.01 vs&#13;
10.45±1.47pg/mL) increased significantly compared with control. PgEAF significantly reduced&#13;
hepatic MDA but increased GSH, SOD and CAT, respectively. The PgEAF prevented hepatic&#13;
and splenic injury in infected mice when compared with untreated control.&#13;
Ethanol extract of Psidium guajava leaves and its ethyl acetate fraction exhibited anti-plasmodial&#13;
and anti-inflammatory activities by parasites suppression through immune-modulation and&#13;
potentiated antioxidant activities.
</description>
<pubDate>Sat, 01 Jul 2023 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/123456789/1971</guid>
<dc:date>2023-07-01T00:00:00Z</dc:date>
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