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BUKU ABSTRAK - Universiti Putra Malaysia

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Mesenchymal Stem Cells Modulate Neutrophils’ Respiratory Burst Activity: An<br />

Impact on Chronic Inflammatory Diseases<br />

Dr. Rajesh Ramasamy<br />

Maryam Maqbool and Sharmili Vidyadaran<br />

Faculty of Medicine and Health Sciences, University <strong>Putra</strong> <strong>Malaysia</strong>,<br />

43400 UPM Serdang, Selangor, <strong>Malaysia</strong>.<br />

+603-8947 2377; r.rajesh@medic.upm.edu.my<br />

Neutrophils or polymorphonuclear leucocytes (PMN) are major cell type that constitutes innate immunity.<br />

They comprise approximately 50-70% of leucocytes and predominate in eliminating pathogens that induce acute<br />

inflammation. In bone marrow, mesenchymal stem cells (MSC) protect neutrophils from apoptosis, preserving<br />

their effector functions and preventing excessive or inappropriate activation of the oxidative burst. PMN use<br />

oxygen-dependent mechanisms that involve the production of reactive oxygen species (ROS) and reactive<br />

nitrogen species (RNS). Generation of ROS from stimulated neutrophils is thought to play an important role<br />

in host defence and tissue damage. Therefore the current study, we evaluate the effects of MSC on neutrophils<br />

respiratory burst activity. Chemiluminescence and Griess assays are widely used as sensitive and accurate<br />

measurements to assess the neutrophils’ reactive oxygen and nitrogen species production. The effect of MSC on<br />

generation of ROS by neutrophils was evaluated at different time points in the present of absence of MSC. Our<br />

study shows that MSC at all ratios in 24 and 48 hours inhibit the ROS production in chemiluminescence assay.<br />

Furthermore, in Griess assay, it was observed that at 24 and 48 hours, MSC inhibit the nitric oxide production.<br />

Our results indicate that MSC could be potentially serve as therapy to dampen neutrophils respiratory burst during<br />

an exaggerated neutrophils responses whereby the over production of ROS and RNS can cause harmful effects<br />

to other neighbouring cells and tissue. MSC can be also proposed as a component in treating chronic neutrophils<br />

responses such as arthritis and other chronic inflammatory diseases.<br />

Keywords: Neutrophil, respiratory burst, mesenchymal stem cells<br />

Anti-inflammatory and Anti-pyretic Effects of Hexane Fraction of Ardisia crispa<br />

Dr. Roslida Abd. Hamid<br />

Lau Moi Fong, Sabrina Sukardi and Muhammad Nazrul Hakim Abdullah<br />

Faculty of Medicine and Health Sciences, University <strong>Putra</strong> <strong>Malaysia</strong>,<br />

43400 UPM Serdang, Selangor, <strong>Malaysia</strong>.<br />

+603-8947 2341; roslida@medic.upm.edu.my<br />

Hexane fraction of Ardisia crispa root (ACHE) was used to investigate its anti-inflammatory and anti-pyretic<br />

activities in this study. For anti-inflammatory activity, 12-O-tetradecanoylphorbol-13-acetate (TPA) was applied<br />

to the ear of mice to induce oedema and treated with 0.5,1 and 2mg/ear of ACHE topically. In cotton-pellet<br />

granuloma test, treated groups have received 3, 10, 30 and 100mg/kg of hexane extract administered orally for<br />

seven days. For antipyretic activity, brewer’s yeast was injected in mice to induce fever and later, ACHE at dose<br />

ranging from 10 to 300 mg/kg was administered to the rats orally. The results exhibited that 1 and 2mg/ear of<br />

ACHE produced significant suppression by 19.9% and 20.2% respectively. The lowest dose of ACHE showed no<br />

significant effect when compared with control. Results showed that ACHE showed significant anti-pyretic effect<br />

at all doses (10, 30, 100 and 300 mg/kg). At 30, 100 and 300mg/kg, ACHE even exhibited higher efficacy when<br />

compared with 100 mg/kg acetaminophen. ACHE also elicited a significant (P

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