Shah Meet, Deshmukh Sunil Kumar, Verekar Shilpa A, Gohil Akash, Kate Abhijeet S, Rekha V, Kulkarni-Almeida Asha
NCE Research Division, Piramal Enterprises Ltd., Mumbai, India ; Vellore Institute of Technology, Vellore, India.
NCE Research Division, Piramal Enterprises Ltd., Mumbai, India.
Springerplus. 2015 Nov 19;4:706. doi: 10.1186/s40064-015-1493-6. eCollection 2015.
Mutolide an anti-inflammatory compound was isolated from the coprophilous fungus Lepidosphaeria sp. (PM0651419). The compound mitigated LPS-induced secretion of pro-inflammatory cytokines TNF-α and IL-6 from THP-1 cells as well as human peripheral blood mononuclear cells (hPBMCs). Mutolide also inhibited secretion of another pro-inflammatory cytokine IL-17 from anti-hCD3/anti-hCD28 stimulated hPBMCs. NF-κB is the major transcription factor involved in the secretion of pro-inflammatory cytokines including IL-17. Mechanistic evaluations revealed that mutolide inhibited induced NF-κB activation and translocation from cytoplasm into the nucleus. However, mutolide did not significantly affect activity of p38 MAPK enzyme, a serine/threonine kinase involved in cell cycle proliferation and cytokine secretion. These results indicate that mutolide may exert its anti-inflammatory effect via NF-κB inhibition. Oral administration of mutolide at 100 mg/kg showed significant inhibition of LPS-induced release of TNF-α from Balb/c mice in an acute model of inflammation. Our results highlight the anti-inflammatory properties of mutolide and suggest that further evaluation in a chronic model of inflammation is required to confirm the potential of mutolide as a druggable candidate for the treatment of inflammatory diseases.
Mutolide是一种抗炎化合物,从粪生真菌Lepidosphaeria sp.(PM0651419)中分离得到。该化合物可减轻LPS诱导的THP-1细胞以及人外周血单核细胞(hPBMCs)中促炎细胞因子TNF-α和IL-6的分泌。Mutolide还可抑制抗hCD3/抗hCD28刺激的hPBMCs中另一种促炎细胞因子IL-17的分泌。NF-κB是参与包括IL-17在内的促炎细胞因子分泌的主要转录因子。机制评估显示,mutolide可抑制诱导的NF-κB激活以及从细胞质向细胞核的转位。然而,mutolide对p38 MAPK酶(一种参与细胞周期增殖和细胞因子分泌的丝氨酸/苏氨酸激酶)的活性没有显著影响。这些结果表明,mutolide可能通过抑制NF-κB发挥其抗炎作用。在急性炎症模型中,以100 mg/kg的剂量口服mutolide可显著抑制Balb/c小鼠LPS诱导的TNF-α释放。我们的结果突出了mutolide的抗炎特性,并表明需要在慢性炎症模型中进一步评估,以确认mutolide作为治疗炎症性疾病的可药物化候选物的潜力。