Abstract
Phytol (PHY) is an acyclic natural diterpene alcohol and a chlorophyll constituent that exhibits several pharmacological effects, such as anticancer, antioxidant, and antimicrobial. Here, we aimed to assess the PHY anti-inflammatory effect in vitro and in vivo, and to deepen knowledge on the possible mechanism of action. For this purpose, egg albumin (in vitro) test was performed by using acetyl salicylic acid (ASA) as a standard nonsteroidal anti-inflammatory drugs (NSAID). For in vivo test, male Wistar albino rats were treated (intraperitoneally) with 100 mg/kg of PHY and/or standard NSAIDs ASA (100 mg/kg) and diclofenac sodium (Diclo-Na, 10 mg/kg) to evaluate the combined effect of PHY in formalin-induced paw edema model. Furthermore, an in silico (CADD) study was accomplished to assess the effect of PHY against cyclooxygenase (COX)-1 and 2 enzymes, nuclear factor kappa B (NF-κB), and interleukin-1β (IL-1β). Results revealed that PHY exhibits dose-dependent anti-inflammatory effect using the egg albumin method. PHY (100 mg/kg) co-treated with ASA and/or Diclo-Na reduced paw edema better than PHY alone or NSAIDs individual groups. Computational study showed that PHY efficiently interacts with COX-1 and 2, NF-κB, and IL-1β. In conclusion, PHY exhibits anti-inflammatory activity, possibly via COX-1 and 2, NF-κB, and IL-1β dependent pathways.
Highlights
Phytol (PHY) is an acyclic natural diterpene alcohol and a constituent of chlorophyll abundantly found in nature [1]
COX-2 pathways transcription and induction are activated by cytokines and TNF, triggering the central mechanisms that act via the transcription factors such nuclear factor kappa B (NFκB) and signal transducer and activator of transcription (STAT-3) [8,9]
PHY when co-administered with acetyl salicylic acid (ASA) or Diclo-Na was found to be more potent in reducing paw edema than PHY, ASA, and Diclo-Na groups
Summary
Phytol (PHY) is an acyclic natural diterpene alcohol and a constituent of chlorophyll abundantly found in nature [1]. Research findings have shown that several inflammatory mediators, among them interleukin 1 beta (IL1β) and tumor necrosis factor alpha (TNF-α), are involved in the nociceptive response to chemical stimulus in experimental animals [3,4] In this context, prostaglandins synthesis displays a key role in both inflammatory and febrile response to endogenous (e.g., cytokines) or exogenous (e.g., lipopolysaccharide) pyrogens [5]. Cyclooxygenase (COX) enzymes are involved in inflammation- and pain-related symptoms [6] Along this line, nonsteroidal anti-inflammatory drugs (NSAIDs), such as aspirin (acetyl salicylic acid, ASA) and diclofenac (e.g., Diclofenac sodium, Diclo-Na) exert their effect by inhibiting the COX activity. Results of this study may have some pharmacological implications as to the use of PHY as anti-inflammatory
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