Lemongrass Essential Oil Attenuates Perfluorooctane Sulfonate-Induced Jejunal Mucosal Injury in Rat: A Histological, Immunohistochemical, and Biochemical Study.
Amany Mohamed ShalabyAbdulfatah Mohammed AlbakkoshRania H ShalabyMohamed Ali AlabiadAmira Mostafa ElshamyMohammed AloriniFatima A JaberShereen Elsayed TawfeekPublished in: Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada (2023)
Perfluorooctane sulfonate (PFOS) has harmful impacts on various organs, including the intestine. Lemongrass essential oil (LGEO) has anti-inflammatory, anti-oxidant, antibacterial, and immunomodulatory effects. This study investigated the impact of PFOS on the mucosa of the jejunum of rats and evaluated LGEO's protective impact. Four groups of rats were created: control, LGEO (100 mg/kg/day), PFOS (5 mg/kg/day), and LGEO-PFOS group. The agents were given orally for 28 days. Oxidative stress parameters, pro-inflammatory cytokines, and caspase-3 were measured in jejunal homogenates. Rat jejunal sections were evaluated histologically (light and electron microscopic examination) and immunohistochemically [for tumor necrosis factor-α (TNF-α), Proliferating cell nuclear antigen (PCNA), cyclooxygenase-2 (COX2), and Bcl2]. PFOS significantly elevated oxidative stress, pro-inflammatory cytokines, caspase-3, and gene expression of nuclear factor kappa B (NF-kB) and inducible nitric oxide synthetase (iNOS). The disturbed architecture of jejunal villi and crypts was demonstrated. Immunohistochemically, a significant rise in TNF-α, PCNA, and COX2 and a significant decrease in Bcl2 expression were revealed compared to control group. Further ultrastructural alterations included dilated RER, mitochondria with destroyed cristae, vacuolated cytoplasm, and shrunken condensed nuclei of enterocytes. LGEO treatment significantly reduced these harmful effects. LGEO protected against PFOS-induced jejunal damage by reducing the oxidative, inflammatory, and apoptotic impacts.
Keyphrases
- oxidative stress
- nuclear factor
- anti inflammatory
- essential oil
- diabetic rats
- cell death
- induced apoptosis
- gene expression
- nitric oxide
- rheumatoid arthritis
- toll like receptor
- dna damage
- high glucose
- ischemia reperfusion injury
- single cell
- dna methylation
- poor prognosis
- nitric oxide synthase
- hydrogen peroxide
- signaling pathway
- drug induced
- mesenchymal stem cells
- cell proliferation
- bone marrow
- replacement therapy
- ulcerative colitis
- reactive oxygen species
- endoplasmic reticulum
- heat stress