Protective effects of scutellarin in experimental colitis in rats.
Hasan AksitDilek AksitEren AltunPublished in: Biotechnic & histochemistry : official publication of the Biological Stain Commission (2023)
Ulcerative colitis (UC) is an inflammatory bowel disease of unknown etiology for which effective treatments are lacking. Scutellarin is a flavonoid with anti-apoptotic, antioxidant and anti-inflammatory effects. We investigated the possible protective effects of scutellarin on UC induced by acetic acid in rats. We used five groups of male rats: control, scutellarin, UC, UC + scutellarin, UC + sulfasalazine. Colonic mucosal inflammation was evaluated microscopically. Malondialdehyde (MDA), superoxide dismutase (SOD) activity, total antioxidant status (TAS), nitric oxide (NO), interleukin 6 (IL-6), tumor necrosis factor-α (TNF-α) and DNA fragmentation levels were measured. Colon tissue sections were evaluated using immunohistochemistry for Bcl-2 and Bax, TUNEL staining and histopathology. Pretreatment with scutellarin significantly reduced histological damage. Scutellarin significantly reduced serum and tissue levels of MDA, NO, IL-6 and TNF-α, and increased enzymatic activity of SOD and TAS. Scutellarin suppressed apoptosis by down-regulation of Bax, reduction of DNA fragmentation and increased expression of Bcl-2. Apoptosis was increased, while antioxidant enzymes were significantly decreased; some histopathologic disorders also were seen in the UC group. Administration of scutellarin ameliorated the pathological and biochemical alterations caused by UC in rats. We found that scutellarin might be protective against UC by down-regulating pro-inflammatory cytokines and suppressing apoptosis and oxidative stress.
Keyphrases
- oxidative stress
- ulcerative colitis
- induced apoptosis
- nitric oxide
- diabetic rats
- rheumatoid arthritis
- anti inflammatory
- cell cycle arrest
- endoplasmic reticulum stress
- cell death
- ischemia reperfusion injury
- dna damage
- single molecule
- cell free
- circulating tumor
- signaling pathway
- high resolution
- atomic force microscopy
- cell proliferation
- nitric oxide synthase