Flax seed oil and flax seed meal reduce the formation of aberrant crypt foci (ACF) in azoxymethane-induced colon cancer in Fisher 344 male rats

2007 ◽  
Vol 45 (1) ◽  
pp. 153-159 ◽  
Author(s):  
D. Williams ◽  
M. Verghese ◽  
L.T. Walker ◽  
J. Boateng ◽  
L. Shackelford ◽  
...  
2008 ◽  
Vol 4 (2) ◽  
pp. 28-40 ◽  
Author(s):  
D.S. Williams ◽  
M. Verghese ◽  
L.T. Walker ◽  
J. Boateng ◽  
L.A. Shackelfor ◽  
...  
Keyword(s):  
Seed Oil ◽  

2008 ◽  
Vol 8 (2) ◽  
pp. 410-415 ◽  
Author(s):  
A. Clisby ◽  
M. Verghese ◽  
E. Cebert ◽  
L.T. Walker ◽  
R. Field ◽  
...  

2020 ◽  
Vol 20 (17) ◽  
pp. 2041-2052
Author(s):  
Zahra Sahebi ◽  
Mozhgan Emtyazjoo ◽  
Pargol G. Mostafavi ◽  
Shahin Bonakdar

Background and Purpose: This study subjected a rat model to the extracts of muscle and shell tissues from Portunus segnis to assess their therapeutic effects on the HT-29 colon cancer cells as well as on colonic Aberrant Crypt Foci (ACF) induced by Azoxymethane (AOM). Methods: The cell line was exposed to the extracts to compare the cytotoxicity of hexane, butanol, ethyl acetate, and water extract of muscle and ethanolic extract of the shell. Male rats (n=40) were assigned into control, positive, negative, and treatment groups. The animals were injected with AOM, except the control group, and then exposed to 250 and 500mg/kg of the crude extracts. Immunohistochemical localization of Bax and Bcl-2, as well as ACF and antioxidant enzymes, were evaluated in the rat colon. Results: The butanolic muscle extract and ethanolic shell one demonstrated an IC50 of 9.02±0.19μg/ml and 20.23±0.27μg/ml towards the cell line, respectively. Dietary exposure inhibited the ACF formation and crypt multiplicity in the colon compared to the cancer control group. The activity of SOD and CAT increased, while that of MDA decreased. The expression of Bax and Bcl-2 increased and decreased, respectively. Conclusion: Taken together, the results show that both extractions were suggested to be suppressive to AOMinduced colon cancer.


2020 ◽  
Author(s):  
Fatemeh Hajiaghaalipour ◽  
Elham Bagheri ◽  
Elham Rouhollahi ◽  
Nur'ain Salehen ◽  
Mahmood Ameen Abdulla

Abstract Background Tea (Camellia sinensis) is one of the most consumed beverages in the world. White tea is an unfermented tea made from young tea leaves or unopened buds. Methods The in vitro antiproliferation assay and in vivo Chemopreventive effects of white tea extract (WTE) using azoxymethane (AOM) induced aberrant crypt foci (ACF) in rats was assessed. Twenty-four adult male rats were injected 15 mg/kg body weight AOM subcutaneously once a week for two weeks and then were divided randomly into four groups. Group I (Cancer control), Group II (treated whit 200 mg/kg white tea extract), Group III (treated whit 400 mg/kg white tea extract) and group IV (35 mg/kg body weight 5-fluorouracil as reference control). On the last day of the experiment, the animals were euthanized using an overdose of ketamine and xylazine and the colon tissue was collected. The colon tissues were evaluated grossly and histopathologically for aberrant crypt foci (ACF). Prior to the cancer studies, the acute toxicity test was performed to demonstrate the safety usage of the extract. Results The antiproliferative activity of the extract was observed in HT-29 and HCT 116 colon cancer cells. The ACF score was significantly reduced following the white tea extract treatment in a dose-dependent manner. Furthermore, the acute toxicity study indicated that there were no nephrotoxic and hepatotoxic effects or any serum biochemical changes in the rats that were orally administered with 2000 mg/kg body weight of the extract. Conclusions This study suggested the the potential of white tea as a chemopreventative agent through inhibition of Azoxymethane-induced Colonic Aberrant Crypt Foci Formation in the male Sprague-Dawley rats.


2021 ◽  
pp. 29-31
Author(s):  
Seval Kaya ◽  
Yusuf Nergiz ◽  
Firat Asir

In this study, it was aimed to investigate the protective effect of black seed oil against testicular tissue damage in diabetic rats. A total of 18 male rats were divided into 3 groups, including 6 rats in each group.Groups; control (n=6), diabetes (n=6), diabetes + black seed oil (n=6). A single dose of 45 mg / kg streptozocine (STZ) was injected intraperitoneally to induce diabetes. Diabetes + Black seed oil group: For 56 days, 2.5 ml / kg of black seed oil was administered orally to rats.The rats were sacriced at the end of 56 days. Testicular tissues were taken for routine parafn tissue processing for histopathological examination. Parafn sections were stained with Hematoxylin-Eosin and PAS and examined under a light microscope. Atrophy and degeneration were observed in the seminiferous tubules of diabetic group. Histology of black seed oil group sections were similar to that of control group. A signicant difference was found between the black seed oil group and the diabetes group in terms of blood glucose values. As a result, we think that Black Seed Oil ameliorates to the tissue damage caused by diabetes and the decrease in blood sugar value.


2020 ◽  
Vol 57 (3) ◽  
Author(s):  
Sahar Hassan Orabi ◽  
Sherif Mohamed Shawky

The current study focused on investigating the renoprotective effects of grape seed oil (GSO) against hexavalent chromium (Cr (VI))-induced nephrotoxicity. A total of 40 male rats were randomly divided into four groups: group I served as the control group, group II received 1000 mg/L potassium dichromate (353.5 mg/L Cr(VI)) in drinking water for 12 weeks, group III received 3.7 g/kg body weight/day GSO orally for 12 weeks, and group IV received GSO together with potassium dichromate for 12 weeks. Cr(VI) significantly increased serum levels of urea, creatinine, potassium and glucose. In addition, Cr(VI) increased MDA levels and induced renal tissue damage and DNA damage. On the other hand, Cr(VI) decreased serum levels of sodium and antioxidant defence system [reduced glutathione (GSH) and catalase (CAT)]. However, treatment with GSO prevented elevation levels of serum urea, creatinine, potassium and glucose. In addition, GSO enhanced sodium level, renal tissue antioxidant defense system due to its curative effect ameliorated particularly oxidative stress, renal tissue and DNA damage. In conclusion, these results demonstrate that GSO is a promising nephroprotective agent against Cr(VI)-induced nephrotoxicity.Key words: grape seed oil; hexavalent chromium; nephrotoxicity; DNA damage BLAŽILNI UČINKI OLJA GROZDNIH PEŠK PRI TOKSIČNI OBREMENITVI LEDVIC TER VPLIV NA OKSIDATIVNI STRES PODGAN, POVZROČEN S KROMOM Povzetek: Študija je bila osredotočena na proučevanje zaščitnih učinkov olja grozdnih pešk (GSO) pri toksični obremenitvi ledvic, povzročeni s heksavalentnim kromom (Cr (VI)). Štirideset samcev podgan je bilo naključno razdeljenih v štiri skupine: skupina I - kontrolna skupina, skupina II, ki je v pitni vodi 12 tednov prejemala 1000 mg/L kalijevega dikromata (353,5 mg/L Cr (VI)), skupina III, ki je peroralno 12 tednov prejemala 3,7 g/kg telesne mase/dan GSO ter skupina IV, ki je 12 tednov prejemala GSO skupaj s kalijevim dikromatom. Cr(VI) je znatno zvišal serumske ravni sečnine, kreatinina, kalija in glukoze v serumu. Poleg tega je Cr(VI) zvišal raven MDA in povzročil poškodbe ledvičnega tkiva in poškodbe DNK. Po drugi strani je Cr(VI) znižal serumsko raven natrija in antioksidativnega obrambnega sistema, zmanjšal raven glutationske peroksidaze in katalaze. Dodajanje GSO poskusnim živalim je preprečilo zvišanje ravni sečnine v serumu, kreatinina, kalija, natrija in glukoze. Poleg tega je GSO izboljšal obrambni sistem antioksidantov ledvičnega tkiva. Zaradi svojega zdravilnega učinka je izboljšal zlasti oksidativni stres, poškodbe ledvičnega tkiva in DNK. Rezultati kažejo, da je GSO obetavno zaščitno sredstvo za ledvica pri toksični obremenitvi, povzročeni s Cr(VI).Ključne besede: olje grozdnih pešk; heksavalentni krom; nefrotoksičnost; poškodba DNK


2010 ◽  
Vol 24 (S1) ◽  
Author(s):  
Aaron Mehrer ◽  
Afrin Kamal ◽  
Betty L Herndon ◽  
Eugene Fibuch ◽  
Tim Quinn ◽  
...  
Keyword(s):  
Seed Oil ◽  

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
V. Ganga Prasad ◽  
Shishir Kawade ◽  
B. S. Jayashree ◽  
Neetinkumar D. Reddy ◽  
Albi Francis ◽  
...  

The aim of the present study was to evaluate the antitumor potential of iminoflavones inin vitroandin vivoanticancer models. Preliminary screening in various cancer cell lines revealed four potential iminoflavones out of which IMF-8 was taken based on its activity against colon cancer cells. This was further confirmed by observing the nuclear changes in the cells by AO/EB and Hoechst 33342 staining studies.In vivoactivity was assessed by dimethyl hydrazine-(DMH-) induced colon cancer model in rats. Animals were administered DMH (20 mg/kg, b.w. for 10 weeks and 30 mg/kg b.w.,i.p.for 10 weeks) and were supplemented with (IMF-8) iminoflavone-8 (200 mg/kg,p.o.for 14 days). Results showed that DMH induced 100% aberrant crypt foci (ACF) and polyps which were significantly reduced in the IMF-8 treated group. IMF-8 significantly increased the catalase and GSH levels whereas it reduced the TNF-αand IL-6 levels markedly which suggests the antioxidative and anti-inflammatory actions of flavonoids present in IMF-8. The histopathological images of the IMF-8 treated colon showed no signs of mucosal crypt abscess. These findings suggest that the semi-synthetic iminoflavones, IMF-8, effectively inhibit DMH-induced ACFs and colonic crypts by alleviating the oxidative stress and suppressing the inflammation.


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