Rutin attenuates intestinal toxicity induced by Methotrexate linked with anti-oxidative and anti-inflammatory effects

Methotrexate (MTX) is an antagonist of folic acid [1]. MTX competitively inhibits the dihydrofolate reductase (DHFR) enzyme, which participates in the synthesis of folic acid and is requisite for denovo synthesis of purine [1]. Subsequently, MTX is used as an antimetabolite in cancer chemotherapy. Additionally, MTX also plays a crucial role in the treatment of range of diseases including lymphocytic leukemia, non- hodgkin’s lymphoma, osteosarcoma, head neck cancer, and mammary gland tumors [2]. Moreover, MTX is also intervened for treatment of other disease conditions such as rheumatoid arthritis and refractory inflammatory disease [3]. Notwithstanding, the adequacy of MTX is restrained by its relentless and toxic sequel, including intestinal injury, enterocolitis, cardiotoxicity, nephrotoxicity and hepatotoxicity. The MTX administration deteriorates barrier function of the mucosa, resulting in bacterial translocation and inflammation [4]. The intestinal damage include conspicuous morphological injuries in the small intestine, mucosal damage and compromised mucosal barrier function [5]. Pharmacodynamically MTX treatment results in malabsorption, diarrhea, weight loss and disrupted chemotherapy [6]. The mechanism beneath the gastrointestinal toxicity of MTX is below par understood and therefore; the cancer chemotherapy is customarily accompanied by symptomatic therapies such as antibiotic and anti-diarrheal drugs.

Flavonoids are ubiquitous polyphenolic compounds with wide distribution in herbs, vegetables, fruits and beverages [7]. Flavonoids are proclaimed to have antioxidant, anti-inflammatory, anticancer and gastroprotective properties. Flavonoids are reputed to have significant reactive oxygen species (ROS) scavenging along with diminishing effects on arachidonic acid (AA) cascade bagged by dual inhibition of cyclooxygenase (COX) and lipoxygenase (LOX) pathway as well. Rutin is a flavone glycoside, extensively found in black tea, apple skin peel and buckwheat. Antecedently, rutin has been reputed to have significant anti-inflammatory, antioxidant, mucus protective and antiulcer properties through decreased histamine synthesis and increased production of cytoprotective prostaglandins and many more [8, 9]. Rutin has also been reported to strengthen of the capillaries of blood vessels which are the result of its high ROS scavenging activity and antioxidant capacity [10, 11]. In addition, aglycone part of rutin could block both COX and LOX pathway at high concentration, furthermore the lipoxygenase pathway is primarily the target of inflammation inhibition at low concentration of rutin [10, 12].

Considering the role of oxidative stress in MTX associated intestinal damage and unchallenged ROS scavenging activity of rutin, it is hypothesized that rutin can ameliorate the oxidative damage induced by MTX and can be set forth as an adjuvant in MTX chemotherapeutic regimens. Henceforth, the current study was carried out to validate the above hypothesis.

MTX is an antimetabolite and antifolate agent which competitively inhibits the binding of folic acid to its cognate enzyme DHFR [22]. MTX was originally refined and continues to be used for chemotherapy either alone or in combination with other agents [23]. The use of MTX is often times assigned with intestinal toxicities along with cardiotoxicity, nephrotoxicity and hepatotoxicity [24, 25]. To minimize the side effects in patients undergoing chemotherapy, it is important to curtail mucosal damage and prompt up the tissue repair. The antecedent studies have accumulated the concurrence of ROS in the pathogenesis of MTX toxicity. Various research groups had exploited the pathway for ROS to counteract such toxicities, and the same was contemplated in the present experiment through concomitant therapy of rutin [26].

Treatment with rutin evidenced a dose dependent preservation against the intestinal toxicity when ascertained through physiological parameters. The rutin treatment manifested compelling rise in intestinal pH with decrease in the total and free acidity. The CMDI score in the toxic control was also scaled down momentously by rutin in a dose dependent manner suggesting a positive modulation by rutin. Prima facie the rutin was observed to have marked assurance against the MTX induced intestinal toxicity, and the same could be accredited to the antisecretory potential of rutin [17].

To further investigate, we figured out the effect of rutin on enzymatic antioxidant defense along with markers of lipids and proteins peroxidation. Increased production of MDA and protein carbonyl was illustrated in the MTX treated group, which is in corroboration with the previous studies [27, 28]. Body cells and tissues are in endless threat by the free radicals, which are propagated either through normal oxygen metabolism or induced by exogenous damage (MTX in present case) [29‐31]. The mechanism/s or sequence/s of events associated with the free radicals bracketed cellular dysfunction is not fully understood, but lipid and protein peroxidation are the important markers for this [32]. The protein and lipid adjustment elected by the direct oxidative stress on amino acid residues and phospholipids can link to the formation of carbonyl derivatives and MDA, which are extensively used as a marker for oxidative stress [21]. In the present experimental condition, MTX proclaimed significant increase in the levels of protein carbonyl along with MDA, and rutin subsequently helped to restore the same in a dose dependent manner.

GSH plays an important role in protecting tissues from per oxidative attack and is perceived as a first line defense against the ROS attack. The previous report suggests that the tissue GSH levels are subsided as a repercussion of peroxidative attack [33]. Nonetheless, we contemplated marked increase in the tissue GSH levels after MTX toxicity, and the same could be attributed to the marked up biogenesis of GSH as a feedback, in consequence to overwhelming ROS generation. Rutin was contemplated to restore the GSH levels in dose dependent manner and the same could be attributed to decrease in oxidative stress. The above discussion clearly acclaims the participation of ROS in MTX toxicity and its affray by rutin.

The SOD and catalase integrate a major supportive team of defense against ROS. SOD catalyses the scavenging of the superoxide radical leading to the formation of hydrogen peroxide, which is afterwards catabolised by catalase to water and molecular oxygen. Both the enzymes work in tandem to affray the ROS [34, 35]. In the present experiment, a significant decrease in the enzymatic activity of SOD and catalase was prevalent in the MTX treated group, which could be accredited to the up turned oxidative stress. Rutin implemented a conspicuous protection against the MTX induced intestinal toxicity in a dose dependent manner. After going through the biological makers of the oxidative stress, the authors are in a strong opinion that rutin can flapdown the deleterious effects associated with the MTX chemotherapy.

The precedent studies have also suggested the immune dysfunction coupled with the MTX toxicity [36]. Henceforth, we in quested the levels of anti-inflammatory (IL-10) and immunoregulatory (IL-2 and IL-4) cytokines after the concomitant administration of rutin. The IL-2 and IL-4 are the signaling molecules in the immune system. The IL-2 regulates the activity of white blood cells and IL-4 participates in the differentiation of naive helper T cells (Tho cells) to Th2 cells [37]. Both IL-2 and IL-4 are produced either normally or as a consequence of activation by T cells during an immune response [38, 39]. We ascertained a momentous increase in the activity of IL-2 and IL-4 after the MTX therapy and are of the opinion, that the utmost immunocompromised state after MTX could have actuated a feedback mechanism. Nonetheless, the levels of IL-2 and IL-4 were somewhat restored after the rutin administration, implying the redeemed immunological status. When observed for IL-10 (anti-inflammatory cytokine) the MTX administration perceived momentous decrease and the same was restored to normal after low dose rutin. The MTX administration was clearly suggestive of immunocompromised status with pronounced inflammation and the same was restored to normal with subsequent administration of rutin.

The free radical scavenging activity of rutin and its metabolite quercetin is a well studied phenomenon. Both rutin and quercetin can suppress the free radical generation at three stages: formation of superoxide ion, generation of hydroxyl (cyprohydroxy) radical in fenton reaction and formation of lipid peroxy radicals [40]. Nonetheless, the mechanism beneath the anti-inflammatory potential of rutin is unexplored/not reported until now and to inquest the same we enumerated the effect of rutin on COX and LOX enzymes in vitro. The results helped us to derive that; rutin by inhibiting the COX/LOX pathway of AA metabolism can curb the inflammatory reaction as conceded with MTX. It would be pertinent to mention that dual inhibitors of AA metabolism have manifested an excellent preclinical gastrointestinal pharmacological safety (Argentieri et al., 1994). Moreover, recent findings from phase II and III studies of the clinical development of licofelone (dual inhibitor of AA metabolism) indicate that licofelone has an excellent gastrointestinal safety, which is better than conventional NSAIDs [41]. It is to be noted that rutin when given independently could afford significant rise in the intestinal pH, total acidity and free acidity, which could be accredited to the formation of polar metabolites of rutin in the intestine [42]. It is to be noted further that MTX is excreted (90 %) unchanged in the urine through combination of glomerular filtration and active tubular secretion and changes/decrease in renal excretion can delay elimination and lead to severe myelosuppression [43]. MTX is often prescribed with biocarbonate to maintain the pH of above 6.5 and subsequent excretion. The increase in intestinal pH by rutin therefore may afford a facilitated excretion of MTX and thus could eliminate the use of biocarbonates in therapeutic regimes along with chances of myelosuppression.

Henceforth, one can derive that the rutin exhibits significant physiological, biochemical and immunological protection against MTX induced intestinal toxicity in a dose dependent manner and can be advocated as an adjuvant therapy in MTX chemotherapy to countervail the deleterious effects. The free radical scavenging, immunoregulatory and dual inhibitory potential of AA metabolism could be considered as the possible mechanisms for the actions of rutin as observed in the present experiment.