اثر حفاظتی عصاره هیدروالکلی گل ساعتی (Passifloracaerulea) بر علیه سوء عملکرد کبدی القاء شده توسط کلرید کادمیوم در موشهای صحرایی نر بالغ
محورهای موضوعی : مجله پلاسما و نشانگرهای زیستیمهرداد شریعتی 1 , مهرنوش قوامی 2 , مختار مختاری 3 , سعید خاتم ساز 4
1 - گروه زیست شناسی،واحدکازرون ،دانشگاه آزاد اسلامی،کازرون،ایران
2 - گروه زیست شناسی،واحدکازرون ،دانشگاه آزاد اسلامی،کازرون،ایران
3 - گروه زیست شناسی،واحدکازرون ،دانشگاه آزاد اسلامی،کازرون،ایران
4 - گروه زیست شناسی،واحدکازرون ،دانشگاه آزاد اسلامی،کازرون،ایران
کلید واژه: سوء عملکرد کبدی, کلرید کادمیوم, گل ساعتی, موشهای صحرایی نربالغ,
چکیده مقاله :
زمینه و هدف: کلرید کادمیوم باعث ایجاد صدمه کبدی می گردد. در این مطالعه اثر حفاظتی عصاره هیدروالکلی گل ساعتی بر علیه سوء عملکرد کبدی القاء شده توسط کلرید کادمیوم در موش های صحرایی نر بالغ مورد بررسی قرارگرفت. روش کار: 54 سر موش صحرایی نربالغ نژاد ویستار به6 گروه 9 تایی تقسیم شدند. گروه کنترل،گروه شاهد1: 0.2ml/kg آب مقطر روزانه به صورت درون صفاقی به عنوان حلال دریافت کردند.گروه شاهد2: 2mg/kg کلرید کادمیوم روزانه به صورت درون صفاقی به مدت 21 روز دریافت کردند.گروه های تجربی3و2و1: 2mg/kg کلرید کادمیوم روزانه به صورت درون صفاقی به مدت 21 روز و سپس 150,300,450mg/kg عصاره هیدروالکلی بخش های هوایی گل ساعتی روزانه به صورت درون صفاقی به مدت30روز دریافت کردند. سطوح سرمی ALT,AST,ALP,GGT,LDH،آلبومین، بیلی روبین و پروتئین توتال اندازه گیری شدند. آزمایشات آسیب شناسی بافتی کبد بعد از رنگ آمیزی هماتوکسیلن وائوزین انجام شد. یافتهها: میانگین غلظت سرم ALT، ALp ،LDH ، GGT و بیلی روبین در تمام گروه های تجربی دریافت کننده کلرید کادمیوم و عصاره هیدروالکلی بخش های هوایی گل ساعتی و کلرید کادمیوم نسبت به گروه دریافت کننده کلرید کادمیوم کاهش معنی داری نشان داد. میانگین غلظت سرم AST در گروه های تجربی دریافت کننده 3و2 نسبت به گروه دریافت کننده کلرید کادمیوم کاهش معنی داری نشان داد. میانگین غلظت پروتئین توتال و آلبومین سرم در گروه های تجربی 3و2 نسبت به گروه دریافت کننده کلرید کادمیوم افزایش معنی داری نشان داد(05/0>p ). نتیجهگیری: نتایج این مطالعه نشان داد که عصاره هیدروالکلی بخش های هوایی گل ساعتی دارای اثر حفاظتی بر سوء عملکردکبدی القاء شده توسط کلرید کادمیوم در موش های صحرایی نر بالغ می باشد.
Background:Cadmium chloride causes liver injury. In this study, the protective effect of hydroalcoholic extract of Passifloracaerulea aerial parts against hepatic dysfunction induced by cadmium chloride in adult male rats was investigated. Material and Methods:Fifty-four adult male rats were divided into 6 groups of 9:control group; sham group1:received 0.2ml/kg distilled water daily intraperitoneally as solvent. Sham group2;received 2 mg/kg cadmium chloride daily intraperitoneally during 21 days; experimental groups 1, 2 and 3: received 2 mg/kg cadmium chloride daily intraperitoneally during 21 days and then the hydroalcoholic extract of Passifloracaerulea aerial parts at the doses of 150, 300, 450mg/kg intraperitoneally during 30 days . The serum levels of AST, ALT, ALP, GGT, LDH, albumin, bilirubin, and total protein were measured. The pathological examination of hepatic tissue samples were done after hematoxylin - eosin staining. Results:The mean levels of ALT, ALP, GGT, LDH and bilirubin in the all experimental groups showed a significant decrease compared to the group receiving cadmium chloride. The mean levels of AST in the experimental groups 2 and 3 showed a significant decrease compared to the group receiving cadmium chloride. The mean serum albumin and total protein concentration in experimental groups 2and 3 increased significantly compared to the group receiving cadmium chloride. In all experimental groups the hepatic tissue changes induced by cadmium chloride improved which were dose dependent (P˂0.05). Conclusion:The results of this study showed that the hydroalcoholic extract of Passifloracaerulea aerial parts had protective effects against the hepatic dysfunction induced by cadmium chloride in adult male rats.
1.Abnosi, M.H., Golami, S. (2017). Cadmium chloride treatment of rats significantly impairs membrane integrity of mesenchymal stem cells via electrolyte imbalance and lipid peroxidation, a possible explanation of Cd related osteoporosis. Iran J Basic Med Sci, 20(3); 280-287.
2.Al-Attar, A.M. (2012). Attenuating effect of Ginkgo biloba leaves extract on liver fibrosis induced by thioacetamide in mice. J Biomed Biotechnol, 2012; 761450.
3.Ali, F., Rahul., Naz, F, Jyoti, S, Siddique, Y.H. (2014). Protective effect of apigenin against N-nitroso di ethyl amine (NDEA)-induced hepatotoxicity in albino rats. Mutat Res Genet Toxicol Environ Mutagen, 767; 13-20.
4.Alkiyumi, S.S., Abdullah, M.A., Alrashdi, A.S., Salama, S.M., Abdelwahab, S.I., Hadi, A.H. (2012). Ipomoea aquatica extract shows protective action against thioacetamide-induced hepatotoxicity. Molecules, 17(5); 6146-55.
5.An, F., Yang, G., Tian, J., Wang, S. (2012). Antioxidant effects of the orientin and vitexin in Trolliuschinensis Bunge in D-galactose-aged mice. Neural Regen Res, 7(33); 2565-75.
6.Anzoise, M.L., Marrassini, C., Bach, H., Gorzalczany, S. (2016). Beneficial properties of Passifloracaerulea on experimental colitis. J Ethnopharmacol, 194; 137-145.
7.Balta, C., Herman, H., Boldura, O.M., Gasca, I., Rosu, M., Ardelean, A. (2015). Chrysin attenuates liver fibrosis and hepatic stellate cell activation through TGF-β/Smad signaling pathway. Chem Biol Interact, 240; 94-101.
8.Bataller, R., Brenner, D.A. (2005). Liver fibrosis . J Clin Invest, 115(2); 209-18.
9.Braga, A., Stein, A.C., DischkalnStolz, E., Dallegrave, E., Buffon, A., do Rego, J.C., et al. (2013). Repeated administration of an aqueous spray-dried extract of the leaves of Passifloraalata Curtis (Passifloraceae) inhibits body weight gain without altering mice behavior. J Ethnopharmacol, 145(1); 59-66.
10.Deveci, E., Deveci, S. (2011). The effects of cadmium chloride on the oesophagus of rats. Int J Morphol, 29; 678-80.
11.Dhawan, K., Kumar, S., Sharma, A. (2001). Comparative biological activity study on Passiflora caerulea and P. edulis. Fitoterapia, 72(6); 698-702.
12.Domitrović, R., Jakovac, H., Grebić, D., Milin, C., Radosević-Stasić, B. (2008). Dose- and time-dependent effects of luteolin on liver metallothioneins and metals in carbon tetrachloride-induced hepatotoxicity in mice. Biol Trace Elem Res, 126(1-3); 176-85.
13.Feliú-Hemmelmann, K., Monsalve, F., Rivera, C. (2013). Melissa officinalis and Passiflora caerulea infusion as physiological stress decreaser. Int J Clin Exp Med, 6(6); 444-51.
14.He LZMeng, Y.K., Han, Y.Z., Zhang, Z.F., Yin, P., Sang, X.X., Xiao, X.H. (2016). Protective effects of luteolin against acetaminophen-induced damage in L02 liver cells. ZhongguoZhong Yao ZaZhi, 41(22); 4234-4239.
15.Jung, U.J., Cho, Y.Y., Choi, M.S. (2016). Apigenin ameliorates dyslipidemia, hepatic steatosis and insulin resistance by modulating metabolic and transcriptional profiles in the liver of high-fat diet-induced obese mice. Nutrients, 8(5); 305.
16.Khare, P., Verma, S., Khare, N., Yadav, G. (2015). Investigation of hepatoprotective activity of passifloran epalensis. Int J Pharmacol, 9(3); 256-259.
17.Lee, W., Bork, U., Thevenod, F. (2004). Mitochondria as a target of cadmium nephrotoxocity: Induction of swelling andcytochrome C release. Toxical Mech Methods, 14(1-2); 67-71.
18.Liu, G., Zhang, Y., Liu, C., Xu, D., Zhang, R., Cheng, Y. (2014). Luteol in alleviates alcoholic liver disease induced by chronic and binge ethanol feeding in mice. J Nutr, 144(7); 1009-15.
19.Nandy, S., Paul, H.S., Kar, P.K. (2012). Determination of in vitro antioxidant activity of Passiflora nepalensis Fruit extract. Am J Pharm Tech Res, 2;3-12.
20.Patel, S.S., Saleem, T.S., Ravi, V. (2009). Passiflorain carnata Linn: A phyto pharma cological review. International Journal of Green Pharmacy, 3(4); 277-280.
21.Pushpavalli, G., Kalaiarasi, P., Veeramani, C., Pugalendi, K.V. (2010). Effect of chrysin on hepatoprotective and antioxidant status in D-galactosamine-induced hepatitis in rats. Eur J Pharmacol, 631(1-3); 36-41.
22.Raju, S.B.G., Battu, R.G., Manju latha, Y.B., Srinivas, K. (2012). Antihepatotoxic activity of smilax china roots on CCL4 induced hepatic damage in rats. Int J Pharm Pharm Sci, 4(1); 494-496.
23.Rašković, A., Gigov, S., Čapo, I., PautKusturica, M., Milijašević, B., Kojić-Damjanov, S. (2017). Antioxidative and protective actions of apigenin in a paracetamol-induced hepatotoxicity rat Model. Eur J Drug Metab Pharmacokinet, 42(5); 849-856.
24.Rehman, M.U., Ali, N., Rashid, S., Jain, T., Nafees, S., Tahir, M. (2014). Alleviation of hepatic injury by chrysin in cisplatin administered rats: probable role of oxidative and inflammatory markers. Pharmacol Rep, 66(6); 1050-9.
25.Robarts, K., Worsfold, P. (1991). Cadmium: toxicology and analysis, a review. Analyst, 116; 549-568.
26.Sakihama, Y., Cohen, M.F., Grace, S.C., Yamasaki, H. (2002). Plant phenolic antioxidant and prooxidant activities: phenolicsinduced oxidative damage mediated by metals in plants. Toxicology, 177; 67-80.
27.Sathiavelu, J., Senapathy, G.J., Devaraj, R., Namasivayam, N. (2009). Hepatoprotective effect of chrysin on prooxidant-antioxidant status during ethanol-induced toxicity in female albino rats. J Pharm Pharmacol, 61(6); 809-17.
28.Shanmugam, S., Sivaraj, D., Dos Santos Lima, B., Dos Passos Menezes, P., de Carvalho Y.M.B.G. (2017). Polyphenols rich Passiflora leschenaultii leaves modulating farnesoid x receptor and pregnane x receptor against paracetamol-induced hepatotoxicity in rats. Biomed Pharmacother, 88; 1114-1121.
29.Shanmugam, S., Thangaraj, P., Lima, B.D.S., Chandran, R., de Souza Araújo, A.A., Narain, N. (2016). Effects of luteolin and quercetin 3-β-d-glucoside identified from Passiflora subpeltata leaves against acetaminophen induced hepatotoxicity in rats. Biomed Pharmacother, 83; 1278-1285.
30.Sharma, P., Prakash, O., Shukla, A., Rajpurohit, C.S., Vasudev, P.G., Luqman, S. (2016). Structure-activity relationship studies on holy basil (Ocimum sanctum L.) based flavonoid orient in and its analogue for cytotoxic activity in liver cancer cell line HepG2. Comb Chem High Throughput Screen, 19(8); 656-666.
31.Speroni, E., Billi, R., Pellegrino, N.C., Minghetti, A. (1996). A role of chrysin in the sedative effects of Passiflora caerulea. Phytother Res, 10; 98-100.
32.Tai, M., Zhang, J., Song, S., Miao, R., Liu, S., Pang, Q. (2015). Protective effects of luteol in against acetaminophen-induced acute liver failure in mouse. Int Immunopharmacol, 27(1); 164-70.
33.Tsaroucha, A.K., Tsiaousidou, A., Ouzounidis, N., Tsalkidou, E., Lambropoulou, M., Giakoustidis, D. (2016). Intraperitoneal administration of apigenin in liver ischemia/reperfusion injury protective effects. Saudi J Gastroenterol, 22(6); 415-422.
34.Uma Devi, P., Ganasoundari, A., Vrinda, B., Srinivasan, K.K., Unnikrishnan, M.K. (2000). Radiation protection by the ocimum flavonoids orientin and vicenin: mechanisms of action. Radiat Res, 154(4): 455-60.
35.Vargas, A.J., Geremias, D.S., Provensi, G., Fornari, P.E., Reginatto, F.H., Gosmann, G. (2007). Passiflora alata and Passiflora edulis spray-dried aqueous extracts inhibit inflammation in mouse model of pleurisy. Fitoterapia, 78(2): 112-9.
36.Verma, S., Patel, S.S., Khare, P. (2014). A Study on Pharmacognostical phytochemical evaluationof leaves of Passifloran epalensis wall. Int J Pharmacol, 8(2); 170-175.
37.Wang, F., Liu, J.C., Zhou, R.J., Zhao, X., Liu, M., Ye, H. (2017). Apigenin protects against alcohol-induced liver injury in mice by regulating hepatic CYP2E1-mediated oxidative stress and PPARα-mediated lipogenic gene expression. Chem Biol Interact, 275; 171-177.
38.Wang, S.H., Shih, Y.L., Lee, C.C., Chen, W.L ., Lin, C.J., Lin, Y.S. (2009). The role of endoplasmic reticulum in cadmium-induced mesangial cell apoptosis. Chem Biol Interact, 181(1); 45-51.
39.Yang, J., Wang, X.Y., Xue,, J., Gu, Z.L., Xie, M.L. (2013). Protective effect of apigenin on mouse acute liver injury induced by acetaminophen is associated with increment of hepatic glutathione reductase activity. Food Funct, 4(6); 939-43.
40.Zhang, H., Tan, X., Yang, D., Lu, J., Liu,, B., Baiyun, R. (2017). Dietary luteol in attenuates chronic liver injury induced by mercuric chloride via the Nrf2/NF-κB/P53 signaling pathway in rats. Oncotarget, 8(25); 40982-40993.
41.Zhou, R.J., Ye, H., Wang, F., Wang, J.L., Xie, M.L. (2017). Apigenin inhibits d-galactosamine/LPS-induced liver injury through upregulation of hepatic Nrf-2 and PPARγ expressions in mice. Biochem Biophys Res Commun, 493(1); 625-630
_||_