Comparative evaluation of carvedilol and pitavastatin for antihyperlipidemic activity in tyloxapol-induced hyperlipidemia in Wistar rats

Md. Akbar , Hasan Ali , Md. Azizur Rahman

Intelligent Pharmacy ›› 2024, Vol. 2 ›› Issue (2) : 226 -231.

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Intelligent Pharmacy ›› 2024, Vol. 2 ›› Issue (2) : 226 -231. DOI: 10.1016/j.ipha.2023.11.009

Comparative evaluation of carvedilol and pitavastatin for antihyperlipidemic activity in tyloxapol-induced hyperlipidemia in Wistar rats

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Abstract

Aim of the study was designed to investigate the antihyperlipidemic activity of carvedilol and pitavastatin in tyloxapol-induced hyperlipidemia in Wistar rats. The rats were randomly divided into 6 groups. The vehicle control group-I received 2 mL of normal saline for eight days. The pathological control group-II received tyloxapol (400 mg/kg) on 8th day. The treated group-III received 10 mg/kg carvedilol and group-IV received 20 mg/kg carvedilol for eight days and tyloxapol (400 mg/kg) on the 8th day. The group-V received pitavastatin (0.3 mg/ kg) for eight days and tyloxapol (400 mg/kg) on the 8th day. The group-VI received carvedilol (20 mg/kg) only for eight days. After eight days of treatment, triglycerides, total cholesterol, high-density lipoprotein, very lowdensity lipoprotein, thiobarbituric acid reactive substances, and glutathione were estimated in the serum and myocardial tissues along with DNA fragmentation of the liver tissue using gel-electrophoresis. Oral administration of carvedilol to tyloxapol-induced hyperlipidemic rats normalized the changes in the above parameters in a dose dependent manner. Hence, carvedilol with pitavastatin has antihyperlipidemic activity in tyloxapol-induced hyperlipidemia in Wistar rats.

Keywords

Carvedilol / Pitavastatin / Triton WR-1339 / Tyloxapol / DNA damage / Oxidative stress

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Md. Akbar, Hasan Ali, Md. Azizur Rahman. Comparative evaluation of carvedilol and pitavastatin for antihyperlipidemic activity in tyloxapol-induced hyperlipidemia in Wistar rats. Intelligent Pharmacy, 2024, 2(2): 226-231 DOI:10.1016/j.ipha.2023.11.009

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References

[1]

AcarozU, InceS, Arslan-AcarozD, et al. Bisphenol-A induced oxidative stress, inflammatory gene expression, and metabolic and histopathological changes in male Wistar albino rats: protective role of boron. Toxicology Research. 2019;8(2):262–269.

[2]

AcarozU, InceS, Arslan-AcarozD, et al. The ameliorative effects of boron against acrylamide-induced oxidative stress, inflammatory response, and metabolic changes in rats. Food Chem Toxicol. 2018;118:745–752.

[3]

JaganjacM, Milkovic L, ZarkovicN, ZarkovicK. Oxidative stress and regeneration. Free Radic Biol Med. 2022;181:154–165.

[4]

WadheraRK, SteenDL, KhanI, Giugliano RP, FoodyJM. A review of low-density lipoprotein cholesterol, treatment strategies, and its impact on cardiovascular disease morbidity and mortality. J Clin Lipidol. 2016;10(3):472–489.

[5]

Gotto JrAM. Management of dyslipidemia. Am J Med. 2002;112(Suppl 8A):10S–18S.

[6]

GrundySM. Low-density lipoprotein, non-high-density lipoprotein, and apolipoprotein B as targets of lipid-lowering therapy. Circulation. 2002;106(20):2526–2529.

[7]

PerdomoG, Henry Dong H. Apolipoprotein D in lipid metabolism and its functional implication in atherosclerosis and aging. Aging (Albany NY). 2009;1(1):17–27.

[8]

AnsariJA, Bhandari U, PillaiKK, HaqueSE. Effect of rosuvastatin on obesity-induced cardiac oxidative stress in Wistar rats–a preliminary study. Indian J Exp Biol. 2012;50(3):216–222.

[9]

MaruyamaT, TakadaM, NishiboriY, et al. Comparison of preventive effect on cardiovascular events with different statins–the CIRCLE study. Circ J. 2011;75(8):1951–1959.

[10]

NichollsSJ, TuzcuEM, SipahiI, et al. Statins, high-density lipoprotein cholesterol, and regression of coronary atherosclerosis. JAMA. 2007;297(5):499–508.

[11]

KajinamiK, Takekoshi N, SaitoY. Pitavastatin: efficacy and safety profiles of a novel synthetic HMG-CoA reductase inhibitor. Cardiovasc Drug Rev. 2003;21(3):199–215.

[12]

RossR. Atherosclerosis-an inflammatory disease. N Engl J Med. 1999;340(2):115–126.

[13]

YueTL, Mckenna PJ, LyskoPG, et al. SB 211475, a metabolite of carvedilol, a novel antihypertensive agent, is a potent antioxidant. Eur J Pharmacol. 1994;251(2–3):237–243.

[14]

HarnafiH, CaidHS, Nour elHB, et al. Hypolipemic activity of polyphenol-rich extracts from Ocimum basilicum in Triton WR-1339-induced hyperlipidemic mice. Food Chem. 2008;108(1):205–212.

[15]

BertgesLC, Mourão Jr CA, SouzaJB, CardosoVA. Hyperlipidemia induced by triton WR1339 (tyloxapol) in wistar rats. Braz J Med Sci Health. 2011;1:32–34.

[16]

FriedmanM, ByersSO. The mechanism responsible for the hypercholesteremia induced by triton WR-1339. J Exp Med. 1953;97(1):117–130.

[17]

ZarzeckiMS, AraujoSM, BortolottoVC, de PaulaMT, JesseCR, PrigolM. Hypolipidemic action of chrysin on Triton WR-1339-induced hyperlipidemia in female C57BL/6 mice. Toxicol Rep. 2014;1:200–208.

[18]

OhPS, LeeSJ, LimKT. Hypolipidemic and antioxidative effects of the plant glycoprotein (36 kDa) from Rhus verniciflua Stokes fruit in Triton WR-1339-induced hyperlipidemic mice. BiosciBiotechnolBiochem. 2006;70(2):447–456.

[19]

LalAA, KumarT, MurthyPB, Pillai KS. Hypolipidemic effect of Coriandrum sativum L. in triton-induced hyperlipidemic rats. Indian J Exp Biol. 2004;42(9):909–912.

[20]

DemackerPN, Vos-Janssen HE, HijmansAG, van’t LaarA, Jansen AP. Measurement of high-density lipoprotein cholesterol in serum: comparison of six isolation methods combined with enzymic cholesterol analysis. Clin Chem. 1980;26(13):1780–1786.

[21]

FosterLB, DunnRT. Stable reagents for determination of serum triglycerides by a colorimetric Hantzsch condensation method. Clin Chem. 1973;19(3):338–340.

[22]

ArifM, FareedS, RahmanMA. Stress relaxant and antioxidant activities of acid glycoside from Spondias mangifera fruit against physically and chemically challenged albino mice. J Pharm BioAllied Sci. 2016;8:58–63.

[23]

TahirM, RahmanMA, KhushtarM. Gastroprotective effect of Hyssopus officinalis L. leaves via reduction of oxidative stress in indomethacin-induced gastric ulcer in experimental rats. Drug Chem Toxicol. 2022;45(1):291–300.

[24]

TariqueM, Siddiqui HH, KhushtarM, RahmanMA. Protective effect of hydroalcoholic extract of Ruta graveolens Linn. leaves on indomethacin and pylorus ligation-induced gastric ulcer in rats. J Ayurveda Integr Med. 2016;7:38–43.

[25]

ZahidM, ArifM, RahmanMA, Mujahid M. Hepatoprotective and antioxidant activities of Annona squamosa seed extract against alcohol-induced liver injury in Sprague Dawley rats. Drug Chem Toxicol. 2020;43(6):588–594.

[26]

BursteinM, Scholnick HR, MorfinR. Rapid method for the isolation of lipoproteins from human serum by precipitation with polyanions. J Lipid Res. 1970;11(6):583–595.

[27]

FriedewaldWT, LevyRI, FredricksonDS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972;18(6):499–502.

[28]

OhkawaH, OhishiN, YagiK. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95(2):351–358.

[29]

KhushtarM, AhmadA, RahmanMA. Gastroprotective effect of hydro-alcoholic extract of Polygonum bistorta Linn root in indomethacin-induced gastric ulcers in Sprague Dawley rats. Indian Journal of Pharmaceutical Education and Research. 2018;52(4):618–625.

[30]

AlamJ, Mujahid M, JahanY, BaggaP, RahmanMA. Hepatoprotective potential of ethanolic extract of Aquilaria agallocha leaves against paracetamol induced hepatotoxicity in SD rats. Journal of Traditional and Complementary Medicine. 2017;7(1):9–13.

[31]

UsmaniA, Mujahid MD, KhushtarM, SiddiquiHH, RahmanMA. Hepatoprotective effect of Anacyclus pyrethrum Linn against antitubercular drugs-induced hepatotoxicity in SD rats. J Compl Integr Med. 2016;13(3):295–300.

[32]

EramS, Mujahid M, BaggaP, AhsanF, RahmanMA. Hepatoprotective evaluation of Galanga (Alpinia officinarum) rhizome extract against antitubercular drugs induced hepatotoxicity in rats. J Herbs, Spices, Med Plants. 2020;26(2):113–125.

[33]

SaidurrahmanM, Mujahid M, SiddiquiMA, AlsuwaytB, RahmanMA. Evaluation of hepatoprotective activity of ethanolic extract of Pterocarpus marsupium Roxb. leaves against paracetamol-induced liver damage via reduction of oxidative stress. Phytomedicine. 2022;2(3):100311.

[34]

UrfiMK, Mujahid M, Badruddeen RahmanMA, RahmanMA. The role of Tamarix gallica leaves extract in liver injury induced by rifampicin plus isoniazid in SD rats. J Diet Suppl. 2018;15(1):24–33.

[35]

MeenaSZ, RahmanMA, BaggaP, Mujahid M. Hepatoprotective activity of Tamarindus indica Linn stem bark ethanolic extract against hepatic damage induced by co-administration of antitubercular drugs isoniazid and rifampicin in Sprague Dawley rats. J Basic Clin Physiol Pharmacol. 2018;30(1):131–137.

[36]

CarlbergI, Mannervik B. Purification and characterization of the flavoenzyme glutathione reductase from rat liver. J Biol Chem. 1975;250(14):5475–5480.

[37]

LowryOH, Rosebrough NJ, FarrAL, RandallRJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193(1):265–275.

[38]

IqbalSS, Mujahid M, KashifSM, et al. Protection of hepatotoxicity using Spondias pinnata by prevention of ethanol-induced oxidative stress, DNA-damage and altered biochemical markers in Wistar rat. Integrative Medicine Research. 2016;5(4):267–275.

[39]

LingH, LouY. Total flavones from Elsholtziablanda reduce infarct size during acute myocardial ischemia by inhibiting myocardial apoptosis in rats. J Ethnopharmacol. 2005;101(1–3):169–175.

[40]

FeuersteinGZ, FisherM, NunnartJ, Ruffolo JrRR. Carvedilol inhibits aortic lipid deposition in the hypercholesterolemic rat. Pharmacology. 1997;54(1):24–32.

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