Home Ameliorative effects of Annona muricata Linn. (Annonaceae) against potassium dichromate-induced hypertension in vivo: involvement of Kim-1/p38 MAPK/Nrf2 signaling
Article
Licensed
Unlicensed Requires Authentication

Ameliorative effects of Annona muricata Linn. (Annonaceae) against potassium dichromate-induced hypertension in vivo: involvement of Kim-1/p38 MAPK/Nrf2 signaling

  • Olufunke Eunice Ola-Davies , Ademola Adetokunbo Oyagbemi EMAIL logo , Temidayo Olutayo Omobowale , Israel Akande and Anofi Ashafa
Published/Copyright: May 3, 2019

Abstract

Background

Recently, the incidences of hypertension and environmental pollution have increased significantly. This study investigates the antihypertensive effect of Annona muricata extract against K2Cr2O7-induced hypertension.

Methods

Fifty rats were used for this study, which were divided into five groups of 10 rats each. Rats in Group A received normal saline, and those in Groups B, C, D, and E were treated with A. muricata extract alone at 250 mg/kg, K2Cr2O7 at 30 mg/kg, pretreated with the extract at 250 mg/kg, and pretreated with gallic acid at 60 mg/kg for 14 days, respectively, and thereafter administered with a single intraperitoneal injection of K2Cr2O7 at 30 mg/kg.

Results

Administration of K2Cr2O7 significantly increased systolic, diastolic, and mean arterial pressure and caused prolonged QT and QTc intervals. Further, pretreatment with the extract at 250 mg/kg and gallic acid at 60 mg/kg significantly reduced high blood pressure to near-normal values. K2Cr2O7 intoxication led to significant increases in serum advanced oxidative protein products, myeloperoxidase, and xanthine oxidase, while serum nitric oxide (NO) also reduced significantly. Immunohistochemistry of the renal kidney injury molecule (Kim-1) and p38 MAPK showed increased expressions following the administration of K2Cr2O7 together with the downregulation of nuclear factor erythroid 2-related factor 2 (Nrf2). Pretreatment with the extract at 250 mg/kg and gallic acid at 60 mg/kg also increased the expressions of Nrf2 and downregulated Kim-1 and p38.

Conclusion

Together, we found that pretreatment with the extract at 250 mg/kg and gallic acid at 60 mg/kg normalized the blood pressure, reduced the markers of oxidative stress, and improved the antioxidant defense system and serum NO bioavailability.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

[1] Moghadamtousi SZ, Fadaeinasab M, Nikzad S, Mohan G, Ali HM, Kadir HA. Annona muricata (Annonaceae): a review of its traditional uses, isolated acetogenins and biological activities. Int J Mol Sci 2015;16:15625–58.10.3390/ijms160715625Search in Google Scholar

[2] Mishra S, Ahmad S, Kumar N, Sharma BK. Annona muricata (the cancer killer): a review. Glob J Pharm Res 2013;2:1613–8.Search in Google Scholar

[3] Adewole SO, Caxton-Martins EA. Morphological changes and hypoglycemic effects of Annona muricata Linn. (Annonaceae) leaf aqueous extract on pancreatic B-cells of streptozotocin-treated diabetic rats. Afr J Biomed Res 2006;9:173–87.10.4314/ajbr.v9i3.48903Search in Google Scholar

[4] Jaramillo-Flores M, Hernandez-Sanchez H. Thermal diffusivity of soursop (Annona muricataL.) pulp. J Food Eng 2000;46:139–43.10.1016/S0260-8774(00)00074-1Search in Google Scholar

[5] Tundis R, Xiao J, Loizzo MR. Annona species (Annonaceae): a rich source of potential antitumor agents? Ann N Y Acad Sci 2017;1398:30–6.10.1111/nyas.13339Search in Google Scholar PubMed

[6] Md Roduan MR, Hamid RA, Sulaiman H, Mohtarrudin N. Annona muricata leaves extracts prevent DMBA/TPA-induced skin tumorigenesis via modulating antioxidants enzymes system in ICR mice. Biomed Pharmacother 2017;94:481–8.10.1016/j.biopha.2017.07.133Search in Google Scholar PubMed

[7] Acésio NO, Carrijo GS, Batista TH, Damasceno JL, Côrrea MB, Tozatti MG, et al. Assessment of the antioxidant, cytotoxic, and genotoxic potential of the Annona muricata leaves and their influence on genomic stability. J Toxicol Environ Health A 2017;80:1290–300.10.1080/15287394.2017.1377653Search in Google Scholar PubMed

[8] Agu KC, Okolie PN. Proximate composition, phytochemical analysis, and in vitro antioxidant potentials of extracts of Annona muricata (Soursop). Food Sci Nutr 2017;5:1029–36.10.1002/fsn3.498Search in Google Scholar PubMed PubMed Central

[9] Mohamad Rosdi MN, Mohd Arif S, Abu Bakar MH, Razali SA, Mohamed Zulkifli R, Ya’akob H. Molecular docking studies of bioactive compounds from Annona muricata Linn as potential inhibitors for Bcl-2, Bcl-w and Mcl-1 antiapoptotic proteins. Apoptosis 2018;23:27–4010.1007/s10495-017-1434-7Search in Google Scholar PubMed

[10] Yap CV, Subramaniam KS, Khor SW, Chung I. Annonacin exerts antitumor activity through induction of apoptosis and extracellular signal-regulated kinase inhibition. Pharmacog Res 2017;9:378–83.10.4103/pr.pr_19_17Search in Google Scholar PubMed PubMed Central

[11] Nwokocha CR, Owu DU, Gordon A, Thaxter K, McCalla G, Ozolua RI, et al. Possible mechanisms of action of the hypotensive effect of Annona muricata (soursop) in normotensive Sprague-Dawley rats. Pharm Biol 2012;50:1436–41.10.3109/13880209.2012.684690Search in Google Scholar PubMed

[12] Hamid RA, Foong CP, Ahmad Z, Hussain MK. Antinociceptive and anti-ulcerogenic activities of the ethanolic extract of Annona muricata leaf. Rev Bras Farmacogn 2012;22:630–41.10.1590/S0102-695X2012005000001Search in Google Scholar

[13] De Sousa OV, Vieira GD, de Pinho JD, Yamamoto CH, Alves MS. Antinociceptive and anti-inflammatory activities of the ethanol extract of Annona muricata L. leaves in animal models. Int J Mol Sci 2010;11:2067–78.10.3390/ijms11052067Search in Google Scholar PubMed PubMed Central

[14] Qazi AK, Siddiqui JA, Jahan R, Chaudhary S, Walker LA, Sayed Z, et al. Emerging therapeutic potential of graviola and its constituents in cancers. Carcinogenesis 2018;39:522–33.10.1093/carcin/bgy024Search in Google Scholar PubMed PubMed Central

[15] Rady I, Bloch MB, Chamcheu RN, Banang Mbeumi S, Anwar MR, Mohamed H, et al. Anticancer properties of Graviola (Annona muricata): a comprehensive mechanistic review. Oxid Med Cell Longev 2018:1826170.10.1155/2018/1826170Search in Google Scholar PubMed PubMed Central

[16] Moreau D, Huchot E, Gazaille V, Rossanaly-Vasram R, Andre M. Self-medication with Annona muricata L. (corossol) as an anti-cancer agent in reunion. Rev Mal Respir 2018;35:948–55.10.1016/j.rmr.2018.08.001Search in Google Scholar PubMed

[17] Meer S, Akhtar N. Annona muricata extract containing pharmaceutical emulgels with and without penetration enhancer for depigmenting and antierythmic effects. Pak J Pharm Sci 2018;31:2683–8.Search in Google Scholar

[18] Souza DO, Dos Santos Sales V, de Souza Rodrigues CK, de Oliveira LR, Santiago Lemos IC, de Araújo Delmondes G, et al. Phytochemical analysis and central effects of Annona muricata Linnaeus: possible involvement of the gabaergic and monoaminergic systems. Iran J Pharm Res 2018;17:1306–17.Search in Google Scholar

[19] Choi M, Kang YR, Lim IS, Chang YH. Structural characterization of cellulose obtained from extraction wastes of Graviola (Annona muricata) leaf. Prev Nutr Food Sci 2018;23:166–70.10.3746/pnf.2018.23.2.166Search in Google Scholar PubMed PubMed Central

[20] Bento EB, Júnior FE, de Oliveira DR, Fernandes CN, de Araújo Delmondes G, Cesário FR, et al. Antiulcerogenic activity of the hydroalcoholic extract of leaves of Annona muricata Linnaeus in mice. Saudi J Biol Sci 2018;25:609–21.10.1016/j.sjbs.2016.01.024Search in Google Scholar PubMed PubMed Central

[21] Morosetti G, Criscuolo AA, Santi F, Perno CF, Piccione E, Ciotti M. Ellagic acid and Annona muricata in the chemoprevention of HPV-related pre-neoplastic lesions of the cervix. Oncol Lett 2017;13:1880–4.10.3892/ol.2017.5634Search in Google Scholar PubMed PubMed Central

[22] Antony P, Vijayan R. Acetogenins from Annona muricata as potential inhibitors of antiapoptotic proteins: a molecular modeling study. Drug Des Devel Ther 2016;10:1399–410.10.2147/DDDT.S103216Search in Google Scholar PubMed PubMed Central

[23] Magadi VP, Ravi V, Arpitha A, Litha, Kumaraswamy K, Manjunath K. Evaluation of cytotoxicity of aqueous extract of Graviola leaves on squamous cell carcinoma cell-25 cell lines by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and determination of percentage of cell inhibition at G2M phase of cell cycle by flow cytometry: an in vitro study. Contemp Clin Dent 2015;6:529–33.10.4103/0976-237X.169863Search in Google Scholar PubMed PubMed Central

[24] Soudani N, Sefi M, Ben Amara I, Boudawara T, Zeghal N. Protective effects of selenium (Se) on chromium (VI) induced nephrotoxicity in adult rats. Ecotoxicol Environ Saf 2010;73:671–8.10.1016/j.ecoenv.2009.10.002Search in Google Scholar PubMed

[25] Soudani N, Sefi M, Bouaziz H, Chtourou Y, Boudawara T, Zeghal N. Nephrotoxicity induced by chromium (VI) in adult rats and their progeny. Hum Exp Toxicol 2011;30:1233–45.10.1177/0960327110387454Search in Google Scholar PubMed

[26] Parveen K, Khan MR, Siddiqui WA. Pycnogenol prevents potassium dichromate K2Cr2O7-induced oxidative damage and nephrotoxicity in rats. Chem Biol Interact 2009;181:343–50.10.1016/j.cbi.2009.08.001Search in Google Scholar PubMed

[27] Barrera-Oviedo D, Carranza-Pérez MG, Candelario-Mota MT, Mendoza-Patiño N, Maldonado PD, Pedraza-Chaverrí J. Protective effect of SnCl2 on K2Cr2O7-induced toxicity in LLC-PK1 cells. Ren Fail 2013;35:132–27.10.3109/0886022X.2012.736071Search in Google Scholar PubMed

[28] Molina-Jijón E, Zarco-Márquez G, Medina-Campos ON, Zataraín-Barrón ZL, Hernández-Pando R, Pinzón E, et al. Deferoxamine pretreatment prevents Cr(VI)-induced nephrotoxicity and oxidant stress: role of Cr(VI) chelation. Toxicol 2012;291:93–101.10.1016/j.tox.2011.11.003Search in Google Scholar PubMed

[29] Khan MR, Siddiqui S, Parveen K, Javed S, Diwakar S, Siddiqui WA. Nephroprotective action of tocotrienol-rich fraction (TRF) from palm oil against potassium dichromate (K2Cr2O7)-induced acute renal injury in rats. Chem Biol Interact 2010;186:228–38.10.1016/j.cbi.2010.04.025Search in Google Scholar PubMed

[30] Wu Y, Connors D, Barber L, Jayachandra S, Hanumegowda UM, Adams SP. Multiplexed assay panel of cytotoxicity in HK-2 cells for detection of renal proximal tubule injury potential of compounds. Toxicol In Vitro 2009;23:1170–8.10.1016/j.tiv.2009.06.003Search in Google Scholar PubMed

[31] Sahu BD, Koneru M, Bijargi SR, Kota A, Sistla R. Chromium-induced nephrotoxicity and ameliorative effect of carvedilol in rats: Involvement of oxidative stress, apoptosis and inflammation. Chem Biol Interact 2014;223:69–79.10.1016/j.cbi.2014.09.009Search in Google Scholar PubMed

[32] Hegazy R, Salama A, Mansour D, Hassan A. Renoprotective effect of lactoferrin against chromium-induced acute kidney injury in rats: involvement of IL-18 and IGF-1 inhibition. PLoS One 2016;11:e0151486.10.1371/journal.pone.0151486Search in Google Scholar PubMed PubMed Central

[33] Cengiz M, Alansal NO, Tuncdemir M, Tanriverdi G, Bayoglu B. Evaluation of effects of melatonin and caffeic acid phenethyl ester on acute potassium dichromate toxicity and genotoxicity in rats. Indian J Pharmacol 2016;48:407–11.10.4103/0253-7613.186213Search in Google Scholar PubMed PubMed Central

[34] Wan H, Zhu Y, Chen P, Wang Y, Hao P, Cheng Z, et al. Effect of various selenium doses on chromium (IV)-induced nephrotoxicity in a male chicken model. Chemosphere 2017;174:306–14.10.1016/j.chemosphere.2017.01.143Search in Google Scholar

[35] Oyagbemi AA, Omobowale TO, Saba AB, Olowu ER, Dada RO, Akinrinde AS. Gallic acid ameliorates cyclophosphamide-induced neurotoxicity in Wistar rats through free radical scavenging activity and improvement in antioxidant defense system. J Diet Suppl 2016;13:402–19.10.3109/19390211.2015.1103827Search in Google Scholar

[36] Evans WC. Trease and Evans’ pharmacognosy, 15th ed. W.B. Saunders, Elsevier (A Division of Reed Elsevier India Pvt. Limited), 2002:221–31.Search in Google Scholar

[37] Sofowora AC. Medicinal plants and traditional medicine in Africa. Ibadan: Spectrum Books, 1993:261–8.Search in Google Scholar

[38] Misra HP, Fridovic I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 1972;247:3170–5.10.1016/S0021-9258(19)45228-9Search in Google Scholar

[39] Oyagbemi AA, Omobowale TO, Akinrinde AS, Saba AB, Ogunpolu BS, Daramola O. Lack of reversal of oxidative damage in renal tissues of lead acetate-treated rats. Environ Toxicol 2015;30:1235–43.10.1002/tox.21994Search in Google Scholar

[40] Jollow DJ, Mitchell JR, Zampaglione N. Bromobenzene induced liver necrosis. Protective role of glutathione and evidence for 3,4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacol 1974;11:151–69.10.1159/000136485Search in Google Scholar

[41] Shinha KA. Colorimetric assay of catalase. Anal Biochem 1972;47:389–94.10.1016/0003-2697(72)90132-7Search in Google Scholar

[42] Beutler E, Duron O, Kelly BM. Improved method for the determination of blood glutathione. J Lab Clin Med 1975;61:882–8.Search in Google Scholar

[43] Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases. The first enzymatic step in mercapturic acid formation. J Bio Chem 1972;25:7130–9.10.1016/S0021-9258(19)42083-8Search in Google Scholar

[44] Gornal AG, Bardawill JC, David MM. Determination of serum proteins by means of biuret reaction. J Biol Chem 1949;177:751–66.10.1016/S0021-9258(18)57021-6Search in Google Scholar

[45] Kayali R, Cakatay U, Akcay T, Altug T. Effect of alpha-lipoic acid supplementation on markers of protein oxidation in post-mitotic tissues of ageing rat. Cell Biochem Funct 2006;24:79–85.10.1002/cbf.1190Search in Google Scholar

[46] Wolff SF. Ferrous ion oxidation in the presence of ferric ion indicator xylenol orange for measurement of hydrogen peroxides. Methods Enzymol 1994;233:182–9.10.1016/S0076-6879(94)33021-2Search in Google Scholar

[47] Varshney R, Kale RK. Effect of calmodulin antagonists on radiation induced lipid peroxidation in microsomes. Int J Radiat Biol 1990;58:733–43.10.1080/09553009014552121Search in Google Scholar PubMed

[48] Reznick AZ, Packer L. Oxidative damage to proteins: spectrophotometric method for carbonyl assay. Methods Enzymol 1994;233:357–63.10.1016/S0076-6879(94)33041-7Search in Google Scholar

[49] Jacques-Silva MC, Nogueira CW, Broch LC, Flores EM, Rocha JB. Diphenyl diselenide and ascorbic acid changes deposition of selenium and ascorbic acid in liver and brain of mice. Pharm Toxicol 2001;88:119–25.10.1034/j.1600-0773.2001.d01-92.xSearch in Google Scholar PubMed

[50] Olaleye SB, Adaramoye OA, Erigbali PP, Adeniyi OS. Lead exposure increases oxidative stress in the gastric mucosa of HCl/ethanol-exposed rats. World J Gastroenterol 2007;13:5121–6.10.3748/wjg.v13.i38.5121Search in Google Scholar PubMed PubMed Central

[51] Xia Y, Zweier JL. Measurement of myeloperoxidase in leukocyte-containing tissues. Anal Biochem 1997;245:93–6.10.1006/abio.1996.9940Search in Google Scholar PubMed

[52] Akaike T, Ando M, Oda T, Doi T, Ijiri S, Araki S. Dependence on O2-generation by xanthine oxidase of pathogenesis of influenza virus infection in mice. J Clin Invest 1990;85:739–45.10.1172/JCI114499Search in Google Scholar PubMed PubMed Central

[53] Drury RA, Wallington EA, editors. Carlton’s histopathological techniques, 4th ed. London: Oxford University Press, 1976;139–42.Search in Google Scholar

[54] Oyagbemi AA, Omobowale TO, Ola-Davies OE, Adejumobi OA, Asenuga ER, Adeniji FK, et al. Protective effect of Azadirachta indica and vitamin E against arsenic acid-induced genotoxicity and apoptosis in rats. J Diet Suppl 2018;15:251–68.10.1080/19390211.2017.1336147Search in Google Scholar PubMed

[55] Oyagbemi AA, Omobowale TO, Asenuga ER, Adejumobi AO, Ajibade TO, Ige TM, et al. Sodium fluoride induces hypertension and cardiac complications through generation of reactive oxygen species and activation of nuclear factor kappa beta. Environ Toxicol 2017;32:1089–101.10.1002/tox.22306Search in Google Scholar PubMed

[56] Klinger JR, Kadowitz PJ. The nitric oxide pathway in pulmonary vascular disease. Am J Cardiol 2017;120:S71–9.10.1016/j.amjcard.2017.06.012Search in Google Scholar PubMed

[57] Pinheiro LC, Tanus-Santos JE, Castro MM. The potential of stimulating nitric oxide formation in the treatment of hypertension. Expert Opin Ther Targets 2017;21:543–56.10.1080/14728222.2017.1310840Search in Google Scholar PubMed

[58] Santos-Parker JR, Strahler TR, Bassett CJ, Bispham NZ, Chonchol MB, Seals DR. Curcumin supplementation improves vascular endothelial function in healthy middle-aged and older adults by increasing nitric oxide bioavailability and reducing oxidative stress. Aging (Albany NY) 2017;9:187–208.10.18632/aging.101149Search in Google Scholar PubMed PubMed Central

[59] Volpe CM, Villar-Delfino PH, Dos Anjos PM, Nogueira-Machado JA. Cellular death, reactive oxygen species (ROS) and diabetic complications. Cell Death Dis 2018;9:119.10.1038/s41419-017-0135-zSearch in Google Scholar PubMed PubMed Central

[60] Bartesaghi S, Radi R. Fundamentals on the biochemistry of peroxynitrite and protein tyrosine nitration. Redox Biol 2018;14:618–25.10.1016/j.redox.2017.09.009Search in Google Scholar PubMed PubMed Central

[61] Olaiya CO, Esan AM, Alabi TD. Ameliorative effects of β-sitosterol on some biochemical indices of hypertension in Wistar albino rats. Afr J Med Med Sci 2014;43:157–66.Search in Google Scholar

[62] Pracheta P, Veena S, Lokendra S, Ritu P, Sadhana S, Sachdev Y, et al. Chemopreventive effect of hydroethanolic extract of Euphorbia neriifolia leaves against DENA-induced renal carcinogenesis in mice. Asian Pacific J Cancer Prev 2011;12:677–83.Search in Google Scholar

[63] Ebner A, Kuerbis N, Brandt A, Zatschler B, Weinert S, Poitz DM, et al. Endothelial nitric oxide synthase-induced hypertrophy and vascular dysfunction contribute to the left ventricular dysfunction in caveolin-1-/-mice. Can J Cardiol 2017;33:1716–24.10.1016/j.cjca.2017.09.015Search in Google Scholar PubMed

[64] Jiang Y, Du W, Chu Q, Qin Y, Tuguzbaeva G, Wang H, et al. Downregulation of long non-coding RNA Kcnq1ot1: an important mechanism of arsenic trioxide-induced long QT syndrome. Cell Physiol Biochem 2018;45:192–202.10.1159/000486357Search in Google Scholar PubMed

[65] Tisdale JE. Drug-induced QT interval prolongation and torsades de pointes: role of the pharmacist in risk assessment, prevention and management. Can Pharm J (Ott) 2016;149:139–52.10.1177/1715163516641136Search in Google Scholar PubMed PubMed Central

[66] Lee DG, Lee J, Kim KT, Lee SW, Kim YO, Cho IH, et al. High-performance liquid chromatography analysis of phytosterols in Panax ginseng root grown under different conditions. J Ginseng Res 2018;42:16–20.10.1016/j.jgr.2016.10.004Search in Google Scholar PubMed PubMed Central

[67] Moustafa EM, Thabet NM. Beta-sitosterol upregulated paraoxonase-1 via peroxisome proliferator-activated receptor-γ in irradiated rats. Can J Physiol Pharmacol 2017;95:661–6.10.1139/cjpp-2016-0397Search in Google Scholar PubMed

[68] Yu LY, Shi WL, Guo XG. Cardio-protective role of gingerol along with prominent anti-diabetic cardiomyopathy action in a streptozotocin-induced diabetes mellitus rat model. Cell J 2017;19:469–75.Search in Google Scholar

[69] Abolaji AO, Ojo M, Afolabi TT, Arowoogun MD, Nwawolor D, Farombi EO. Protective properties of 6-gingerol-rich fraction from Zingiber officinale (Ginger) on chlorpyrifos-induced oxidative damage and inflammation in the brain, ovary and uterus of rats. Chem Biol Interact 2017;270:15–23.10.1016/j.cbi.2017.03.017Search in Google Scholar PubMed

[70] Malina DM, Fonseca FA, Barbosa SA, Kasmas SH, Machado VA, França CN, et al. Additive effects of plant sterols supplementation in addition to different lipid-lowering regimens. J Clin Lipidol 2015;9:542–52.10.1016/j.jacl.2015.04.003Search in Google Scholar PubMed

[71] Togar B, Türkez H, Stefano AD, Tatar A, Cetin D. Zingiberene attenuates hydrogen peroxide-induced toxicity in neuronal cells. Hum Exp Toxicol 2015;34:135–44.10.1177/0960327114538987Search in Google Scholar PubMed

[72] Paterson RR. Cordyceps – a traditional Chinese medicine and another fungal therapeutic biofactory. Phytochemistry 2008;69:1469–95.10.1016/j.phytochem.2008.01.027Search in Google Scholar PubMed PubMed Central

[73] Subal D, Nilesh B, Manjunath YS, Mallareddy P, Hariprasath K. Nephroprotective evaluation of ethanolic extract of the seeds of papaya and pumpkin fruit in cisplatin-induced nephrotoxicity. J Pharmaceut Sci Tech 2010;2:241–6.Search in Google Scholar

[74] Bellomo G, Selvi A. Uric acid: the lower the better? Contrib Nephrol 2018;192:69–76.10.1159/000484280Search in Google Scholar PubMed

[75] Richette P, Latourte A, Bardin T. Cardiac and renal protective effects of urate-lowering therapy. Rheumatology (Oxford). 2018;57:147–50.10.1093/rheumatology/kex432Search in Google Scholar PubMed

[76] Kiryluk K, Bomback AS, Cheng YL, Xu K, Camara PG, Rabadan R, et al. Precision medicine for acute kidney injury (AKI): redefining AKI by agnostic kidney tissue interrogation and genetics. Semin Nephrol 2018;38:40–51.10.1016/j.semnephrol.2017.09.006Search in Google Scholar PubMed PubMed Central

[77] Popov SV, Guseinov RG, Martov AG, Muratov TM, Tabynbaev NB. Biomarkers of acute hypoxia-reoxygenation injury to nercycites during laparoscopic resection of renal parenchyma. Urologiia 2017;6:120–5.Search in Google Scholar

[78] Li H, Liu Y, Gu Z, Li L, Liu Y, Wang L, et al. p38 MAPK-MK2 pathway regulates the heat-stress-induced accumulation of reactive oxygen species that mediates apoptotic cell death in glial cells. Oncol Lett 2018;15:775–82.10.3892/ol.2017.7360Search in Google Scholar PubMed PubMed Central

[79] Liu L, Zhong L, Zhao Y, Sexter A, Vaswani A, Smith SW, et al. Effect of lapatinib on cell proliferation and apoptosis in NB4 cells. Oncol Lett 2018;15:235–42.10.3892/ol.2017.7342Search in Google Scholar PubMed PubMed Central

[80] Shah AS, Sandoval Y, Noaman A, Adamson PD, D’Souza MS, Gray AJ, et al. Patient selection for high sensitivity cardiac troponin testing and diagnosis of myocardial infarction: prospective cohort study. Br Med J 2017;359:4788.10.1136/bmj.j4788Search in Google Scholar PubMed PubMed Central

[81] Bendary A, Tawfik W, Mahrous M, Salem M. Fibrinolytic therapy in patients with ST-segment elevation myocardial infarction: Accelerated versus standard streptokinase infusion regimen. J Cardiovasc Thorac Res 2017;9:209–14.10.15171/jcvtr.2017.36Search in Google Scholar PubMed PubMed Central

[82] de Filippi C, Seliger S. The cardiac troponin renal disease diagnostic conundrum: past, present, and future. Circulation 2018;137:452–4.10.1161/CIRCULATIONAHA.117.031717Search in Google Scholar PubMed

Received: 2018-06-23
Accepted: 2019-02-06
Published Online: 2019-05-03

© 2019 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Minireview
  2. Glial pathology in neuropsychiatric disorders: a brief review
  3. Original Articles
  4. Fenugreek seed extract ameliorates cognitive deficits in streptozotocin-induced diabetic rats
  5. The effect of silymarin supplementation on cognitive impairment induced by diabetes in rats
  6. Evaluation of the antianxiety and antidepressant activities of mosapride in Wistar albino rats
  7. Sexual stimulant effects of the mixture of Mondia whitei, Dracaena arborea, and Bridelia ferruginea in normal and prediabetic male Wistar rats
  8. Evaluating exercise challenge to validate cardiac autonomic dysfunction in lean PCOS phenotype
  9. Involvement of proinflammatory cytokines and metallothionein in the repairing of arsenic-mediated uterine tissue damage by curcumin
  10. Antioxidant potentials and effects on the hematology and osmotic fragility scores of a polyherbal formulation used in Southeast Nigeria
  11. Protective mechanisms of protocatechuic acid against doxorubicin-induced nephrotoxicity in rat model
  12. Phytochemicals and antidiabetic activity of the aqueous extract of the Punica granatum fruit in streptozotocin-induced diabetic mice
  13. Ficus cunia Buch.-Ham. ex Roxb. (leaves): An experimental evaluation of the cytotoxicity, thrombolytic, analgesic and neuropharmacological activities of its methanol extract
  14. Ameliorative effects of Annona muricata Linn. (Annonaceae) against potassium dichromate-induced hypertension in vivo: involvement of Kim-1/p38 MAPK/Nrf2 signaling
  15. Case Report
  16. A rare case of clomiphene-induced leukocytoclastic vasculitis
Downloaded on 11.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/jbcpp-2018-0172/html
Scroll to top button