Literature DB >> 30671613

β-Lapachone protects against doxorubicin-induced nephrotoxicity via NAD+/AMPK/NF-kB in mice.

Davoud Sanajou1, Saeed Nazari Soltan Ahmad1, Vahid Hosseini1,2, Ashkan Kalantary-Charvadeh1, Yasser Marandi3, Leila Roshangar2, Saman Bahrambeigi4, Mehran Mesgari-Abbasi5.   

Abstract

β-Lapachone (B-LAP) is a natural naphtaquinone with established anti-oxidative stress and anti-cancer activities. We aimed to investigate B-LAP protective potential against doxorubicin (DOX)-induced nephrotoxicity in mice. The mice received an oral dose of B-LAP followed by a single intraperitoneal injection of 20 mg/kg DOX a day later. They were then treated for 4 days with 1.25 mg/kg, 2.5 mg/kg, and 5 mg/kg doses of B-LAP. Renal levels of NAD+/NADH ratios, p-AMPKα, p-NF-κB p65, inducible nitric oxide synthase (iNOS), tumor necrosis factor alpha (TNF-α), interleukin 6 (IL-6) along with renal expressions of TNF-α, IL-1β, and IL-6 were examined. Serum levels of kidney function markers as well as renal histopathology were also investigated. In addition to increasing the activities of p-AMPKα, B-LAP elevated NAD+/NADH ratios in the kidneys and decreased the renal levels of nuclear p-NF-κB and its correspondent downstream effectors TNF-α, IL-1β, IL-6, and iNOS in the kidneys. Also, B-LAP effectively ameliorated renal architectural changes and attenuated serum levels of urea, creatinine, and cystatin C. Collectively, these findings suggest the protective actions of B-LAP against DOX-induced nephrotoxicity in mice.

Entities:  

Keywords:  Doxorubicin; NAD+/NADH ratio; Nephrotoxicity; β-Lapachone

Mesh:

Substances:

Year:  2019        PMID: 30671613     DOI: 10.1007/s00210-019-01619-0

Source DB:  PubMed          Journal:  Naunyn Schmiedebergs Arch Pharmacol        ISSN: 0028-1298            Impact factor:   3.195


  26 in total

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4.  Inhibition of AMPK signalling by doxorubicin: at the crossroads of the cardiac responses to energetic, oxidative, and genotoxic stress.

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Review 5.  Antagonistic crosstalk between NF-κB and SIRT1 in the regulation of inflammation and metabolic disorders.

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6.  Topoisomerase II alpha status in renal medullary carcinoma: immuno-expression and gene copy alterations of a potential target of therapy.

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Journal:  Exp Cell Res       Date:  2017-10-03       Impact factor: 3.905

8.  Selective killing of cancer cells by beta -lapachone: direct checkpoint activation as a strategy against cancer.

Authors:  Youzhi Li; Xiangao Sun; J Thomas LaMont; Arthur B Pardee; Chiang J Li
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-21       Impact factor: 12.779

9.  beta-Lapachone-induced apoptosis is associated with activation of caspase-3 and inactivation of NF-kappaB in human colon cancer HCT-116 cells.

Authors:  Byung Tae Choi; JaeHun Cheong; Yung Hyun Choi
Journal:  Anticancer Drugs       Date:  2003-11       Impact factor: 2.389

Review 10.  Pathophysiology and preventive strategies of anthracycline-induced cardiotoxicity.

Authors:  Woo-Baek Chung; Ho-Joong Youn
Journal:  Korean J Intern Med       Date:  2016-07-01       Impact factor: 2.884

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  1 in total

1.  β-LAPachone is renoprotective in streptozotocin-induced diabetic mice via regulating the PI3K/Akt/mTOR signaling pathway.

Authors:  Davoud Sanajou; Saman Bahrambeigi; Somayeh Aslani
Journal:  Iran J Basic Med Sci       Date:  2021-05       Impact factor: 2.699

  1 in total

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