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Involvement of Nrf2, JAK and COX pathways in acetaminophen-induced nephropathy: Role of some antioxidants
被引:4
作者:

Alqahtani, Qamraa H.
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King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia
King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh 11495, Saudi Arabia King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia

Fadda, Laila M.
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King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia

Alhusaini, Ahlam M.
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King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia

Hasan, Iman H.
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King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia

Ali, Hanaa M.
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Natl Res Ctr, Dept Genet & Cytol, Dokki, Egypt King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia
机构:
[1] King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia
[2] Natl Res Ctr, Dept Genet & Cytol, Dokki, Egypt
[3] King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh 11495, Saudi Arabia
关键词:
Acetaminophen;
Thymoquinone;
Curcumin;
N-acetylcysteine;
& alpha;
-Lipoic acid;
Nrf2;
JAK;
COX;
ALPHA-LIPOIC ACID;
INDUCED NEPHROTOXICITY;
CURCUMIN PROTECTS;
OXIDATIVE STRESS;
THYMOQUINONE;
FAILURE;
JAK/STAT;
KIDNEY;
MAPK;
CARE;
D O I:
10.1016/j.jsps.2023.101752
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Objectives: Acetaminophen (APAP)-induced nephrotoxicity is detrimental consequence for which there has not been a standardized therapeutic regimen. Although, N-acetylcysteine (NAC) is a well-known antidote used in APAP-induced hepatotoxicity, its benefit in nephrotoxicity caused by APAP is almost lacking. This study aimed to compare the possible protective effect of thymoquinone (TQ), curcumin (CR), and a- lipoic acid (a-LA), either in solo or in combination regimens with that of NAC against APAP-induced renal injury.Design and method: Rats were divided into nine groups; control group, APAP intoxicated group (1000 mg/kg; orally), and the remaining seven groups received, in addition to APAP, oral doses of NAC, TQ, CR, a-LA, CR plus TQ, TQ plus a-LA, or CR plus a-LA. The first dose of the aforementioned antioxidants was given 24 h before APAP, and then the second dose was given 2 h after APAP, whereas the last dose was given 10 h after administration of APAP.Results: Treatment with APAP elevated kidney markers like serum uric acid, urea, and creatinine. In addition, it increased the serum level of tumor necrosis factor alpha (TNF-a), interleukin-1beta (IL-1b) and thiobarbituric acid reactive species (TBARS). Also, the protein expression of renal janus kinase (JAK) and cyclooxygenase (COX)-2 were all upregulated by APAP. In contrast, the expression of Nrf2 and the renal levels of superoxide dismutase and glutathione were downregulated. Treatment with the indicated natural antioxidants resulted in amelioration of the aberrated parameters through exhibiting antiinflammatory, antioxidant and free radical-scavenging effects with a variable degree.Conclusion: The combined administration of CR and TQ exerted the most potent protection against APAPinduced nephrotoxicity through its anti-inflammatory and free radical-scavenging effects (antioxidant) which were comparable to that of NAC-treatment.
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Yonsei Univ, Coll Human Ecol, Dept Food & Nutr, Brain Korea PLUS Project 21, Seoul 03722, South Korea Yonsei Univ, Coll Human Ecol, Dept Food & Nutr, Brain Korea PLUS Project 21, Seoul 03722, South Korea

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Yonsei Univ, Coll Med, Dept Pharmacol, Seoul 03722, South Korea Yonsei Univ, Coll Human Ecol, Dept Food & Nutr, Brain Korea PLUS Project 21, Seoul 03722, South Korea

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Abdeen, Ahmed
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Benha Univ, Fac Vet Med, Dept Forens Med & Toxicol, Toukh 13736, Qaliobiya, Egypt Benha Univ, Fac Vet Med, Dept Pharmacol, Toukh 13736, Qaliobiya, Egypt

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Benha Univ, Fac Vet Med, Dept Pharmacol, Toukh 13736, Qaliobiya, Egypt Benha Univ, Fac Vet Med, Dept Pharmacol, Toukh 13736, Qaliobiya, Egypt