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.2024 Oct 9;12(10):2285.
doi: 10.3390/biomedicines12102285.

The Effect of Nerolidol on Renal Dysfunction following Bilateral Ureteral Obstruction

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The Effect of Nerolidol on Renal Dysfunction following Bilateral Ureteral Obstruction

Harun R Toumi et al. Biomedicines..

Abstract

Background/Objectives: Obstructive uropathy is a common cause of renal impairment. Recently, there has been a burgeoning interest in exploring natural products as potential alternative remedies for many conditions due to their low toxicity, affordability and wide availability.Methods: We investigated the effect of nerolidol in a rat model of bilateral ureteral obstruction (BUO) injury. Nerolidol, dissolved in a vehicle, was administered orally as a single daily dose of 200 mg/kg to Wistar rats. Sham group (n = 12) underwent sham surgery, whereas the BUO (n = 12) and BUO/NR groups (n = 12) underwent reversible 24-h BUO and received the vehicle or nerolidol, respectively. The treatment started 9 days prior to the BUO/sham surgery and continued for 3 days after reversal. Renal functions were assessed before starting the treatment, just prior to the intervention and 3 days after BUO reversal.Results: Neither nerolidol nor the vehicle affected the basal renal functions. Nerolidol resulted in a significant attenuation in the BUO-induced alterations in renal functional parameters such as serum creatinine and urea, creatinine clearance and urinary albumin-creatinine ratio. Nerolidol also attenuated the changes in several markers associated with renal injury, inflammation, apoptosis and oxidative stress and mitigated the histological alterations.Conclusions: The findings of this study demonstrated the potent reno-protective effects of nerolidol in mitigating the adverse renal effects of bilateral ureteral obstruction. This is attributed to its anti-inflammatory, anti-fibrotic, anti-apoptotic and anti-oxidant properties. These effects were reflected in the partial recovery of renal functions and histological features. These findings may have potential therapeutic implications.

Keywords: acute kidney injury; bilateral ureteral obstruction; nerolidol.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Schematic presentation of the study plan showing interventions in all groups.
Figure 2
Figure 2
The gene expression of two of markers of acute renal injury (KIM-1 and NGAL) in all the groups. The values represent mean ± SEM.
Figure 3
Figure 3
The gene expression of pro-inflammatory markers: tumor necrosis factor-α (TNF-α), plasminogen activator inhibitor-1 (PAI-1), interleukin 1 beta (IL-1β), and interleukin-6 (IL-6) in all groups. The values represent mean ± SEM.
Figure 4
Figure 4
The gene expression of the oxidative stress markers: glutathione peroxidase (GPX-1) and glutathione-disulfide reductase (GSR) pro-apoptoticp53 gene in all groups. Values represent mean ± SEM.
Figure 5
Figure 5
The histological features in all the experimental groups. (A,B): G-sham control showing normal kidney architecture and histology. (C,D): G-BUO showing large areas of tubular injury with tubular dilatation (thin arrows) and intratubular secretions (arrowheads) in 44.2 ± 2.9% of the examined tissue areas. (E,F): G-BUO/NR-treated group showing foci of tubular injury with tubular dilatation (thin arrows) involving 27.8 ± 1.5% of examined tissue areas.
Figure 6
Figure 6
Summary of the effects of nerolidol on bilateral ureteral obstruction.
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References

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