The role of protein prenylation inhibition through targeting FPPS by zoledronic acid in the prevention of renal fibrosis in rats

Renal fibrosis (RF) represents the most widespread pathological condition in chronic kidney disease (CKD). Recently, protein prenylation has been implicated in the fibrosis’s progression. The research examined the renoprotective effect of zoledronic acid (ZA) (50 µg/kg/week) in a rat model of carbon tetrachloride (CCl4)-induced RF through targeting protein prenylation. Forty Wistar male rats were split up into the control group, vehicle-treated group, model-RF group, and RF-ZA group. Mean arterial blood pressure (MBP), BUN, serum creatinine, and urine albumin–creatinine ratio (uACR), protein levels of farnesyl pyrophosphate (FPP), tumour necrosis factor-alpha (TNF-α), transforming growth factor-β (TGF-β), and malondialdehyde (MDA), and catalase and gene expression of farnesyl pyrophosphate synthase (FPPS) and nuclear factor-kB (NF-κB) were measured. Immunohistochemical staining for renal interleukin-6 (IL-6), α-smooth muscle actin (α-SMA), and caspase-3, as well as histopathological alterations, were assessed. ZA considerably ceased the reduction in MBP, markedly reduced uACR, serum creatinine, BUN, and expression of FPPS, FPP, NF-κB, TGF-β, TNF-α, and MDA, and significantly increased catalase levels compared to the model-RF rats. ZA ameliorated the CCl4-induced histopathological alterations and suppressed the expression of caspase-3, α-SMA, and IL-6. In conclusion, ZA preserved renal function and prevented renal fibrosis in a rat model. These were achieved through targeting protein prenylation mainly by inhibiting FPPS.


Ethical approval
All animal procedures were carried out in accordance with ARRIVE guidelines 17 .The study was approved by the Ain Shams University, Faculty of Medicine's Institutional Animal Ethics Committee.The application approval number was FMASU MD R115/2023, which runs according to the guidelines of the International Council on Harmonization (ICH) for Medical Science (IOMS), the United States Office for Human Research.The animal experiment was done according to the guidelines of ethical care and standard regulations.
Zoledronic acid (ZA) was supplied by Sigma Aldrich Chemicals, as a white powder as a white powder dissolved in 0.9% saline.ZA was created by combining 0.05 mL of the chemical with 0.95 mL of normal saline, resulting in a concentration of 0.05 mg/ml ZA.A transparent mixture of carbon tetrachloride (CCl 4 ) and sterilized olive oil was provided in a 1:1 ratio, at a dosage of 4 mL per kilogram of total volume.
The dose of ZA to osteoporotic patients is ranging from 4 to 5 mg 18 .We extrapolated the clinical dose of the drug received by patients for osteoporosis treatment (4 mg) according to rats' weight, metabolic rates, and treatment period protocols.For the Wistar rats, the calculated dosage was 0.60 mg/kg.Then, it was split to be administered for 12 weeks to 50 µg/kg/week 19,20 .

Measurement of mean blood pressure (MBP)
At the end of the experiment and before rats' scarification, (45 mg/kg, i.p.) sodium pentobarbital was used for the anesthesia of rats, followed by insertion of the tube intratracheally and opening of the wall of the anterior abdomen.By cannulating the abdominal aorta with a polyethylene catheter (PE50) loaded with heparinized saline (100 U/ml) and attached to a physiological pressure transducer (SP844) manufactured by Power Lab (AD Instruments, Germany), the mean blood pressure (MBP) was measured.

Measurement of urine albumin-creatinine ratio (uACR)
The collection of 24 h rats' urine was done in metabolic cages before scarification.The concentration of urinary microalbumin (mg/24 h) was measured using a rat albumin ELISA kit (Gen Way Biotech, San Diego).The concentration of urinary creatinine (g/24 h) was measured using QuantiChrom Creatinine ELISA kit (BioAssay Systems, USA) and Creatinine Jaffè ELISA kit (Spectrum, Egyptian Company for Biotechnology).The procedures were performed in compliance with the manufacturer's guidelines.

Measurement of serum creatinine and blood urea nitrogen (BUN) levels
Using aseptic techniques, blood was drawn from all experimentally sedated animals through retroorbital perforation.The specimens were centrifuged at 1000g for 15 min after being left to coagulate for 2 h at room temperature.After extraction, the serum specimens were kept at − 80 °C.The concentration of creatinine in serum (nmol/ml) was calculated with a creatinine (Rat) ELISA kit (BioVision, USA, Cat.No. E4370-100).The concentration of urea in serum (nmol/ml) was measured using rat blood urea nitrogen (BUN) ELISA kit (SunLong Biotech Co., Cat.No. SL1053Ra).The procedures were performed per the guidelines provided by the manufacturer.

Molecular studies
Left kidneys were removed after scarification, and renal tissue homogenization was done using phosphate buffer saline (10% PBS).To 4 g of tissue, 16 mL of 10% PBS were added and spent 20 min centrifuging at 2000g, www.nature.com/scientificreports/followed by freezing of the supernatant at − 80 °C till examination.Assessment of the specimens was done for the subsequent criteria.

Measurement of tumor necrosis factor-alpha (TNF-α) and transforming growth factor-β (TGF-β) in kidney tissue
The tissue level of TNF-α was assessed by the ELISA MAX ™ Deluxe Set (Biolegend et al., Cat.No. 438206).In contrast, tissue TGF-β was quantified using an ELISA kit (Cloud-Clone Corp., USA, Cat.No. SEA124Ra) in compliance with the manufacturer's guidelines.

Measurement of farnesyl pyrophosphate (FPP) in kidney tissue
The concentration of FPP was estimated in kidney tissue with the use of rat squalene synthase, FDFT1 ELISA kit (Cat.No: MBS9331891).

Gene expression analysis for farnesyl pyrophosphate synthase (FPPS) and nuclear factor-κB (NF-κB) by real-time quantitative polymerase chain reaction (RT-qPCR)
RNA extraction.The whole RNA has been extracted from homogenized tissues of each group using Direct-zol RNA Miniprep Plus (Cat.No: R2072, ZYMO RESEARCH CORP., the United States), and then both quality and quantity were assessed using a Beckman dual spectrophotometer (USA).
Real-time PCR.Using a SuperScript IV One-Step RT-PCR kit (Cat# 12594100, Thermo Fisher Scientific, Waltham, MA, USA), extracted RNA was reverse transcribed to cDNA and then subjected to PCR.Primer's sequence used for amplification of NFκB gene was forward 5′-GTC TCA AAC CAA ACA GCC TCAC -3′, and reverse 5′-CAG TGT CTT CCT CGA CAT GGAT -3′ (gene bank accession number NM_199267.2).FPPs gene was forward 5′-TGG TGT GTA GAA CTG CTC CAG GCT TTC TTC -3′, and reverse 5′-ACA CTG GGG TCT CCA AAG AGA TCA AGG TAG -3′ (gene bank accession number NM_031840), and GAPDH housekeeping gene was forward 5′-CCT CGT CTC ATA GAC AAG ATGGT -3′ and reverse 5′-GGG TAG AGT CAT ACT GGA ACATG -3′ (gene bank accession number NM_001394060.2).On a plate with 96 wells, the StepOne instrument (Applied Biosystems, USA) was used in the following way for a thermal profile: reverse transcription is carried out for 10 min at 45 ºC, RT inactivation for 2 min at 98 ºC, and initial denaturation is carried out in 40 cycles of 10 s at 98 ºC, 10 s at 55 ºC, and 30 s at 72 ºC for the amplification step.The data for the target genes and housekeeping genes was provided in cycle threshold (Ct) following the RT-PCR run.Normalization of target gene expression variation; NFκB and FPPS were carried out relating for the expression for the mean critical threshold (CT) values of the GAPDH housekeeping gene by the ΔΔCt method.The 2 −∆∆Ct method is utilized to calculate the relative quantitation (RQ) of every target gene 23 .Figures S1 and S2.

Histopathological and immunohistochemical study
The right kidney was taken from all animals through an abdominal incision.Kidneys were divided longitudinally into two halves.Then, they were fixed in 10% formalin over 5 days.Following a dehydration process using increasing alcohol grades, the samples were cleaned in xylene and placed in paraffin.Sections of paraffin were cut in serial at 5 μm thickness 24 .Several procedures were applied to paraffin sections: Haematoxylin and eosin (H&E) and picro sirius red stain (ab150681; Abcam, MA, USA) for demonstration of collagen fibers.Additional sections were sliced and put on positively charged slides for immune-histochemical staining with an anticaspase-3 antibody using the avidin-biotin peroxidase method [Mouse monoclonal-ABM1C12] (ab208161; Abcam, MA, USA), Anti-IL-6 antibody [mouse monoclonal 1.2-2B11-2G10] (ab9324; Abcam, MA, USA) and anti-alpha smooth muscle actin (α SMA) antibody [mouse monoclonal [1A4] (ab7817; Abcam, MA, USA).We used hematoxylin to counterstain the slides.Similar procedure was followed when processing negative controls, but without using the primary antibody.Positive control sections for caspase-3, IL-6 and α-SMA were examined utilizing sections of the tonsil, kidney, and colon (respectively) and this was done according to the same protocol.
Caspase-3 reaction was done for demonstration of apoptosis.IL-6 was done for demonstration of inflammatory cells and α-SMA was done for demonstration of smooth muscle cells in vascular structures as well as myofibroblasts.The positive reaction appeared as brown cytoplasmic reaction.

Histo-morphometric studies and analytical statistics
A computer with the Leica Q win V.3 image analyzer program installed was used.The Leica DM2500 microscope (Wetzlar, Germany) was linked to the computer.Every group of animals underwent morphological analysis.Five distinct slides were obtained from each animal, and measurements were made from them.For every slide, five randomly chosen, not-overlapping fields were looked at.The following parameters were measured: 1-The diameter of the PCT in H & E-stained sections (X400).2-Area % of collagen fibers in picrosirius red sections with stains (X200).3-Area % of caspase-3 immune-histochemical reaction (X400).4-Area % of IL-6 immune-histochemical reaction (X400).Every study's morphometric data was gathered and then statistically examined.The SPSS statistical software, version 21, was used to determine the mean value and the standard deviation (SD) for each group (IBM Inc., Chicago, Illinois, USA).One-way analysis of variance (ANOVA) was used to statistically analyze the data, and a post-hoc test was used to compare the means.The data was displayed as mean ± SD.The probability of chance (P-value) was used to assess the significance of the data; a value of P < 0.001 was interpreted as highly significant, a value of P < 0.05 was interpreted as significant, and a value of P > 0.05 was interpreted as non-significant.

Statistical analysis
For each group, the results except for morphometric studies were expressed as mean ± SD.GraphPad Prism, software application version 5.0 (2007), Inc., CA, USA, was used for statistical analysis.When comparing more than two groups, Tukey's multiple comparison test was performed after the one-way ANOVA was used to determine the statistical difference between the groups.Statistical significance was defined as P values of 0.05.

Results
There were no significant differences seen between the vehicle-treated group and the control group across all evaluated parameters.Thus, for comparisons with the model-RF and RF-ZA groups, the control group was used.There was no mortality in all groups throughout the 12 week study.

Effects on kidney index
According to the data presented in Table 1, the kidney index in the model-RF group showed a substantial rise of 59.7% compared to the control group, with a statistically significant difference (P < 0.0001).It is noteworthy that the administration of ZA at a dosage of 50 µg/kg/week resulted in a substantial (P < 0.0001) reduction in the kidney index by 32.3%.

Effects on Mean blood pressure (MBP)
The model-RF group had a significant reduction (P < 0.0001) in MBP compared to the control group, with a decrease of 63.7%.The administration of ZA at a dosage of 50 µg/kg/week effectively (P < 0.0001) prevented a reduction in the mean arterial pressure (MBP) by 162.5% (Table 1).

Urinary albumin to creatinine ratio (uACR)
The level of uACR was found to be considerably higher (P < 0.0001) in the model-RF group compared to the control group, with an increase of 236.4%.The group treated with RF-ZA exhibited a statistically significant (P < 0.0001) decrease in uACR compared to the model-RF group, with a reduction of 62.2% (Table 1).

Serum creatinine and blood urea nitrogen (BUN) levels
The model-RF group exhibited a statistically significant (P < 0.0001) elevation in serum creatinine and BUN levels compared to the control group, with increases of 261.9% and 192.6% respectively.Conversely, the RF-ZA treated group demonstrated a statistically significant (P < 0.0001) reduction in serum creatinine and BUN levels compared to the model group, with decreases of 67.1% and 62.9% respectively (Table 1).

Effects on oxidative stress markers: malondialdehyde (MDA) and catalase levels
According to the data shown in Table 2, the model-RF group exhibited a statistically significant increase (P < 0.0001) in the concentration of MDA in comparison to the control group, with a rise of 354.5%.The group treated with RF-ZA had a statistically significant (P < 0.0001) decrease in MDA levels compared to the model-RF group, with a reduction of 72.7%.In contrast, there was a substantial drop (P < 0.0001) in the catalase level observed in the model-RF group compared to the control group, with a decrease of 68.9%.Additionally, the administration of ZA to rats resulted in a large rise (P < 0.0001) in the renal content of catalase compared to the model-RF group, with an increase of 190.5%.

Effects on tumor necrosis factor-α (TNF-α) and transforming growth factor-β (TGF-β) levels
In the model-RF group, there was a substantial increase (P < 0.0001) in the levels of renal TNF-α and TGF-β compared to the control group, with an increase of 530.1% and 485.4% respectively.The administration of ZA to rats resulted in a significant reduction (P < 0.0001) in the renal levels of TNF-α and TGF-β, with a decrease of 74.0% and 81.7% respectively, as compared to the model-RF group (Table 2).

Effects on renal farnesyl pyrophosphate (FPP) protein level
According to the data shown in Table 2, there was a substantial increase (P < 0.0001) in the renal FPP level seen in the model-RF group compared to the control group, with an increase of 81.9%.The group treated with RF-ZA had a statistically significant (P < 0.0001) reduction in renal FPP level by 39.9% compared to the model-RF group.

Effects on renal farnesyl pyrophosphate synthetase (FPPS) and nuclear factor-kappa B (NF-kB) gene expressions
It was found that renal FPPS and NF-kB expression were significantly (P < 0.0001) upregulated in the model-RF group compared to the control group by 460% and 690.9%, respectively.RF-ZA treated group showed a significant (P < 0.0001) down-regulation of renal FPPS and NF-kB expression in comparison to the model-RF group by 76.8% and 86.2% respectively (Table 2).

Histological and histomorphometric results
Examination of the control and vehicle groups showed similar findings and represented as "control group".Statistical results revealed non-significant differences between the control group and the vehicle group (control groups) in all measured parameters.
H & E-stained slides of the control group showed that the renal cortex was consisted of the renal corpuscles surrounded with closely packed renal tubules.The renal corpuscles were seen with tuft of capillaries surrounded by Bowman's capsule.Bowman's capsule was composed of visceral and parietal layers with Bowman's space inbetween.The parietal layer was consisted of simple squamous cells.The proximal convoluted tubules (PCTs) were composed of cuboidal cells with spherical basal nuclei and heavy acidophilic cytoplasm.While the distal convoluted tubules (DCTs) were formed of low cuboidal cells with pale eosinophilic cytoplasm and round central to apical nuclei.The DCTs had wider lumina than the PCTs (Fig. 2A).In Model group, the histopathological changes were observed in the cortex including the glomeruli and the tubules.Most renal corpuscles were seen with irregular outline.Some corpuscles were seen with disrupted parietal layer of Bowman's capsule.Most renal tubules were dilated with sloughing of their epithelial cells inside the lumina with intraluminal acidophilic material.Vacuolated renal tubular cells were also noticed.Some tubules also showed pyknotic nuclei.Mononuclear cell infiltration was frequently seen in the renal interstitium.Dilated and congested glomerular and peritubular capillaries were also noticed (Fig. 2B-D).In zoledronate group, some areas showed apparent typical renal corpuscles surrounded with closely packed renal tubules.Other areas showed shrunken glomeruli.Some vacuolated tubular cells were also noticed.Glomerular and peritubular vascular congestion was occasionally seen (Fig. 2E, F).
The mean tubular diameter of the PCTs showed a highly significant difference between the different groups (f = 22.931, P < 0.001) by using one-way ANOVA.Compared to the control group, Post Hoc LSD showed a highly significant increase in the mean tubular diameter in the model group (P < 0.001).Also, there was significant increase in the mean tubular diameter in the RF-ZA group (P = 0.048).Meanwhile, there was a highly significant decrease in the mean tubular diameter in the RF-ZA group compared to the model-RF group (P < 0.001) (Table 3 and Fig. 3).
Kidney sections were stained with picrosirius red stain for demonstration of collagen fibers.By examination of the control group slides, few collagen fibers were revealed around renal corpuscles, renal tubules and around blood vessels (Fig. 4A).While in the model-RF, increased collagen fibers were noticed around blood vessels, renal tubules, and renal corpuscles.The amount of the collagen fibers was also observed to be increased inside most renal glomeruli (Fig. 4B) with a highly significant increase in the mean area % of collagen fibers compared   www.nature.com/scientificreports/ to the control group (P < 0.001).In RF-ZA group, decreased collagen fibers were noticed with highly significant decrease in the mean area % of collagen fibers compared to model-RF group (P < 0.001) (Fig. 4C).A highly significant difference in the mean area % of collagen fibers was noticed between the different groups (f = 131.500,P < 0.001).Post Hoc LSD showed There was also a significant increase in the mean area % of collagen fibers in the RF-ZA group compared to the control group (P = 0.004) (Table 3 and Fig. 5).
Examination of immunohistochemical caspase-3 slides of control group revealed minimal positive reaction in the cytoplasm of some tubular cells and cells inside few renal corpuscles (Fig. 6A), whereas, in model-RF group, intense positive cytoplasmic immune reaction was seen in most renal tubules with a highly significant increase in the mean area % of caspase-3 compared to the control (P < 0.001) (Fig. 6B).While RF-ZA group showed mild positive cytoplasmic caspase-3 reaction in some renal tubules with highly significant decrease in the mean area % of caspase-3 compared to the Model-RF (P < 0.001) (Fig. 6C).A highly significant difference in the mean area % of caspase-3 was noticed between the different groups (f = 56.597,P < 0.001).Post Hoc LSD also showed a significant increase in the mean area % of caspase-3 in the RF-ZA group compared to the control group (P = 0.002).(Table 3 and Fig. 5).
Regarding IL-6 immunohistochemical reaction, minimal positive reaction was noticed in the control group which was confined mostly to the peritubular capillaries (Fig. 7A).While the model group sections revealed intense positive expression with a highly significant increase in the mean area % of IL-6 compared to the control   rats (P < 0.001).The reaction was noticed in the cytoplasm of cells inside the glomeruli and in the renal interstitium mostly in peritubular capillaries (Fig. 7B).In RF-ZA group, mild reaction was noticed in some cells inside renal glomeruli and surrounding renal tubules with a highly significant decrease in the mean area % of IL-6 compared to the model-RF group (P < 0.001) (Fig. 7C).A highly significant difference in the mean area % of IL-6 was noticed between the different groups (f = 66.877,P < 0.001).There was also significant increase in the mean area % of IL-6 in the RF-ZA group compared to the control group (P = 0.002) (Table 3 and Fig. 5).
In α-SMA immunohistochemical sections of the control group minimal positive reaction was detected in the walls of the blood vessels.While the glomeruli and the tubules revealed negative reaction (Fig. 8A).In model-RF group intense positive reaction was noticed with a high significant increase in the mean area % of α-SMA compared to the control group (P < 0.001).The reaction was seen inside most renal glomeruli, in the walls of blood vessels and in some renal tubular epithelial cells (Fig. 8B).In RF-ZA group, mild positive reaction was seen with high significant decrease in the mean area % of α-SMA compared to model-RF group (P < 0.001).The reaction was seen in the walls of the blood vessels and inside some renal glomeruli, while negative reaction was seen in renal tubules (Fig. 8C).A highly significant difference in the mean area % of α-SMA was noticed between the different groups (f = 74.471,P < 0.001).There was also high significant increase in the mean area % of α-SMA in RF-ZA group compared to the control group (P < 0.001) (Table 3 and Fig. 5).

Discussion
In this study, we induced renal fibrosis (RF) in rats by using carbon tetrachloride (CCl 4 ).Research showed that CCl 4 causes oxidative stress and triggers the production of cytokines such as tumor necrosis factor-alpha (TNFα) and growth factors like transforming growth factor-β (TGF-β) in renal tissues.CCl 4 enhances apoptosis by stimulating the caspase pathway, resulting in renal damage 21 .Additionally, CCl 4 boosts protein prenylation, such as protein farnesylation and geranylgeranylation, by upregulating the production of farnesyl pyrophosphate (FPP) and geranylgeranyl pyrophosphate (GGPP) through the stimulation of reactive oxygen species (ROS) 7,25 .
The study indicated that zoledronic acid (ZA) at 50 µg/kg/week has a protective effect on the kidneys in a rat model of renal failure produced by CCl 4 .ZA markedly enhanced kidney functioning.It reduced elevated levels of urine albumin-creatinine ratio (uACR), serum creatinine, and blood urea nitrogen (BUN).The results included a notable reduction in the protein levels of tumor necrosis factor-alpha (TNF-α), transforming growth factor-β (TGF-β), and malondialdehyde (MDA), along with a considerable increase in catalase protein level in renal tissues.The beneficial benefits may be attributed to ZA's capacity to hinder the renal production of farnesyl pyrophosphate synthase (FPPS) and farnesyl pyrophosphate (FPP), leading to improved protein prenylation and decreased expression of nuclear factor-κB (NF-κB).
Protein prenylation is involved in cardiovascular, bone, and neurodegenerative illnesses.It is crucial in the advancement and growth of fibrosis by activating the NF κB signaling pathway.Hence, prenylation has emerged as an appealing target for inhibitors with potential therapeutic benefits 4,26 .
FPPS is a vital enzyme in the mevalonate pathway responsible for synthesizing isoprenoid intermediates like FPP 27 .FPP is necessary for the prenylation of RhoGTPases that trigger the NF κB signaling pathway, which www.nature.com/scientificreports/ is activated in fibrotic diseases 4 .Previous studies have confirmed that increased FPPS expression leads to the development of liver and lung fibrosis as well as heart hypertrophy [28][29][30][31] .Renal fibrosis, a critical pathological alteration in the progression of chronic kidney disease to end-stage renal disease, is heavily influenced by the NF-κB signaling system.The primary function of NF-κB is to augment the secretion of TNF-κ, IL-6, and TGF-β, resulting in notable fibrotic buildup and infiltration of inflammatory cells into the renal tissue.It was reported that macrophages infilteration and polarization aggravate renal inflammation and fibrosis 32,33 .Suppressing macrophages polarization and fibroblasts activation attenuates extracellular matrix protein production, and preserves kidney function 34,35 .In rheumatoid factor, IL-6 plays a pivotal role.The expression of the IL-6 gene is regulated by the NF-κB pathway.Tumor necrosis factor-alpha (TNF-α), predominantly found in renal tubular cells, can trigger an inflammatory response and lead to renal fibrosis 12,22,36 .
Increasing amounts of reactive oxygen species (ROS) and isoprenoid substrates stimulate renal fibrosis via boosting TGF-β signaling via the NF-κB signaling pathway 37,38 .TGF-β stimulates the attraction, specialization, and persistence of myofibroblasts identified by the presence of α-smooth muscle actin (α-SMA) and increased matrix accumulation, resulting in renal fibrosis.Activating transforming growth factor-beta (TGF-β) is essential for inducing epithelial-to-mesenchymal transition (EMT) in renal tubular cells, hence leading to the progression of renal interstitial fibrosis 39,40 .Therefore, targeting of NF-κB through inhibition of protein prenylation by the inhibition of FPPS has entered the spotlight.
It was reported that ZA, by inhibiting FPPS, reduced NF-κB signaling, decreased inflammatory cell recruitment, inhibited myofibroblast transition, reduced migration of pro-fibrotic cell populations, and eventually ameliorated lung fibrosis 13 , hepatic fibrosis 14 and myocardial fibrosis 41 .Göbel et al. 42 , did a study that provides evidence for the efficacy of ZA treatment in suppressing the activity of TGF-β, TNF-α, and IL-6 in ovarian cancer cells through the inhibition of the FPPS.
The study found that continuous exposure to CCl 4 caused structural changes in kidney tissues and led to a notable rise in the average area of caspase-3 in renal tubules and α-smooth muscle actin (α-SMA) in the peritubular capillaries and renal glomeruli.Additionally, there was a notable rise in the average area % of collagen fiber within renal glomeruli and in the renal interstitium.The results were consistent with prior experimental investigations that found CCl 4 treatment caused kidney damage, cell death, and increased production of the apoptosis-related protein caspase-3 22,43 .Previous investigations have shown that in certain kidney diseases, mesangial cells undergo a transformation into myofibroblasts.Alpha-smooth muscle actin (α-SMA) is a biomarker for myofibroblasts, which are cells that overproduce collagen 44,45 .
ZA at a modest dose of 50 µg/kg/week improved the histological changes in renal tissues caused by CCl 4 .ZA suppressed the expression of interleukin-6 (IL-6), α-SMA, and caspase-3 via reducing FPPS expression and decreasing FPP protein levels in renal tissues.The results of our study provide evidence for the efficacy of statins in inhibiting the production of isoprenoids, specifically FPP and GGPP, showing encouraging anti-fibrotic effects 46,47 .Statin disrupts isoprenoid synthesis, which inhibits NF-κB activation and TNF-α generation, leading to contrasting inflammatory and fibrosis effects 48 .Furthermore, this study found that model-RF rats exhibited a low mean blood pressure (MBP).ZA (50 µg/kg/ week) markedly enhanced MBP in ZA-RF rats compared to model-RF rats.The increase in MBP may be because to the improvement of renal functioning by ZA.The kidneys regulate blood pressure through mechanisms such as fluid balance, electrolyte management, and the renin-angiotensin-aldosterone system.End-stage renal disease can lead to reduced generation and effectiveness of angiotensin II, causing vasodilation and lowering blood pressure 49 .
Conflicting research results exist regarding the effect of ZA on renal function.Zoledronic acid (ZA) is the most effective bisphosphonate for treating bone problems related to cancer.ZA is commonly used when patients have impaired kidney function due to diseases including hypertension, diabetes, age-related renal insufficiency, or cancer -induce renal disease.Moreover, it is characterized by widespread approval, enabling safe and lasting integration 16,50 .Previous clinical trials found no link between yearly infusions of ZA and decline in kidney function in postmenopausal patients with osteoporosis 51,52 .Other studies suggest that ZA may lead to nephrotoxicity.In one of these trials, a higher dose of 3 mg/kg was provided compared to the level utilized in our investigation 53 .A different study found that ZA treatment resulted in decreased kidney function in rats with renal ischemia-reperfusion injury, but not in normal rats like in our investigation 15 .Bergner and his colleagues detected reduced renal function in rats with ZA in a dose of 1 mg/kg for a longer duration (27 weeks) than the duration of our study 54 .In patients treated with ZA at recommended doses and infusion rates, renal toxicity is rare, as confirmed by long-term data from clinical trials [55][56][57][58] .
The study used a dose of 50 µg/kg/week of ZA for 12 weeks to replicate the clinical dose given to human patients with osteoporosis.Additionally, it was shown that a ZA dose exceeding 200 µg/kg/week is deemed high for Wistar rats.The 4 mg ZA medication dosage given monthly to cancer patients is appropriate for preventing metastases [59][60][61] .The ZA dose (< 200 µg/kg/week) is considered minimal and is comparable to the doses administered intravenously for treating osteoporosis patients 62,63 .The nephrotoxicity of ZA depends on the dosage and duration of treatment.It is common in patients with severe renal impairment.Zoledronic acid is contraindicated only in cases of substantial renal insufficiency (stage IV-V, GFR 30 ml/min) 16 .The incidence of hypertension, diabetes, obesity, and other conditions leading to kidney damage and CKD is increasing annually, making CKD a major health concern 12 .Therefore, there is a requirement for pharmacological therapy that is both efficient and secure.ZA may be a viable treatment for preventing the progression of chronic kidney disease (CKD) and renal failure (RF) in high-risk patients.
Although our study has important implications, it also has limits that must be acknowledged.First, we focused on the effect of ZA on FPPS, FPP and NFκB parameters in protein prenylation pathway.However, they are not the only possible mediators of protein prenylation pathway.Therefore, the effect of ZA on other parameters that have an important role in protein prenylation induced fibrosis should be evaluated as RhoGTPases which are involved in activating NFκB signaling pathway.Determination of kidney injury score is one of important parameters that should be evaluated.Second, the effect of this dose of ZA should be evaluated in rats with normal renal function.The unavailability of some resources due to financial constricts were important obstacles in our study.

Conclusion
Our findings demonstrate that ZA administration at dose of (50 µg kg/week) showed efficacy against CCl 4 -induced RF through prevention of protein prenylation mainly by decreasing the expression of FPPS, FPP, and NF-κB.Consequently, there was a decrease in FPP, NF-Κb, oxidative stress (MDA), inflammation (TNF-α, and IL-6), apoptosis (caspase-3) and fibrosis (TGF-β and α-SMA) induced by CCl 4 in renal tissues.These data support the use of ZA in clinical trials to prevent RF.

Figure 1 .
Figure 1.Diagrammatic illustration of the study timeline for drug administration and timing of outcome measures.Wk week, MBP mean blood pressure, ZA zoledronate, CCl 4 carbon tetrachloride, i.p. intraperitoneal injection.

Figure 6 .
Figure 6.Caspase 3 Immunohistochemistry X400.(A) Control group: minimal reaction to caspase 3 in some tubular cells.(B) Model-RF Group: intense reaction to caspase 3 in most renal tubules.[(C) RF-ZA group: mild reaction to caspase 3 in some renal tubules.

Figure 8 .
Figure 8. α-SMA Immunohistochemistry X400.(A) Control group: minimal reaction to α-SMA in the wall of blood vessels (↑), negative reaction is seen in the renal glomeruli.(B) Model-RF group: intense reaction to α-SMA in the wall of blood vessels (↑) and inside the glomerulus (▲).(C) RF-ZA group: mild reaction to α-SMA in the wall of blood vessels (↑) and inside the glomerulus (▲).

Table 1 .
Effect of ZA (50 µg/kg/week) on MBP, kidney index, serum creatinine, BUN, uACR in a CCl 4 induced RF rat model.Data are mean ± S.D. n = 10 rats per group.ZA zoledronic acid, RF renal fibrosis, MBP mean blood pressure, uACR urinary albumin to creatinine ratio, BUN blood urea nitrogen.***P < 0.0001 significant compared to control group.### P < 0.0001 significant compared to model-RF group by one-way ANOVA with Tukey's multiple comparison test.