Manipulating Sirtuin 3 pathway ameliorates renal damage in experimental diabetes

More effective treatments for diabetic nephropathy remain a major unmet clinical need. Increased oxidative stress is one of the most important pathological mechanisms that lead to kidney damage and functional impairment induced by diabetes. Sirtuin 3 (SIRT3) is the main mitochondrial deacetylase and critically regulates cellular reactive oxygen species (ROS) production and detoxification. Honokiol is a natural biphenolic compound that, by activating mitochondrial SIRT3, can carry out anti-oxidant, anti-inflammatory and anti-fibrotic activities. Here, we sought to investigate the renoprotective effects of honokiol in BTBR ob/ob mice with type 2 diabetes. Diabetic mice were treated with vehicle or honokiol between the ages of 8 and 14 weeks. Wild-type mice served as controls. Renal Sirt3 expression was significantly reduced in BTBR ob/ob mice, and this was associated with a reduction in its activity and increased ROS levels. Selective activation of SIRT3 through honokiol administration translated into the attenuation of albuminuria, amelioration of glomerular damage, and a reduction in podocyte injury. SIRT3 activation preserved mitochondrial wellness through the activation of SOD2 and the restoration of PGC-1α expression in glomerular cells. Additionally, the protective role of SIRT3 in glomerular changes was associated with enhanced tubular Sirt3 expression and upregulated renal Nampt levels, indicating a possible tubule-glomerulus retrograde interplay, which resulted in improved glomerular SIRT3 activity. Our results demonstrate the hitherto unknown renoprotective effect of SIRT3 against diabetic glomerular disease and suggest that the pharmacological modulation of SIRT3 activity is a possible novel approach to treating diabetic nephropathy.


Results
SIRT3 is reduced in experimental diabetes, associates with increased ROS levels and is normalized by honokiol. To investigate whether SIRT3 plays a role in the pathogenesis of DN, we analyzed the gene expression of Sirt3 in the kidneys of BTBR WT and diabetic BTBR ob/ob mice. RT-PCR analysis showed that renal Sirt3 mRNA expression was markedly lower in BTBR ob/ob mice than that observed in WT mice (p < 0.001, Fig. 1a). Given that SOD2 is a major target of SIRT3 deacetylase activity, we measured the glomerular expression of acetylated SOD2 at Lysine 68, the specific residue regulated by SIRT3 21 . A greater expression of acetylated-SOD2 was detected in the glomeruli of BTBR ob/ob mice than in those of WT mice (p < 0.001), indicating lower SIRT3 deacetylase activity in the diabetic mice (Fig. 1b). If reduced SIRT3 activity is actually responsible for the inactivation of SOD2, we expected these changes to be paralleled by an increase in renal oxidative stress in diabetic mice. Indeed, immunohistochemical analysis showed that nitrotyrosine staining -a marker of peroxynitrite-mediated oxidative damage -was upregulated significantly in the glomerular cells of BTBR ob/ob mice compared to those of WT mice (Fig. 1c).
At this point we wondered whether the manipulation of the SIRT3 pathway with honokiol could have a renoprotective effect. Treatment with honokiol restored Sirt3 expression in BTBR ob/ob mice to levels comparable to BTBR WT mice (p < 0.05 versus vehicle, Fig. 1a). This effect was associated with a significant reduction in SOD2 acetylation in the glomeruli of treated BTBR ob/ob mice (p < 0.001 versus vehicle, Fig. 1b) and in nitrotyrosine expression (p < 0.001 versus vehicle, Fig. 1c). To rule out the possibility that the protective effect is mediated by SIRT3 and not shared by other sirtuins, we evaluated the expression of Sirt1 and Sirt6, as these are the most involved in renal disorders 15 . We found that the renal expression of Sirt1 was unchanged in diabetic mice (Fig. 1d) while Sirt6 was downregulated (Fig. 1e). Honokiol did not affect either Sirt1 or Sirt6 expression (Fig. 1d,e) suggesting selective activation of SIRT3.

Honokiol attenuates albuminuria and ameliorates glomerular injury.
To further examine the renoprotective effect of SIRT3 activation through honokiol treatment, we measured urinary albumin excretion and analyzed the histologic lesions in the kidney of BTBR ob/ob mice receiving vehicle or honokiol. We observed that 14-week-old vehicle BTBR ob/ob mice exhibited significantly higher levels of albuminuria than BTBR WT mice of the same age (p < 0.001). BTBR ob/ob mice treated with honokiol had a significantly lower albuminuria levels (p < 0.001) compared to mice receiving vehicle (Fig. 2a).
Diabetic BTBR ob/ob mice developed renal lesions consisting of mesangial matrix accumulation accompanied by mesangiolysis, resulting in disrupted sites where capillary loops are anchored into the mesangium, which leads to the dilation of the capillary loop (Fig. 2b). In association with mesangial matrix accumulation, the glomeruli of BTBR ob/ob mice on vehicle exhibited a glomerular capillary rarefaction (p < 0.001 versus WT mice), as revealed by immunofluorescence for CD31, a specific endothelial marker (Fig. 2c), and an increase in α-smooth muscle actin (α-SMA) expression (p < 0.001 versus WT mice), a marker of mesangial cell activation (Fig. 2d). Tubular damage in BTBR ob/ob mice was mild, as reported previously [18][19][20] . Honokiol treatment significantly (p < 0.001) limited mesangial matrix expansion and mesangiolysis (Fig. 2b). As shown in Fig. 2c, honokiol limited the decrease in CD31 staining (p < 0.05 versus BTBR ob/ob + vehicle), and glomerular α-SMA expression was also significantly (p < 0.001) lower in BTBR ob/ob mice after honokiol compared with vehicle (Fig. 2d).
Since recent studies have highlighted the critical role that SIRT3 plays in regulating the inflammatory response 22-24 , we investigated whether SIRT3-activating treatment with honokiol could reduce inflammation in diabetic mice. BTBR ob/ob mice that received vehicle exhibited a significantly greater accumulation of Mac-2-positive monocytes/macrophages at the glomerular level compared with BTBR WT mice (p < 0.001, Fig. 2e), and honokiol effectively reduced the number of glomerular Mac-2-positive infiltrating cells (p < 0.001 versus vehicle, Fig. 2e).
Honokiol did not affect major systemic alterations that had occurred in diabetic mice, such as increased body weight, hyperglycemia and dyslipidemia (Table 1). On the contrary, kidney weight, which had increased significantly in BTBR ob/ob mice receiving vehicle (p < 0.01 versus BTBR WT mice), was significantly lower after honokiol treatment (p < 0.05 versus vehicle) (Table 1).
By the end of the study period, the following mortality was recorded for the BTBR ob/ob mice: six out of twelve mice in the vehicle group died, while only three out of twelve mice in the honokiol group died. All BTBR WT control mice were alive.

Honokiol limits podocyte injury in diabetic mice.
To clarify what the cellular basis is for the observed reduction in albuminuria achieved by using honokiol in BTBR ob/ob mice, we examined the expression of nephrin -an essential component of the podocyte slit diaphragm that is crucial for maintaining slit pore integrity and renal filtration capacity 25 -and of nestin -a podocyte cytoplasmic protein that is involved in the organization of the cellular cytoskeleton and which plays an important role in maintaining normal podocyte function 26 . Immunofluorescence analyses showed intense nephrin and nestin signals with the typical epithelial-like staining Figure 1. Reduction of renal expression and activity of Sirt3 paralleled with an increase of ROS production in diabetic mice. (a) qRT-PCR analysis of Sirt3 mRNA levels at 14 weeks of age in kidney of BTBR wild-type (WT) mice (n = 9) and BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9) from 8 weeks of age. (b) Representative images and quantification of glomerular acetylated SOD2 staining in BTBR WT mice (n = 9) and in BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9) at 14 weeks of age. Insets show acetylated SOD2 in podocytes of WT and diabetic mice (arrowheads). Scale bars: 20 μm. (c) Representative images and quantification of glomerular nitrotyrosine staining in BTBR WT mice (n = 9) and in BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9) at 14 weeks of age. Insets show nitrotyrosine staining in podocytes of WT and diabetic mice (arrowheads). Scale bars: 20 μm. (d,e) qRT-PCR analysis of Sirt1 (d), and Sirt6 (e) mRNA levels in kidney of BTBR WT mice (n = 9) and BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9) at 14 weeks of age. Data are mean ± SEM and were analyzed by one-way ANOVA followed by Tukey's multiple comparisons test, *p < 0.05, ***p < 0.001 vs BTBR WT mice; # p < 0.05, ### p < 0.001 vs BTBR ob/ob + vehicle. pattern in the glomeruli of WT mice, while BTBR ob/ob mice receiving vehicle exhibited a consistent reduction and altered expression pattern for both markers (p < 0.001 versus WT mice, Fig. 3a,b). Honokiol treatment ameliorated the defective nephrin and nestin expression and pattern in diabetic mice (p < 0.001 versus vehicle Fig. 3a,b). and BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9). (b) Periodic acid-Schiff-stained sections of representative glomeruli and quantification from BTBR WT mice (n = 9) and from diabetic mice treated with vehicle (n = 6) or honokiol (n = 9) at 14 weeks of age showing glomerular lesions, consisting of mesangial matrix expansion (arrowheads) and mesangiolysis (asterisk). Scale bars: 20 μm. (c,d) Representative images and quantification of glomerular CD31 (c) and α-SMA expressions (d) in BTBR WT mice (n = 9) and in BTBR ob/ ob mice treated with vehicle (n = 6) or honokiol (n = 9) at 14 weeks of age. Nuclei were stained with DAPI and renal structure with lectin FITC-wheat germ agglutinin (WGA). Scale bars: 20 μm. (e) Representative images and quantification of glomerular accumulation of Mac-2-positive monocytes/macrophages in BTBR WT mice (n = 9) and in BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9) at 14 weeks of age. Scale bars: 20 μm. Data are mean ± SEM and were analyzed by one-way ANOVA followed by Tukey's multiple comparisons test, ***p < 0.001 vs BTBR WT mice; # p < 0.05, ### p < 0.001 vs BTBR ob/ob + vehicle. (2020) 10:8418 | https://doi.org/10.1038/s41598-020-65423-0 www.nature.com/scientificreports www.nature.com/scientificreports/ We then evaluated glomerular volume and podocyte number and density. Morphometric analysis of kidney sections revealed that glomerular volume increased in BTBR ob/ob mice that received vehicle (p < 0.001 versus WT mice, Fig. 3c). The number of WT1-positive podocytes per glomerulus was lower than in WT mice (p < 0.001), which translated into a significant reduction in podocyte density (p < 0.001, Fig. 3c). Honokiol reduced glomerular hypertrophy (p < 0.05 versus vehicle, Fig. 3c) and limited podocyte depletion (p < 0.05 versus vehicle, Fig. 3c).
Honokiol maintains mitochondrial homeostasis in the glomeruli of BTBR ob/ob mice. Given the role of SIRT3 in regulating mitochondrial structure and function, we investigated whether SIRT3 activation through honokiol translated into improvements in mitochondrial wellness. We therefore analyzed mitochondrial morphology using transmission electron microscopy. Podocytes of BTBR ob/ob mice given vehicle exhibited mitochondrial swelling that was associated with disarrangement of cristae, in contrast with the podocytes of WT mice with normal mitochondria morphology ( Fig. 4a,b). Honokiol treatment reversed mitochondria abnormalities induced by diabetes ( Fig. 4a,b).
To further assess the protective role of honokiol treatment, we investigated the expression of peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) -the master regulator of mitochondrial function 27,28 . We found that PGC-1α was significantly lower in the glomerular cells of diabetic mice (p < 0.001), while its expression was restored to control levels through treatment with honokiol (p < 0.01 versus vehicle, Fig. 4c).
Honokiol restores tubular expression of Sirt3. The modulation of total Sirt3 mRNA expression and its upregulation by honokiol in diabetic mice prompted us to assess Sirt3 mRNA localization in the kidney through in situ hybridization experiments. We found that Sirt3 was predominantly expressed in the tubular compartment of WT mice (Fig. 5a). In BTBR ob/ob mice given vehicle, the tubular expression of Sirt3 was significantly lower compared with WT mice (p < 0.05), but it was restored (p < 0.01 versus vehicle) through honokiol treatment (Fig. 5a,b). In contrast, a weak Sirt3 mRNA signal was found in the glomeruli of WT mice, which was not altered in either diabetic mice given vehicle or in those receiving honokiol (data not shown). To test whether increased Sirt3 mRNA levels, after honokiol treatment, were associated with its increased activity, we analyzed SOD2 acetylation status also in the tubules. Similar to the glomerular compartment, we observed an increased acetylation of SOD2 in the proximal tubules of BTBR ob/ob mice given vehicle, which was reduced in mice after honokiol treatment (p < 0.01 vs vehicle, Fig. 5c). To investigate whether the increased expression and activity of Sirt3 in tubular cells of honokiol-treated diabetic mice can contribute also to increased SIRT3 activity in the glomerular compartment, as it has been established with regard to SIRT1 29 , we evaluated the expression of nicotinamide phosphoribosyltransferase (NAMPT), the rate-limiting enzyme for the biosynthesis of nicotinamide adenine dinucleotide (NAD + ), the essential co-factor of SIRT3 activity. Our results showed that Nampt mRNA expression was significantly lower in the kidneys of BTBR ob/ob mice given vehicle than in those of WT mice (p < 0.05), and treatment with honokiol restored Nampt levels (p < 0.01 versus vehicle) in the diabetic mice (Fig. 5d).
In order to identify the potential mechanism through which honokiol treatment could promote SIRT3 expression and exert anti-oxidant activities, we investigated the expression of nuclear factor erythroid 2-related factor 2 (NRF2), the master regulator of anti-oxidant response [30][31][32] . As shown in Fig. 5e, we found that NRF2 protein expression was reduced in the nucleus and cytoplasm of BTBR ob/ob mice given vehicle compared to BTBR WT mice. Treatment with honokiol restored the expression of NRF2 (Fig. 5e). These data were confirmed by real time RT-PCR experiments that showed a significant reduction of Nrf2 in BTBR ob/ob mice given vehicle compared to BTBR WT mice (Fig. 5f). Treatment with honokiol normalized Nrf2 expression (Fig. 5f). Conversely, the expression of the NRF2 adaptor protein Keap1 was unchanged in any of the experimental groups (Fig. 5g), possibly suggesting that KEAP1 is not involved in the maintenance of the homeostatic levels of NRF2.

Discussion
In this study, we demonstrated that in experimental diabetes 1) renal SIRT3 expression and activity are reduced and are associated with increased oxidative stress; 2) selective manipulation of the SIRT3 pathway using honokiol protects against albuminuria, glomerular lesions and inflammation; 3) honokiol reduces podocyte damage and loss by preserving mitochondrial structure and function.
The first finding of this study is that Sirt3 mRNA expression was lower in the kidneys of BTBR ob/ob mice, which is in line with earlier observations in experimental type 1 diabetes 33 and in kidney biopsies from DN patients 16 . The reduction in Sirt3 expression in BTBR ob/ob mice was associated with an impairment in its deacetylase activity towards SOD2 and an increase in ROS levels. Oxidative stress is a well-known driver of www.nature.com/scientificreports www.nature.com/scientificreports/ diabetic kidney disease 5 , and in this regard our study shows that SIRT3-SOD2 axis is a critical modulator of renal oxidative stress in diabetic mice and that this molecular pathway could be targetable through honokiol. Indeed, we observed that honokiol enhanced Sirt3 mRNA levels in BTBR ob/ob mice, and this had a positive impact on SOD2 activity and oxidative stress. Previous studies have elegantly demonstrated that in the heart honokiol can enter mitochondria and physically bind to SIRT3, enhancing its affinity for NAD + with immediate consequences on deacetylase activity and ROS production 34 . However, whether honokiol's action is exclusively directed towards the activation of SIRT3 and not shared with other sirtuins has not been addressed in these studies. The finding here that honokiol did not modulate the renal expression of either Sirt1 or Sirt6, which are, along with SIRT3, involved in kidney disease progression 15 , clearly demonstrates the beneficial effects of honokiol on the selective restoration of SIRT3 in the kidney. and in BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9) at 14 weeks of age. (c) Representative images and morphometric analysis of glomerular volume, WT1-positive podocytes, expressed as number per glomerulus, and podocyte density in BTBR WT mice (n = 9) and in BTBR ob/ob mice treated with vehicle (n = 6) and honokiol (n = 9) at 14 weeks of age. Scale bars: 20 μm. Data are mean ± SEM and were analyzed by one-way ANOVA followed by Tukey's multiple comparisons test, ***p < 0.001 vs BTBR WT mice; # p < 0.05, ### p < 0.001 vs BTBR ob/ob + vehicle. Improvements in albuminuria and glomerular damage after treatment of BTBR ob/ob mice with honokiol appear to be relatively consistent. Furthermore, the large reduction in glomerular inflammation we observed in these mice demonstrates that SIRT3 has a potent anti-inflammatory effect on the diabetic kidney that has never been reported before. Glomerular hypertrophy has been identified as a characteristic feature of diabetic glomerular injury in experimental models and in humans. This is accompanied by the inability of podocytes to maintain complete coverage of the glomerular filtration surface area, which results in podocyte hypertrophic stress, leading to podocyte detachment 35 . Podocytes are critical players in maintaining the integrity of the glomerular filtration barrier, and podocyte injury and loss have been identified as the initial event in the development of proteinuria and glomerular lesions, ending in glomerulosclerosis. The evidence indicates that the podocyte is the earliest target of diabetic injury, and indeed podocyte number correlates with albuminuria, and glomerular podocyte density appears to be one of the best predictors of albuminuria and disease progression 36 . In this study, the anti-albuminuric effect of honokiol was associated with an amelioration of the defective expression of podocyte proteins and a reduction in podocyte loss in BTBR ob/ob mice. Increasing evidence indicates that the disruption of mitochondrial bioenergetics in podocytes is crucial for dictating the development and progression of DN [37][38][39] , and recent findings have provided novel correlations between podocyte mitochondrial morphology and the progression of DN 40,41 . Here, treatment with honokiol improved podocyte mitochondrial abnormalities in diabetic mice and also restored the expression of PGC-1α, a known modulator of mitochondrial homeostasis, thereby reinforcing the hypothesis that increasing SIRT3 activity is crucial in the preservation of mitochondrial integrity 42,43 . According to a recent study 44 , it is conceivable that the ability of honokiol to modulate PGC-1α could be dependent on the activation of the AMPK-CREB pathway by SIRT3, ultimately resulting in PGC-1α stimulation.
To further investigate the mechanisms underlying honokiol-induced SIRT3 activation in DN in greater depth, we analyzed the localization of Sirt3 expression in the kidneys of BTBR ob/ob mice. We observed that Sirt3 levels in tubular cells were lower in diabetic mice and were restored by honokiol treatment, accompanied by a reduction www.nature.com/scientificreports www.nature.com/scientificreports/ in the acetylation of the SIRT3 target SOD2. The possible mechanism through which honokiol stimulates SIRT3 protein expression relies on NRF2 that we found increased in the kidney of treated diabetic mice. That NRF2 can upregulate SIRT3 expression is supported by the evidence that NRF2 induces SIRT3 expression through the direct binding of NRF2 subunit to the SIRT3 promoter 45 . Representative images (a) and quantification (b) of in situ hybridization for Sirt3 in kidney cortex from BTBR WT mice and BTBR ob/ob mice treated with vehicle or honokiol at 14 weeks of age. Scale bars: 20 μm. Insets show the localization of Sirt3 in tubular cells. Image-based quantitative software analysis was performed to evaluate tubular expression of Sirt3. Fiji Image J software (https://imagej.net/Fiji) was used for the quantification of the number of Sirt3 mRNA dots (representing single mRNA molecules). Orbit Image analysis software (http:// orbit.bio) was used to count the number of cells. Sirt3 mRNA levels were expressed as average number of dots per cell. (c) Quantification of tubular acetylated SOD2 staining in BTBR WT mice (n = 9) and in BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9) at 14 weeks of age. (d) qRT-PCR analysis of Nampt mRNA levels in kidney of BTBR WT mice (n = 9) and BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9). (e) Representative images of NRF2 expression in BTBR WT mice (n = 9) and in BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9) at 14 weeks of age. Scale bars: 50 μm. (f,g) qRT-PCR analysis of Nrf2 (f) and Keap1 (g) mRNA levels in kidney of BTBR WT mice (n = 9) and BTBR ob/ob mice treated with vehicle (n = 6) or honokiol (n = 9). Data are mean ± SEM and were analyzed by one-way ANOVA followed by Tukey's multiple comparisons test, *p < 0.05, ***p < 0.001 vs BTBR WT mice; ## p < 0.01 vs BTBR ob/ob + vehicle.

Scientific RepoRtS |
(2020) 10:8418 | https://doi.org/10.1038/s41598-020-65423-0 www.nature.com/scientificreports www.nature.com/scientificreports/ On the other hand, we found that Sirt3 expression was not modulated by honokiol in the glomeruli of BTBR ob/ob mice. These results reminded us of those reported in an interesting study by Hasegawa et al. 29 , in which the selective upregulation of tubular SIRT1 mediated a retrograde interplay between tubules and podocytes, which resulted in the amelioration of diabetes-associated glomerular disease. In that study, the authors reported that the upregulation of NAMPT in tubular cells, mediated by increased SIRT1 levels, maintained adequate nicotinamide mononucleotide (NMN) concentrations around glomeruli to promote podocyte function, ultimately translating into an anti-albuminuric effect in diabetes. NAMPT is also a critical regulator of SIRT3 activity, as it produces NMN, the intermediate product for NAD + biosynthesis 46,47 . Consistent with the interpretation provided by Hasegawa 29 we suggest that the protective effect of SIRT3 on albuminuria and glomerular changes in BTBR ob/ob mice could be due to tubule-glomerulus retrograde interplay. In particular, the upregulation of SIRT3 and NAMPT in tubular cells may provide the required amount of NMN to diabetic podocytes and other glomerular cells, ultimately supplying glomerular NAD + to further increase SIRT3 activity in a virtuous cycle.
In conclusion, here we have shown that SIRT3 plays a crucial role in the pathogenesis of DN and that its specific activation through honokiol reduces diabetes-induced oxidative stress and protects podocytes and, generally, the glomerulus from diabetes-induced damage. In the context of the great interest that antioxidant therapies have generated, as promising treatments for DN and other chronic diabetic complications 48 , our data provide evidence of a hitherto unknown protective effect of SIRT3 against diabetic glomerular disease. This suggests that the pharmacological activation of SIRT3 activity may be an effective, novel approach for treating DN.

Methods
Experimental design. Male BTBR (black and tan, brachyuric) Lep ob/ob and BTBR wild-type (WT) mice were obtained from Jackson Laboratories (Bar Harbor, ME, USA) and were kept on specific pathogen-free facility with constant temperature on a 12:12-hour light-dark cycle with free access to standard diet and water. At 8 weeks of age, when they had already developed albuminuria, BTBR ob/ob mice were randomly allocated to receive (n = 12 mice/group): vehicle (DMSO in saline solution) or honokiol (10 mg/kg in DMSO; BioVision, Milpitas, CA, USA) by once-daily intraperitoneal injection. The dose of honokiol was chosen according to available data in the literature 49 . Treatment lasted until mice were 14 weeks old. BTBR WT mice (n = 9) were followed for the same length of time as controls. Mice were euthanized through CO 2 inhalation and their kidneys were collected and processed for analysis. Before sacrifice, mice were housed in metabolic cages for 24-hour urine collection for albuminuria assessment. Blood samples were collected for glucose, cholesterol and triglyceride measurements. The experimenters were not blind to the treatment, but they were blind for measurement of experimental outcomes. All animal experiments were conducted in accordance with institutional guidelines in compliance with national (D.L.n. 26, March 4, 2014), and international laws and policies (directive 2010/63/EU on the protection of animals used for scientific purposes) and were approved by the Institutional Animal Care and Use Committees of Istituto di Ricerche Farmacologiche Mario Negri IRCCS.
Biochemical parameters. Biochemical parameters were assessed as we previously described 20 Quantitative (q) RT-PCR. Total RNA was isolated from whole kidney tissue as we previously described 51 .
Renal histology. Kidney samples were fixed in Duboscq-Brazil (catalog P0094, Diapath, Bergamo, Italy), dehydrated, and embedded in paraffin, as we previously described 50 . Three-micrometer sections were stained with periodic acid-Schiff (PAS) reagent, and at least 50 glomeruli were examined per animal. The degree of glomerular mesangial matrix expansion was quantified using a score between 0 and 3 (0 = no mesangial matrix expansion; 1 = minimal; 2 = moderate; 3 = diffuse mesangial matrix expansion). The number of glomeruli exhibiting mesangiolysis in an entire kidney section was counted and expressed as a percentage. All biopsies were reviewed by a blinded pathologist. Samples were examined using ApoTome Axio Imager Z2 (Zeiss, Jena, Germany).

Immunohistochemistry.
For immunoperoxidase experiments, as we previously performed 50 , formalin-fixed, 3-μm paraffin-embedded kidney sections were incubated with Peroxidazed 1 (catalog PX968H, Biocare Medical, (2020) 10:8418 | https://doi.org/10.1038/s41598-020-65423-0 www.nature.com/scientificreports www.nature.com/scientificreports/ isomerase B) and the bacterial gene DapB were used as positive and negative controls, respectively. Sirt3 mRNA molecules were visualized as brown, punctate dots. Ten fields of tubule cells and twenty glomeruli for each animal were randomly acquired using bright-field microscopy (ApoTome, Axio Imager Z2, Zeiss). Image-based quantitative software analysis was performed to evaluate tubular and glomerular expression of Sirt3. Fiji Image J software (https://imagej.net/Fiji) was used for the quantification of the number of Sirt3 mRNA dots (representing single mRNA molecules). Orbit Image analysis software (https://orbit.bio) was used to count the number of cells. Sirt3 mRNA levels were expressed as average number of dots per cell.

Statistical analysis.
Results were expressed as mean ± SEM and in bar chart with individual data points.
Data analysis was performed using Graph Pad Prism software (Graph Pad, San Diego, CA, USA). Comparisons were made using one-way ANOVA with Tukey's multiple comparisons post hoc test, and the statistical significance was defined as a p value of <0.05.

Data availability
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.