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Amorphophallus campanulatus tuber extract protects diabetic nephropathy in streptozotocin-induced diabetic nephropathy rat model by regulating oxidative stress and TNF-α inflammatory pathway

ABSTRACT

Purpose:

To assess the effect of Amorphophallus campanulatus tuber (Ac) extract in the protection of diabetic nephropathy in streptozotocin (STZ) induced diabetic nephropathy (DN) rat model.

Methods:

Diabetes was induced with STZ (60 mg/kg, i.p.), and DN was confirmed after six weeks of STZ administration with the estimation of kidney function test. Further rats were treated with Ac 250 and 500 mg/kg p.o. for next four week. Oxidative stress and level of inflammatory cytokines were estimated in the kidney tissue of DN rats. Histopathology of kidney tissue was performed using hematoxylin and eosin staining.

Results:

There was improvement in the body weight of Ac treated groups than DN group of rats. Blood glucose level was observed to be reduced in Ac treated groups than DN group on 42nd and 70th day of protocol. Treatment with Ac ameliorated the altered level of kidney function tests (creatinine and BUN), enzymes of liver function (aspartate aminotransferase and alanine aminotransferase), and lipid profile in the serum of DN rats. Oxidative stress parameters (malondialdehyde and reactive oxygen species enhances and reduction in the level of glutathione and superoxide dismutase) and inflammatory cytokines such as interleukin-6, tumour necrosis factor-α, and monocyte chemoattractant protein-1 reduces in the tissue of Ac treated group than DN group. Treatment with Ac also attenuates the altered histopathological changes in the kidney tissue of DN rats.

Conclusions:

The report suggests that Ac protects renal injury in DN rats by regulating inflammatory cytokines and oxidative stress.

Key words
Diabetic Nephropathies; Streptozotocin; Oxidative Stress; Inflammation

Introduction

Diabetes mellitus in long-term development of several complications causes dysfunction of different organs like impairment of kidney function known as diabetic nephropathy (DN)11 Dabla PK. Renal function in diabetic nephropathy. World J Diabetes. 2010;1(2):48-56. https://doi.org/10.4239/wjd.v1.i2.48
https://doi.org/10.4239/wjd.v1.i2.48...
. Prevalence of DN found to be very high between 30–40%, which is the major cause of the end-stage kidney disease throughout the globe22 Gheith O, Farouk N, Nampoory N, Halim MA, Al-Otaibi T. Diabetic kidney disease: world wide difference of prevalence and risk factors. J Nephropharmacol. 2015;5(1):49-56. . Structural and functional abnormality of kidney are the characteristics of DN, development of it reported to be occurs due to accumulation of advanced glycation end products (AGEs), inflammation, oxidative stress, and changes in renal hemodynamic due to uncontrolled hyperglycaemia33 Mallipattu SK, Uribarri J. Advanced glycation end product accumulation: a new enemy to target in chronic kidney disease? Curr Opin Nephrol Hypertens. 2014;23(6):547-54. https://doi.org/10.1097%2FMNH.0000000000000062
https://doi.org/10.1097%2FMNH.0000000000...
,44 Tripathi AS, Mazumder PM, Chandewar AV. Changes in the pharmacokinetic of sildenafil citrate in rats with Streptozotocin-induced diabetic nephropathy. J Diabetes Metab Disord. 2014;13(1):8. https://doi.org/10.1186%2F2251-6581-13-8
https://doi.org/10.1186%2F2251-6581-13-8...
. Production of reactive oxygen species (ROS) enhances in oxidative stress, which enhances the production of AGE, and its deposition promotes injury to kidney tissue55 Kim J, Seok YM, Jung KJ, Park KM. Reactive oxygen species/oxidative stress contributes to progression of kidney fibrosis following transient ischemic injury in mice. Am J Physiol Renal Physiol. 2009;297(2):F461-70. https://doi.org/10.1152/ajprenal.90735.2008
https://doi.org/10.1152/ajprenal.90735.2...
. Moreover, inflammatory cytokines such as tumour necrosis factor (TNF)-α and interleukin (IL)-6 altered the renal function, which also activates oxidative mechanism progress into DN66 Donate-Correa J, Martín-Núñez E, Muros-de-Fuentes M, Mora-Fernández C, Navarro-González JF. Inflammatory cytokines in diabetic nephropathy. J Diabetes Res. 2015;2015:948417. https://doi.org/10.1155/2015/948417
https://doi.org/10.1155/2015/948417...
. Chemical constituents inhibit the progression of development of DN by attenuating the altered inflammatory and oxidative pathway.

Herbs are used as a complimentary medicine for the management of several chronic disorder. Amorphophallus campanulatus (Roxb.) Bl. belongs to Araceae family and is traditionally used for the management of tumours, piles, liver diseases, and abdominal pain. Amorphophallus campanulatus (AC) tuber is reported for immunomodulatory, central nervous system depressant, cytotoxicity, antifungal, antibacterial, analgesic, and antiprotease activity77 Tripathi AS, Chitra V, Sheikh NW, Mohale DS, Dewani AP. Immunomodulatory Activity of the Methanol Extract of Amorphophallus campanulatus (Araceae) Tuber. Trop J Pharm Res. 2010;9(5):451-54. https://doi.org/10.4314/tjpr.v9i5.61055
https://doi.org/10.4314/tjpr.v9i5.61055...
1010 Ansil PN, Wills PJ, Varun R, Latha MS. Cytotoxic and apoptotic activities of Amorphophallus campanulatus tuber extracts against human hepatoma cell line. Res Pharm Sci. 2014;9(4):269-77. . Moreover, AC has strong antidiabetic activity, which reduces blood glucose level by regulating TNF-α1111 Setyawati I. Suweg Flour (Amorphophallus Campanulatus) Potential Reducing TNF-α Levels in Model Diabetic Rats. Mutiara Medika. 2020;20(2):56-61. https://doi.org/10.18196/mm.200246
https://doi.org/10.18196/mm.200246...
. There are several phytochemicals such as sterols, terpenoids, coumarins, alkaloid, and flavonoids, specifically 3,5-diacetylambulin and Amblyone identified in AC tuber1212 Dey YN, Ota S, Srikanth N, Jamal M, Wanjari M. A phytopharmacological review on an important medicinal plant - Amorphophallus paeoniifolius. Ayu. 2012;33(1):27-32. https://doi.org/10.4103%2F0974-8520.100303
https://doi.org/10.4103%2F0974-8520.1003...
. These phytochemicals are also known to have beneficial effects on health. Thus, the present investigation evaluated the protective effect of AC against DN.

Methods

Animals

Wistar rats (gender: male; age: 12 weeks old; weight: 200–230 g) were housed under controlled condition such as humidity: ~60%, temperature: 25 ± 2ºC and 12-h light/dark cycle. All the experimental protocol was approved on July 15, 2018 by the institutional animal ethical committee (650/02/C/CPCSEA/2/2014).

Procurement and extraction Amorphophallus campanulatus

Amorphophallus campanulatus tubers were cut into small pieces and dried under the shade. Thereafter, we coarsely powdered it with the help of a grinder, maceration was performed by placing the powder into methanol for five days, and we shook it at a regular interval. Vacuum evaporation was performed to obtain the extract, percentage yield was found to be 11.5% w/w. Preliminary phytochemical screening revealed the presence of flavonoids, tannins, and sterols in the methanolic extract.

Induction of diabetic nephropathy

Diabetes was induced in all the group of rats excluding control group by the single dose administration of streptozotocin (STZ) (60 mg/kg, i.p.)1313 Tripathi AS, Mazumder PM, Chandewar AV. Evaluation of drug interaction of glimepiride with phosphodiesterase inhibitors type V in diabetic nephropathy. Exp Clin Endocrinol Diabetes. 2014;122(10):597-601. https://doi.org/10.1055/s-0034-1382034
https://doi.org/10.1055/s-0034-1382034...
. Blood glucose level was estimated in the serum of these rats after 72 hours of STZ administration for the confirmation of the diabetes. Glucose level more than 200 mg/dL was considered to be diabetic. All the rats were kept for six weeks, and kidney function was estimated at the end of each week for the confirmation of DN.

All the animals were grouped into four different parts – control group; DN group; AC 250 mg/kg and 500 mg/kg. The last two groups receiveed methanolic extract of AC tubers at the doses of 250 and 500 mg/kg p.o. for four weeks. Blood glucose level and body weight of each rat were estimated every week due the protocol.

Assessment of kidney function

Kidney function was estimated by determining the biochemical level such as creatinine, BUN and lipid profile in the serum of all the groups of rats using their respective kits.

Assessment of oxidative stress parameters

Phosphate buffer was used to homogenate the tissue sample by centrifuging it for the period of 15 min at 12,000×. Level of malondialdehyde (MDA) and activity of glutathione (GSH) and superoxide dismutase (SOD) were determined in the tissue homogenate as per the instruction of manufacturer using spectrophotometer. Moreover, level of ROS generation was also estimated as per the direction given by the manufacturer of the kit.

Assessment of cytokine

Kidney tissue isolated from each rat was homogenized under phosphate buffer, and level of TNF-α, IL-6 and monocyte chemoattractant protein-1 (MCP-1) were estimated in the tissue homogenate of kidney of rats using enzyme-linked immunosorbent assay (ELISA) method.

Assessment of histopathology of kidney tissue

Kidney was isolated from each animal and fixed with the help of 10% formalin solution. Further, kidney tissue was dehydrated with different concentration of ethanol and seed into molten paraffin wax to prepare wax cubes. Tissue was sectioned with the help of microtome, having 5-µm thickness, and stained with hematoxylin and eosin (H&E) staining. Assessment was performed using trinocular microscope.

Statistical analysis

The report is represented by mean ± standard error of the mean (SEM), and GraphPad prism software version 9.3.1. (471) was used for statistical analysis with one-way analysis of variance. Significance level was considered as p < 0.05.

Results

Effect of Amorphophallus campanulatus on body weight

Bodyweight was estimated in the AC treated STZ induced DN rats, as shown in Fig. 1. There was significant decrease in the body weight of STZ induced DN groups than control group for six weeks. In DN group, body weight was observed to be further reduced till the end of protocol than control group of rats. There was significant improvement in the body weight of AC treated group than DN group of rats.

Figure 1
Assessment of the effect of Amorphophallus campanulatus on the body weight of streptozotocin induced diabetic nephropathic (DN) rats. Mean ± standard error of the mean (n = 6).

Effect of Amorphophallus campanulatus on the level of blood glucose

Blood glucose level was estimated in the serum of AC treated DN rats on the third, 42nd and 70th day of protocol, as shown in Fig. 2. Administration STZ enhanced the level of glucose in the serum of all the groups than control group of rats on the third day of protocol, and it remained higher till the end of the 42nd day of study. Further, level of glucose enhanced in the serum of DN group than control group of rats, which was reversed in AC treated group in a dose-dependent manner.

Figure 2
Assessment of the effect of Amorphophallus campanulatus on level of glucose in the serum of streptozotocin induced diabetic nephropathic (DN) rats. Mean ± standard error of the mean (n = 6).

Effect of Amorphophallus campanulatus on the biochemical parameters

Biochemical parameters were estimated in the serum of AC treated STZ induced DN rats. Levels of creatinine, BUN, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were enhanced significantly in the serum of DN group than control group. AC treated group showed significant reduction in the level of these biochemical parameters in a dose-dependent manner in the serum than DN group of rats (Fig. 3).

Figure 3
Assessment of the effect of Amorphophallus campanulatus on the biochemical parameters in the serum of streptozotocin induced diabetic nephropathic (DN) rats. Mean ± standard error of the mean (n = 6).

Effect of Amorphophallus campanulatus on the lipid profile

Lipid profile was observed in the serum of AC treated STZ induced DN rats. Level of total cholesterol (TC), triglycerides (TG) and low-density lipoprotein (LDL) enhanced, and reduction in the level of high-density lipoprotein (HDL) was observed in the serum of DN group than control group of rats. Treatment with AC ameliorated the altered profile of lipid in the serum of STZ induced DN rats (Fig. 4).

Figure 4
Assessment of the effect of Amorphophallus campanulatus on the lipid profile of streptozotocin induced diabetic nephropathic (DN) rats. Mean ± standard error of the mean (n = 6).

Effect of Amorphophallus campanulatus on oxidative stress parameters

Oxidative stress was estimated by determining level of its parameters in the kidney tissue of DN rats. Level of MDA and ROS enhanced, and reduction in the level of GSH and SOD were observed in the tissue of DN group than control group of rats. Treatment with AC attenuated the altered parameters of oxidative stress in the kidney tissue of DN rats (Fig. 5).

Figure 5
Assessment of the effect of Amorphophallus campanulatus on oxidative stress parameters in the kidney tissue of streptozotocin induced diabetic nephropathic (DN) rats. Mean ± standard error of the mean (n = 6).

Effect of Amorphophallus campanulatus on inflammatory cytokines

Mediators of inflammation like IL-6, TNF-α, and MCP-1 were estimated in the kidney tissue of DN rats, as shown in Fig. 6. In DN group, level of mediators of cytokines enhanced in the kidney tissue than control group. These mediators were reduced significantly in AC treated group than DN group of rats in a dose-dependent manner.

Figure 6
Assessment of effect of Amorphophallus campanulatus on mediators of inflammation in the kidney tissue of streptozotocin induced diabetic nephropathic (DN) rats. Mean ± standard error of the mean (n = 6).

Effect of Amorphophallus campanulatus on histopathological changes

Histopathological changes were estimated in the kidney tissue of AC treated DN rats by using H&E staining. Section of kidney tissue of control group showed normal appearance of morphology of glomerulus and tubules. DN group showed inflammatory changes in the kidney tissue, glomerular sclerosis, infiltration of lymphocytes, and degenerative changes in the nephrons. These changes reverse and histopathology of kidney tissue appeared to be normal in AC treated group of rats (Fig. 7).

Figure 7
Assessment of the effect of Amorphophallus campanulatus on the histopathological changes in kidney tissue of streptozotocin induced diabetic nephropathic (DN) rats (n = 6).

Discussion

Diabetes is a disorder of glucose metabolism that promotes serum concentration of blood glucose, which involves alteration of lipid profile1414 Tripathi AS, Mazumder PM, Chandewar AV. Sildenafil, a phosphodiesterase type 5 inhibitor, attenuates diabetic nephropathy in STZ-induced diabetic rats. J Basic Clin Physiol Pharmacol. 2016;27(1):57-62. https://doi.org/10.1515/jbcpp-2015-0035
https://doi.org/10.1515/jbcpp-2015-0035...
. It contributes to the enhancement of lipid level in the serum of diabetic rats, which develops atherosclerosis leading to diabetic complications including DN1313 Tripathi AS, Mazumder PM, Chandewar AV. Evaluation of drug interaction of glimepiride with phosphodiesterase inhibitors type V in diabetic nephropathy. Exp Clin Endocrinol Diabetes. 2014;122(10):597-601. https://doi.org/10.1055/s-0034-1382034
https://doi.org/10.1055/s-0034-1382034...
. Clinically, patients suffering from DN shows increase in blood glucose and reduction in body weight1515 Knowler WC, Barrett-Connor E, Fowler SE, Hamman RF, Lachin JM, Walker EA, Nathan DM; Diabetes Prevention Program Research Group. Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. N Engl J Med. 2002;346(6):393-403. https://doi.org/10.1056/nejmoa012512
https://doi.org/10.1056/nejmoa012512...
, which is supported by our study. Literature reveals that reduction in blood glucose level ceases the reduction in body weight1616 Schwartz SS, Kohl BA. Glycemic control and weight reduction without causing hypoglycemia: the case for continued safe aggressive care of patients with type 2 diabetes mellitus and avoidance of therapeutic inertia. Mayo Clin Proc. 2010;85(12 Suppl.):S15-26. https://doi.org/10.4065/mcp.2010.0468
https://doi.org/10.4065/mcp.2010.0468...
. AC is reported to possess antidiabetic activity as it reduces level of blood glucose in diabetic rats11. Data of study suggest that treatment with AC reduces the blood glucose and promotes the body weight in DN rats.

DN is one of the major chronic complications of diabetes. Several pathogenic pathways is involved in its development, including increase in lipid level that promotes injury to nephrons. Clinical study depicts the increase in creatinine and BUN level in the serum of DN patients1717 Dejenie TA, Abebe EC, Mengstie MA, Seid MA, Gebeyehu NA, Adella GA, Kassie GA, Gebrekidan AY, Gesese MM, Tegegne KD, Anley DT, Feleke SF, Zemene MA, Dessie AM, Moges N, Kebede YS, Bantie B, Adugna DG. Dyslipidemia and serum cystatin C levels as biomarker of diabetic nephropathy in patients with type 2 diabetes mellitus. Front Endocrinol (Lausanne). 2023;14:1124367. https://doi.org/10.3389/fendo.2023.1124367
https://doi.org/10.3389/fendo.2023.11243...
. These biochemicals are considered as the markers of renal failure, and an increase in the level of these markers deemed to be clinical feature of renal injury. Reduction in the level of these biochemical parameters of kidney function in the serum mean the protection of renal injury1818 Lopez-Giacoman S, Madero M. Biomarkers in chronic kidney disease, from kidney function to kidney damage. World J Nephrol. 2015;4(1):57-73. https://doi.org/10.5527/wjn.v4.i1.57
https://doi.org/10.5527/wjn.v4.i1.57...
, which was supported by this study, as AC treated group showed reduced level of BUN and creatinine in the serum of DN rats.

Lipid profile alters in DN, as LDL, TC and TG level enhances and HDL level reduces in DN. This altered level of lipid profile, specifically increased levels of LDL, promotes oxidative stress in the nephron tissue1919 Vaziri ND. Disorders of lipid metabolism in nephrotic syndrome: mechanisms and consequences. Kidney Int. 2016;90(1):41-52. https://doi.org/10.1016/j.kint.2016.02.026
https://doi.org/10.1016/j.kint.2016.02.0...
. MDA is one of the major markers of oxidative stress, known to enhance its level in nephropathy. Production of ROS enhances in due to alteration in the lipid level, which promotes the production of superoxide anions2020 Su LJ, Zhang JH, Gomez H, Murugan R, Hong X, Xu D, Jiang F, Peng ZY. Reactive Oxygen Species-Induced Lipid Peroxidation in Apoptosis, Autophagy, and Ferroptosis. Oxid Med Cell Longev. 2019;2019:5080843. https://doi.org/10.1155/2019/5080843
https://doi.org/10.1155/2019/5080843...
. These superoxide anions failed to be digested by SOD, leading to alterations in the integrity of cell membrane. MDA is a content of cell membrane due to injury to it, and the release of MDA in the serum causes increase in the level of MDA. These changes could appear due to the reduction in the level of GSH and SOD and increase in production of ROS2121 Nita M, Grzybowski A. The Role of the Reactive Oxygen Species and Oxidative Stress in the Pathomechanism of the Age-Related Ocular Diseases and Other Pathologies of the Anterior and Posterior Eye Segments in Adults. Oxid Med Cell Longev. 2016;2016:3164734. https://doi.org/10.1155/2016/3164734
https://doi.org/10.1155/2016/3164734...
. The study revealed that treatment with AC ameliorates the altered lipid profile and oxidative stress parameters in the serum and kidney tissue homogenate of DN rats, respectively. These changes in lipid profile and oxidative stress of AC shows the protective effect of it against DN.

Damage to the cell membrane of nephrons activates the inflammatory pathway, as it promotes infiltration of lymphocytes, which further contributes in the development of injury to nephrons2222 Imig JD, Ryan MJ. Immune and inflammatory role in renal disease. Compr Physiol. 2013;3(2):957-76. https://doi.org/10.1002/cphy.c120028
https://doi.org/10.1002/cphy.c120028...
. Inflammatory mediators like TNF-α and IL-6 are the majorly cytokines involved in injury to nephrons, and infiltration of lymphocytes due to increase in MCP-1 and regulation in the level of these mediators promotes injury to nephrons2323 Cantero-Navarro E, Rayego-Mateos S, Orejudo M, Tejedor-Santamaria L, Tejera-Muñoz A, Sanz AB, Marquez-Exposito L, Marchant V, Santos-Sanchez L, Egido J, Ortiz A, Bellon T, Rodrigues-Diez RR, Ruiz-Ortega M. Role of Macrophages and Related Cytokines in Kidney Disease. Front Med (Lausanne). 2021;8:688060. https://doi.org/10.3389%2Ffmed.2021.688060
https://doi.org/10.3389%2Ffmed.2021.6880...
. Data of given report suggest that treatment with AC reduces the level of these mediators to protect the renal injury in DN rats. Moreover, histopathology study also revealed that treatment with AC reverses the histopathological changes in the kidney tissue of DN rats.

Conclusion

The present study shows the protective effect of AC against DN, as it regulates level of oxidative stress and inflammatory pathway in STZ induced DN rats. Results shows AC could be used clinically for the management of DN.

Acknowledgements

All the author of the study are thankful to The Third Affiliated Hospital of Air Force Medical University, China, for providing the necessary facility.

  • Research performed at Postgraduate Program of Nephrology, Air Force Medical University, Xi’an, China. Tutor: Xiaoying Li.
  • Funding

    Not applicable.

Data availability statement

All data generated or analyzed during this study are included in this article.

References

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    Dabla PK. Renal function in diabetic nephropathy. World J Diabetes. 2010;1(2):48-56. https://doi.org/10.4239/wjd.v1.i2.48
    » https://doi.org/10.4239/wjd.v1.i2.48
  • 2
    Gheith O, Farouk N, Nampoory N, Halim MA, Al-Otaibi T. Diabetic kidney disease: world wide difference of prevalence and risk factors. J Nephropharmacol. 2015;5(1):49-56.
  • 3
    Mallipattu SK, Uribarri J. Advanced glycation end product accumulation: a new enemy to target in chronic kidney disease? Curr Opin Nephrol Hypertens. 2014;23(6):547-54. https://doi.org/10.1097%2FMNH.0000000000000062
    » https://doi.org/10.1097%2FMNH.0000000000000062
  • 4
    Tripathi AS, Mazumder PM, Chandewar AV. Changes in the pharmacokinetic of sildenafil citrate in rats with Streptozotocin-induced diabetic nephropathy. J Diabetes Metab Disord. 2014;13(1):8. https://doi.org/10.1186%2F2251-6581-13-8
    » https://doi.org/10.1186%2F2251-6581-13-8
  • 5
    Kim J, Seok YM, Jung KJ, Park KM. Reactive oxygen species/oxidative stress contributes to progression of kidney fibrosis following transient ischemic injury in mice. Am J Physiol Renal Physiol. 2009;297(2):F461-70. https://doi.org/10.1152/ajprenal.90735.2008
    » https://doi.org/10.1152/ajprenal.90735.2008
  • 6
    Donate-Correa J, Martín-Núñez E, Muros-de-Fuentes M, Mora-Fernández C, Navarro-González JF. Inflammatory cytokines in diabetic nephropathy. J Diabetes Res. 2015;2015:948417. https://doi.org/10.1155/2015/948417
    » https://doi.org/10.1155/2015/948417
  • 7
    Tripathi AS, Chitra V, Sheikh NW, Mohale DS, Dewani AP. Immunomodulatory Activity of the Methanol Extract of Amorphophallus campanulatus (Araceae) Tuber. Trop J Pharm Res. 2010;9(5):451-54. https://doi.org/10.4314/tjpr.v9i5.61055
    » https://doi.org/10.4314/tjpr.v9i5.61055
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    Dey YN, Sharma G, Wanjari MM, Kumar D, Lomash V, Jadhav AD. Beneficial effect of Amorphophallus paeoniifolius tuber on experimental ulcerative colitis in rats. Pharm Biol. 2017;55(1):53-62. https://doi.org/10.1080%2F13880209.2016.1226904
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    Jain S, Dixit VK, Malviya N, Ambawatia V. Antioxidant and hepatoprotective activity of ethanolic and aqueous extracts of Amorphophallus campanulatus Roxb. tubers. Acta Pol Pharm. 2009;66(4):423-8.
  • 10
    Ansil PN, Wills PJ, Varun R, Latha MS. Cytotoxic and apoptotic activities of Amorphophallus campanulatus tuber extracts against human hepatoma cell line. Res Pharm Sci. 2014;9(4):269-77.
  • 11
    Setyawati I. Suweg Flour (Amorphophallus Campanulatus) Potential Reducing TNF-α Levels in Model Diabetic Rats. Mutiara Medika. 2020;20(2):56-61. https://doi.org/10.18196/mm.200246
    » https://doi.org/10.18196/mm.200246
  • 12
    Dey YN, Ota S, Srikanth N, Jamal M, Wanjari M. A phytopharmacological review on an important medicinal plant - Amorphophallus paeoniifolius Ayu. 2012;33(1):27-32. https://doi.org/10.4103%2F0974-8520.100303
    » https://doi.org/10.4103%2F0974-8520.100303
  • 13
    Tripathi AS, Mazumder PM, Chandewar AV. Evaluation of drug interaction of glimepiride with phosphodiesterase inhibitors type V in diabetic nephropathy. Exp Clin Endocrinol Diabetes. 2014;122(10):597-601. https://doi.org/10.1055/s-0034-1382034
    » https://doi.org/10.1055/s-0034-1382034
  • 14
    Tripathi AS, Mazumder PM, Chandewar AV. Sildenafil, a phosphodiesterase type 5 inhibitor, attenuates diabetic nephropathy in STZ-induced diabetic rats. J Basic Clin Physiol Pharmacol. 2016;27(1):57-62. https://doi.org/10.1515/jbcpp-2015-0035
    » https://doi.org/10.1515/jbcpp-2015-0035
  • 15
    Knowler WC, Barrett-Connor E, Fowler SE, Hamman RF, Lachin JM, Walker EA, Nathan DM; Diabetes Prevention Program Research Group. Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. N Engl J Med. 2002;346(6):393-403. https://doi.org/10.1056/nejmoa012512
    » https://doi.org/10.1056/nejmoa012512
  • 16
    Schwartz SS, Kohl BA. Glycemic control and weight reduction without causing hypoglycemia: the case for continued safe aggressive care of patients with type 2 diabetes mellitus and avoidance of therapeutic inertia. Mayo Clin Proc. 2010;85(12 Suppl.):S15-26. https://doi.org/10.4065/mcp.2010.0468
    » https://doi.org/10.4065/mcp.2010.0468
  • 17
    Dejenie TA, Abebe EC, Mengstie MA, Seid MA, Gebeyehu NA, Adella GA, Kassie GA, Gebrekidan AY, Gesese MM, Tegegne KD, Anley DT, Feleke SF, Zemene MA, Dessie AM, Moges N, Kebede YS, Bantie B, Adugna DG. Dyslipidemia and serum cystatin C levels as biomarker of diabetic nephropathy in patients with type 2 diabetes mellitus. Front Endocrinol (Lausanne). 2023;14:1124367. https://doi.org/10.3389/fendo.2023.1124367
    » https://doi.org/10.3389/fendo.2023.1124367
  • 18
    Lopez-Giacoman S, Madero M. Biomarkers in chronic kidney disease, from kidney function to kidney damage. World J Nephrol. 2015;4(1):57-73. https://doi.org/10.5527/wjn.v4.i1.57
    » https://doi.org/10.5527/wjn.v4.i1.57
  • 19
    Vaziri ND. Disorders of lipid metabolism in nephrotic syndrome: mechanisms and consequences. Kidney Int. 2016;90(1):41-52. https://doi.org/10.1016/j.kint.2016.02.026
    » https://doi.org/10.1016/j.kint.2016.02.026
  • 20
    Su LJ, Zhang JH, Gomez H, Murugan R, Hong X, Xu D, Jiang F, Peng ZY. Reactive Oxygen Species-Induced Lipid Peroxidation in Apoptosis, Autophagy, and Ferroptosis. Oxid Med Cell Longev. 2019;2019:5080843. https://doi.org/10.1155/2019/5080843
    » https://doi.org/10.1155/2019/5080843
  • 21
    Nita M, Grzybowski A. The Role of the Reactive Oxygen Species and Oxidative Stress in the Pathomechanism of the Age-Related Ocular Diseases and Other Pathologies of the Anterior and Posterior Eye Segments in Adults. Oxid Med Cell Longev. 2016;2016:3164734. https://doi.org/10.1155/2016/3164734
    » https://doi.org/10.1155/2016/3164734
  • 22
    Imig JD, Ryan MJ. Immune and inflammatory role in renal disease. Compr Physiol. 2013;3(2):957-76. https://doi.org/10.1002/cphy.c120028
    » https://doi.org/10.1002/cphy.c120028
  • 23
    Cantero-Navarro E, Rayego-Mateos S, Orejudo M, Tejedor-Santamaria L, Tejera-Muñoz A, Sanz AB, Marquez-Exposito L, Marchant V, Santos-Sanchez L, Egido J, Ortiz A, Bellon T, Rodrigues-Diez RR, Ruiz-Ortega M. Role of Macrophages and Related Cytokines in Kidney Disease. Front Med (Lausanne). 2021;8:688060. https://doi.org/10.3389%2Ffmed.2021.688060
    » https://doi.org/10.3389%2Ffmed.2021.688060

Edited by

Section editor: Maria de Lourdes Biondo-Simões https://orcid.org/0000-0001-7056-8142

Publication Dates

  • Publication in this collection
    05 Aug 2024
  • Date of issue
    2024

History

  • Received
    20 Oct 2023
  • Accepted
    08 June 2024
Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia https://actacirbras.com.br/ - São Paulo - SP - Brazil
E-mail: actacirbras@gmail.com