{"id":53751,"date":"2023-12-31T11:22:24","date_gmt":"2023-12-31T11:22:24","guid":{"rendered":"https:\/\/biomedpharmajournal.org\/?p=53751"},"modified":"2024-01-05T06:21:33","modified_gmt":"2024-01-05T06:21:33","slug":"prophylactic-effects-of-coriander-aqueous-extract-on-carbendazim-induced-renal-toxicity-in-male-rats","status":"publish","type":"post","link":"https:\/\/biomedpharmajournal.org\/staging\/vol16no4\/prophylactic-effects-of-coriander-aqueous-extract-on-carbendazim-induced-renal-toxicity-in-male-rats\/","title":{"rendered":"Prophylactic Effects of Coriander Aqueous Extract on Carbendazim -Induced Renal Toxicity in Male Rats"},"content":{"rendered":"\n

Introduction<\/strong><\/p>\n\n\n\n

One of the most prevalent environmental contaminants, carbendazim (Carb) is a systemic benzimidazole fungicide. It is detrimental to both human and animal health and is essential for reducing plant diseases.1,2<\/sup> Carb is a “Toxic Substance” according to the World Health Organisation (WHO)3<\/sup>, and long-term exposure to carbs has been linked to a lower rate of human survival.4<\/sup> In order to interrupt the production of microtubules and meiotic cell division, the fungicidal activity of carbendazim targets tubulin.2,5<\/sup> Chronic low dosage administration of carbs may induce oxidative stress, which can lead to reproductive and endocrine damage.6,7<\/sup> Although previous research has shown that carbohydrates can be toxic due to the production of reactive oxygen species (ROS), there have been few attempts to investigate the role of antioxidants in reducing ROS-induced oxidative stress.7-9<\/sup><\/p>\n\n\n\n

A\nvariety of diseases can be treated using chemical compounds that are created by\nmedicinal plants.10-13<\/sup> <\/sup> Herbal medicines have special qualities\ncompared to modern pharmaceutical therapy, which is based on the production of\nseveral active molecules from the combination of unprocessed medicinal\ncomponents, each of which has its own pharmacological effects. 14,15<\/sup><\/p>\n\n\n\n

The\ndried seeds of coriander (Coriandrum sativum), a Mediterranean native also\nknown as Chinese parsley, have been utilised for food and fragrance purposes\nfor almost 7000 years in the Middle East.16<\/sup><\/a> In some\ntraditional spice mixtures, especially those used in “Indian Curry,”\na significant number of coriander seeds are utilised. There is no liquid\nessential oil mixture in substitute of this spice mixture. Coriander seeds are frequently used to season curries, puddings, breads,\nsausages, liqueurs, cakes, and spicy sauces.17,18<\/sup> The coriander plant has been demonstrated to have a significant\nrole in the etiology of several illnesses thanks to the discovery of certain\npolyphenolics and antioxidant components contained in it.19<\/sup> Its antioxidant, antibacterial, antifungal, and digestive\nqualities make it useful in medicine.18,<\/sup>20<\/sup><\/p>\n\n\n\n

According to pharmacological\nresearch conducted on animals, coriander exhibits anti-diabetic, anti-cancer,\nand hypolipidemic properties.17,21<\/sup>\nAntioxidants from food may be helpful in the fight against tissue damage.\nTherefore, there is a global quest for effective antioxidants to treat liver and\nstomach illnesses.22,18<\/sup> Future usage\nof coriander seeds as a free radical scavenger to stop oxidative food\ndegradation is possible.20<\/sup> This study\nlooked at the renal toxicity of carbendazim (Carb) and the potential\ntherapeutic value of Coriandrum sativum seed extracts (CSE) in albino rats.<\/p>\n\n\n\n

Material and Methods<\/strong><\/p>\n\n\n\n

Carbendazim\n(Carb) <\/strong><\/p>\n\n\n\n

The carb was obtained from Pesticides & Chemicals Company in\nKafr Elzayat, Gharbia, It was freshly made with maize oil and given orally.<\/p>\n\n\n\n

Coriander <\/strong>seeds extracts (CSE) production<\/strong><\/p>\n\n\n\n

Coriander seeds (CS) were ground into a powder, steeped in boiling\nwater for 24 hours, extracted, and then kept at -30\u00b0C in the dark until usage18<\/sup>.<\/p>\n\n\n\n

Animals and <\/strong>Experimental groups<\/strong><\/strong><\/p>\n\n\n\n

The experiments were performed on 50 male\nalbino rats (Rattus norvigicus<\/em>) weighing (140 g \u00b1 10g). Rats were kept\nin the laboratory for one week before the experimental work and maintained on a\nstandard rodent diet and water was available ad libitum. The rats were randomly\nand equally divided into five groups (10 rats each).   <\/p>\n\n\n\n

Gp1: Control Gp served as a negative\ncontrol and were not given any treatments.<\/p>\n\n\n\n

Gp2: Coriandrum Gp (CSE) where rats treated orally (50 mg\/kg body weight)\nfor 3 days weekly for 8 weeks.<\/p>\n\n\n\n

Gp 3: carbendazim Gp (Carb) where rats\ntreated orally with Carb (100 mg\/kg body weight) for 3 days weekly for 8 weeks.23<\/sup><\/p>\n\n\n\n

Gp 4: Co treated CSE with Carb (CSE + Carb) for 8 weeks.<\/p>\n\n\n\n

Gp 5: Post treated Carb with CSE (Carb+CSE) where rats treated with Carb\nfor 8 weeks and then treated with CSE for another 8 weeks.<\/p>\n\n\n\n

Blood and serum samples<\/strong><\/p>\n\n\n\n

Rats were then slaughtered after being given sodium pentobarbital\nanesthesia at the conclusion of the research. Blood samples were drawn\naseptically via a venipuncture and placed in a dry, clean, and sterile tube\nwithout the use of any anticoagulants, allowing the blood to clot. Blood\nsamples were centrifuged for 5 minutes at 4000 rpm after being allowed to stand\nfor 20 minutes at 4 o<\/sup>C to allow for coagulation. The obtained serum\nwas stored at -18 \u00b0C until a blood parameter was determined.<\/p>\n\n\n\n

Assessment\nof serum kidney function and electrolytes    \n<\/strong><\/p>\n\n\n\n

Kidney\nfunctions as Urea, Creatinine were assayed using a commercial kit (BIOSYSTEMS\nfrom Barcelona, Spain).24<\/sup> Electrolytes estimation were surveyed to measure the levels of\npotassium, calcium, sodium, and phosphorous using marketable kits of Indian\nSensa-core electrolyte. 25<\/sup><\/p>\n\n\n\n

Biochemical assesses<\/strong><\/p>\n\n\n\n

Using a Potter Elvenhjem tissue homogenizer, each piece of kidney\ntissue was weighed and processed independently. The undiluted tissue homogenate\nwas then whirled in a cold centrifuge for fifteen minutes at a speed of 11.739\nrcf. The resultant supernatant was then used to various estimates. <\/p>\n\n\n\n

Enzymatic and non-enzymatic antioxidant\nassays<\/strong><\/strong><\/p>\n\n\n\n

Malondialdehyde (MDA) levels in kidney tissue homogenate via using Biodiagnostic kits, Egypt.2<\/sup> After treating kidney homogenates with 5.5\u2032-dithiobis(2-nitrobenzoic acid), GSH concentration was determined using the Tipple and Rogers method and expressed as mol GSH\/ mg protein.27<\/sup> Nitric oxide (NO) activities were estimated in kidney homogenate as its stable metabolites, nitrate and nitrite. Nitrate was first reduced by nitrate reductase to nitrite and then nitrite was determined spectrophotometrically.28<\/sup><\/p>\n\n\n\n

Histological\nprocessing<\/strong><\/strong><\/p>\n\n\n\n

After\nnecropsy, the kidney was quickly removed and immersed in a 10% neutral buffered\nformalin solution to preserve it for 24-48 hours. The specimens are dehydrated,\ncleared, and paraffin embedded. Serial sections that were 5 thick were cut into\nslices and stained with hematoxylin and eosin using a rotary microtome (Litz,\nWetzlar, Germany). 29<\/sup><\/p>\n\n\n\n

Proliferating cell nuclear antigen (PCNA)<\/strong><\/strong><\/p>\n\n\n\n

The detection\nof PCNA expression used the avidin-biotin complex method. Using Image J’s\ncolour thresholding for quantitation feature, the stained cells’ brown hue was restored.30<\/sup><\/p>\n\n\n\n

Statistical Assessment<\/strong><\/p>\n\n\n\n

Data were reported as the one-way ANOVA was\nused to examine the significance of difference. *and# significant difference\nfrom control and from EST group respectively. Values are expressed as means SE\nat p< 0.05.<\/p>\n\n\n\n

Results<\/strong><\/p>\n\n\n\n

Impacts of <\/strong>CSE<\/strong> on kidney functions and electrolytes<\/strong><\/p>\n\n\n\n

Table 1 exposed that; Carb induced a significant elevation in serum creatinine, urea, potassium, and significant depletion in the level of calcium and sodium ions, as compared control and CSE groups. Treatment of Carb with CSE as co-treatment group (CSE+Carb) or post treatment group (Carb+CSE) revealed a significant depletion in the level of creatinine, urea, potassium, and significant elevation in the level of calcium and sodium ions as compared to Carb group with best results for Carb+CSE. Serum phosphorus revealed no significant changes between different groups.<\/p>\n\n\n\n

Table 1: Modifications in the levels of kidney functions & electrolytes. <\/strong><\/p>\n\n\n\n\n\n\n\n\n\n\n\n
\n

Carb+CSE<\/strong><\/p>\n<\/td>\n

\n

CSE+Carb<\/strong><\/p>\n<\/td>\n

\n

Carb<\/strong><\/p>\n<\/td>\n

\n

CSE<\/strong><\/p>\n<\/td>\n

\n

Control<\/strong><\/p>\n<\/td>\n

\n

 <\/strong><\/p>\n<\/td>\n<\/tr>\n

\n

38.30# <\/sup> \u00b1 2.37<\/p>\n<\/td>\n

\n

47.9*#<\/sup> \u00b1 3.60<\/p>\n<\/td>\n

\n

72.5* \u00b1 4.19<\/p>\n<\/td>\n

\n

35.4# <\/sup> \u00b1 2.23<\/p>\n<\/td>\n

\n

35.7# <\/sup>\u00b1 2.81<\/p>\n<\/td>\n

\n

Creatinine (mg\/dl)<\/p>\n<\/td>\n<\/tr>\n

\n

0.92# <\/sup> \u00b1 0.04<\/p>\n<\/td>\n

\n

1.14*#<\/sup> \u00b1 0.04<\/p>\n<\/td>\n

\n

1.54* \u00b1 0.08<\/p>\n<\/td>\n

\n

0.81# <\/sup> \u00b1 0.06<\/p>\n<\/td>\n

\n

0.85# <\/sup> \u00b1 0.02<\/p>\n<\/td>\n

\n

Urea (mg\/dl)<\/p>\n<\/td>\n<\/tr>\n

\n

131.9*# <\/sup> \u00b1 6.20<\/p>\n<\/td>\n

\n

127.6*#<\/sup> \u00b1 8.53<\/p>\n<\/td>\n

\n

124.9* \u00b1 6.55<\/p>\n<\/td>\n

\n

136.6# <\/sup> \u00b1 7.32<\/p>\n<\/td>\n

\n

134.1# <\/sup> \u00b1 5.39<\/p>\n<\/td>\n

\n

Na+ (mEq\/L)<\/p>\n<\/td>\n<\/tr>\n

\n

3.65# <\/sup> \u00b1 0.16<\/p>\n<\/td>\n

\n

3.97*#<\/sup> \u00b1 0.23<\/p>\n<\/td>\n

\n

4.24* \u00b1 0.19<\/p>\n<\/td>\n

\n

3.58# <\/sup> \u00b1 0.13<\/p>\n<\/td>\n

\n

3.61# <\/sup> \u00b1 0.17<\/p>\n<\/td>\n

\n

K+ (mEq\/L)<\/p>\n<\/td>\n<\/tr>\n

\n

4.36 \u00b1 0.19<\/p>\n<\/td>\n

\n

4.37 \u00b1 0.35<\/p>\n<\/td>\n

\n

4.38 \u00b1 0.11<\/p>\n<\/td>\n

\n

4.38 \u00b1 0.12<\/p>\n<\/td>\n

\n

4.37 \u00b1 0.65<\/p>\n<\/td>\n

\n

Ph (mEq\/L)<\/p>\n<\/td>\n<\/tr>\n

\n

9.41# <\/sup> \u00b1 0.37<\/p>\n<\/td>\n

\n

9.04*#<\/sup> \u00b1 0.41<\/p>\n<\/td>\n

\n

8.80* \u00b1 0.24<\/p>\n<\/td>\n

\n

9.58# <\/sup> \u00b1 0.30<\/p>\n<\/td>\n

\n

9.60# <\/sup> \u00b1 0.28<\/p>\n<\/td>\n

\n

Ca++ (mEq\/L)<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

The significance of modification was analyzed by one \u2013 way ANOVA. Values are expressed as means \u00b1 SE. *and #<\/sup> significant deviation from the Carb group and the control, respectively at p< 0.01.<\/p>\n\n\n

Oxidative stress and antioxidant parameters in kidney homogenates <\/strong><\/p>\n\n\n\n

Table 2 demonstrated a statistically significant elevation in the level of MDA and NO while a significant depletion in GSH in kidney homogenates in the Carb group compared to the control and CSE groups. In distinction; when Carb\nwere treated with CSE (CSE+Carb or as Carb+CSE), kidney\nhomogenates showed a significant elevation in GSH and a\nsignificant depletion\nin MDA and NO with best results for Carb+CSE.<\/p>\n\n\n\n

Table 2: Activities of malondialdehyde (MDA; nmol\/g protein), glutathione (GSH; \u00b5mol\/g tissue), and nitric oxide (NO; \u00b5mol\\L) in kidney tissue of male treated rats.<\/strong><\/p>\n\n\n\n\n\n\n\n\n
\n

Carb+CSE<\/strong><\/p>\n<\/td>\n

\n

CSE+Carb<\/strong><\/p>\n<\/td>\n

\n

Carb<\/strong><\/p>\n<\/td>\n

\n

CSE<\/strong><\/p>\n<\/td>\n

\n

Control<\/strong><\/p>\n<\/td>\n

\n

 <\/p>\n<\/td>\n<\/tr>\n

\n

8.83#<\/sup> \u00b1 0.55<\/p>\n<\/td>\n

\n

13.44*#<\/sup> \u00b1 0.65<\/p>\n<\/td>\n

\n

20.05* \u00b1 1.19<\/p>\n<\/td>\n

\n

4.96#<\/sup> \u00b1 0.32<\/p>\n<\/td>\n

\n

5.81#<\/sup> \u00b1 0.26<\/p>\n<\/td>\n

\n

MDA<\/p>\n<\/td>\n<\/tr>\n

\n

0.473#<\/sup> \u00b1 0.046<\/p>\n<\/td>\n

\n

0.953*#<\/sup> \u00b1 0.023<\/p>\n<\/td>\n

\n

2.151* \u00b1 0.058<\/p>\n<\/td>\n

\n

0.375#<\/sup> \u00b1 0.061<\/p>\n<\/td>\n

\n

0.414#<\/sup> \u00b1 0.029<\/p>\n<\/td>\n

\n

NO<\/p>\n<\/td>\n<\/tr>\n

\n

1.698#<\/sup> \u00b1 0.033<\/p>\n<\/td>\n

\n

1.271*#<\/sup> \u00b1 0.108<\/p>\n<\/td>\n

\n

1.169* \u00b1 0.124<\/p>\n<\/td>\n

\n

1.769#<\/sup> \u00b1 0.0177<\/p>\n<\/td>\n

\n

1.853#<\/sup> \u00b1 0.029<\/p>\n<\/td>\n

\n

GSH<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

The significance of modification was analyzed by one \u2013 way ANOVA. Values are expressed as means \u00b1 SE. *and #<\/sup> significant deviation from the Carb group and the control, respectively at p< 0.01.<\/p>\n\n\n

Histological observations<\/strong><\/p>\n\n\n\n

Impact of <\/strong>CSE<\/strong> in kidney\nstructure<\/strong><\/p>\n\n\n\n

Glomruli and tubules in the cortical and medullary parts of the kidneys in the control and CSE groups had normal histological features (Figure 1A&B). Contrarily, the kidney sections of the rats treated with Carb revealed marked tubular cell and glomerular atrophy, vaculation, and distinct necrotic tubular cells (Figure 1C&D). As opposed to that; kidney sections in CSE+Carb revealed moderate necrosis, atrophy of the renal corpuscles and mild inflammatory cells (Figure 1E). Kidney sections in Carb+CSE showed significant improvement in the glomruli with mild renal tubules atrophy (Figure 1F).<\/p>\n\n\n\n

PCNA expression changes in kidney<\/strong><\/p>\n\n\n\n

Mild reactions in nuclei were presented after PCNA expressions in kidney sections in control and CSE groups (Figure 2A&B). while; a strong reaction was presented in Carb group (Figure 2C&D). As opposed to that; moderate reaction for PCNA was presented in CSE+Carb while mild reaction was detected in Carb+CSE (Figure 2E&F). <\/p>\n\n\n\n\n\n
\"\"<\/td>\n\n

Figure 1: <\/strong>Hematoxylin and Eosin-stained photomicrographs of kidney sections from the various experimental groups.<\/strong><\/p>\n

<\/p>\n

Click here to view Figure<\/a><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n\n\n\n
\"\"<\/td>\n\n

Figure 2: <\/strong>Photomicrographs of kidney sections stained with PCNA in different groups.<\/strong><\/p>\n

<\/p>\n

Click here to view Figure<\/a><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n\n\n

Discussion<\/strong><\/p>\n\n\n\n

Various health risks are directly caused by environmental pollutants on living things. Pesticides are mostly to blame for environmental contamination. A pesticide is a chemical or biological agent used to prevent, repel, or eliminate pests that might harm or impair the development and well-being of living things, including both plants and animals. The broad spectrum benzimidazole carbamate fungicide carbendazim (carb), which has systemic action, is used to treat a variety of fungal diseases that affect field crops, fruits, ornamentals, and vegetables. In developing and adult animals, exposure to pesticides causes cytotoxicity, genotoxicity, and embryotoxicity alterations.31<\/sup><\/a> Despite their significant usage and global dissemination, the function of pesticides in the development of illnesses in people is still debatable. Therefore the current study aimed to study the impact of CSE against Carb induced toxicity, oxidative stress and tissue injury in male rat kidney. Creatinine and urea are nitrogenous metabolic byproducts. The main byproduct of dietary protein and tissue protein turnover is urea. Muscle creatine catabolism results in creatinine. Both are bodily water-distributed molecules that are quite tiny. Current results revealed that; Carb induced elevation in urea, creatinine, potassium levels and depletion in sodium, calcium as compared to control and CSE while the treatments with CSE in both cases of co- or\/and post treatments improved this modulation. Elevation of serum urea observed in the present study in response to pesticides exposure may be explained by impairment in its synthesis as a result of impaired hepatic function, or for the disturbance in protein metabolism as found in the present results or the  decrease in the filtration rate of the kidney. Since urea and creatinine are indicators of renal function, elevations in these levels may be explained by the synergistic effects of carbendazim toxicity.32<\/sup> which would reduce the kidneys’ ability to eliminate these metabolic wastes. Current results agree with 33,<\/sup> 34<\/sup> who find that Carb induced renal toxicity. Current results agree with 35<\/sup> who reported that there was an increase in blood urea due to Carb. Increase in urea content is indicative of an increase in tissue ammonia generation. It is therefore possible that elevation of urea and creatinine levels is the consequence of metabolic changes in rat cells brought about by these pesticides. <\/p>\n\n\n\n

Current results agree with 31<\/sup> who studied the protective effect of CSE on hepato-renal toxicity, also agree with 36<\/sup> who reported that coriander seeds improved the renal toxicity by carbon tetrachloride. In addition to current results agree with 37<\/sup> who reported that coriander seeds extract have the ability to improve the hepato-renal toxicity induced by sodium arsenite. Also, current results agree with 38<\/sup> who reported that; CSE have the ability to improve the renal oxidative stress induced by lead, also; agree with 16<\/sup> who reported that Coriandrum sativum extract contributes to resistance to oxidative stress via decreases in heavy metal concentrations in the kidney. <\/p>\n\n\n\n

Environmental pollution-induced oxidative stress increases the expression of ROS, which in turn weakens the antioxidant defence system39,40<\/sup>; According to 41-43<\/sup>, it has been discovered that many pesticides cause oxidative stress, which produces free radicals and an alternative antioxidant or oxygen free radical scavenging enzyme system. Malonyldialdehyde (MDA), a marker of tissue membrane deterioration that is produced when carbs are consumed, was found to be elevated in the kidneys of the present study’s participants.44<\/sup> This rise in MDA concentration may also reflect membrane instability and point to oxidative stress. Additionally, our findings indicated a GSH depletion in the kidneys, and CSE therapy modifies these findings.  These GSH and NO measurements in the kidney point to an imbalance in the animal’s antioxidant system, which in turn causes increased membrane peroxidation in the organs. Current findings support the claims made 34.44<\/sup> who find that carbs cause renal oxidative stress in rats by raising ROS levels.  Current findings support 45,46<\/sup> who found that CSE reduced renal tissue damage and oxidative stress brought on by lead nitrate.<\/p>\n\n\n\n

Conclusion<\/strong><\/p>\n\n\n\n

Carbamate fungicide (carbendazim; Carb) induced liver toxicity\nwhere it changes liver structure and functions. Treatments of carbendazim\nwith  Coriandrum sativum seeds extract (Carb+CSE)\nmodulates and improved these parameters with best results for post\ntreatments than co-treatments.<\/p>\n\n\n\n

Conflict of Interest<\/strong><\/p>\n\n\n\n

The authors declare no competing interests.<\/p>\n\n\n\n

Funding Sources<\/p>\n\n\n\n

References<\/strong><\/p>\n\n\n\n

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