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Biochemical and Histopathological Effects of Repeated Low Oral Doses of Malathion, Metalaxyl and Cymoxanil on Different Tissues of Rats

PJZ_55_1_11-21

Biochemical and Histopathological Effects of Repeated Low Oral Doses of Malathion, Metalaxyl and Cymoxanil on Different Tissues of Rats

Ahmed H. Massoud1, Mohamed S. Ahmed2, Moustafa Saad-Allah1,

Aly S. Derbalah1, Ashraf Albrakati3* and Ehab Kotb Elmahallawy4*

1Pesticides Chemistry and Toxicology Department, Faculty of Agriculture, Kafrelshiekh University 33516 Egypt

2Department of Pathology, Faculty of Veterinary Medicine, Kafrelsheikh University, Kafrelsheikh 33516, Egypt

3Department of Human Anatomy, College of Medicine, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia

4Department of Zoonoses, Faculty of Veterinary Medicine, Sohag University, Sohag 82524, Egypt

ABSTRACT

Most of the pesticides can be used with little risk if label directions were followed, while some are extremely toxic and require special precautions. This study aimed to determine the patho-biochemical toxicity of short-term exposure to repeated low oral doses of malathion, metalaxyl and cymoxanil pesticides on male rats. Results of the present study demonstrated that low doses of malathion, metalaxyl and cymoxanil pesticides was asymptomatic and mostly showed insignificant histopathological changes in treated rats. The observed values of biochemical enzymes with these low-doses were near to the control ones, whereas medium and high doses treated rats exhibited adverse signs and symptoms of toxicity. The results also depicted that cymoxanil was the most toxic of the tested pesticides, followed by Malathion and metalaxyl. The obtained histological lesions were correlated with the increased level of biochemical enzymes in target organs. Additionally, hepatotoxicity and nephrotoxicity were obvious in rats treated with cymoxanil, meanwhile, neuronal and pulmonary changes were nearly the same in all doses of the used pesticides. Taken together, our study recommends examining pesticides for their possible adverse effects on animals and humans in case of repeated use, even in small doses, before their application to agricultural fields.


Article Information

Received 18 May 2021

Revised 25 January 2022

Accepted 01 February 2022

Available online 02 June 2022

(early access)

Published 14 October 2022

Authors’ Contribution

AHM and MS Ahmed presented the concept and methodology and perfromed formal analysis. MS Allah analysed the data and provided statistical guidance. ASD, AA and EKE helped in software, data curation and resources. MS Allah, ASD, AA, EKE AHM and MS Ahmed wrote, reviewed and edited the manuscript.

Key words

Pesticides, Malathion, Metalaxyl, Cymoxanil, Transaminases, ACHE, Creatinine

DOI: https://dx.doi.org/10.17582/journal.pjz/20210518100521

* Corresponding author: a.albrakati@tu.edu.sa,

eehaa@unileon.es

0030-9923/2023/0001-11 $ 9.00/0

Copyright 2023 by the authors. Licensee Zoological Society of Pakistan.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).



INTRODUCTION

Pesticides are natural or synthetic compounds used to control plant diseases and pests and they can be classified according their application into herbicides, insecticides and fungicides (Fantke and Juraske, 2013; Sun et al., 2019). Pesticides can cause intoxication through skin contact, ingestion, or inhalation and their risk is to produce harmful effects and even fatality to human (Zuskin et al., 2008). However, great efforts have been spent to produce pesticides of lower risk to human and animals and of low environmental hazards than the currently used pesticides, it seems difficult to get rid of all pesticides with toxic effects due to its importance in some specific purposes and due to inability to provide safe substitutions (Han et al., 2017). Some pesticides are dangerous after single dose and others can be dangerous after repeated doses (Zuskin et al., 2008; Aardema et al., 2008). Nowadays the emerging problem is the hazards of long-term and low-dose effects of pesticides on human and animals due to its excessive use (Liu et al., 2014). Among others, malathion is the most commonly used pesticide in a vast manner throughout the world to control pests of crops, livestock, ornamentals, stored grain, buildings, households and gardens (Hazarika et al., 2003). Metalaxyl is a systemic, benzenoid fungicide used in mixtures as a foliar spray for wide range of fungal pathogens of fruits and crops by inhibition of mycelial growth and spore formation of these fungi (Urech et al., 1977). In addition, cymoxanil is abroad spectrum and systemic fungicide has a protective and curative effects against a wide range of fungal diseases in crops (Fazilat et al., 2017). It is noteworthy to state that malathion, metalaxyl and cymoxanil can cause a biochemical and histological alterations on humans and animals (Okdah, 2005). The best ways to determine and evaluate the toxicity of different organophosporus compounds (OP) are the assessment of biochemical parameters alterations and histopathological changes in tissues and organs (Ghanem et al., 2006). It is well known that, the assessment of blood enzyme activity is more sensitive measure of toxicity and takes shorter time than histopathological examination; meanwhile, the tissue alterations are considered a confirmatory and supporting diagnostic tool (Huang et al., 2019). Given the above information, this study was carried out to study the patho-biochemical toxicity of short-term exposure to repeated low oral doses of malathion, metalaxyl and cymoxanil in male rats.

MATERIALS AND METHODS

Ethical statement

The ethical approval was performed as described by the ethical standards of Veterinary Medicine, Kafrelsheikh University, Egypt, and which complies with all relevant Egyptian legislations.

Chemical

Malathion 99% was applied (Prochem Co. Ltd., Warsaw, Poland), metalaxyl is a colorless, odorless crystal, was provided by Ciba-Geigy Corporation and Cymoxanil tech, off white powder, was provided by Saturn Agrochemical Inc, Shenzhen, Guangdong, China.

Animals

Forty adult male SD rats weighing 100–120 g were obtained from faculty of medicine, Tanta University and acclimatized for one week prior to the experiment. All Rats were housed in polypropylene cages under standard conditions of 12 h light/dark cycle; at 22 ± 2◦ temperature and 30–70% relative humidity. Rats were well ventilated, standard rat feed and water were provided ad libitum (Korsrud et al., 1972).

Animal treatment

Rats were divided into 9 treated groups and one control group (4 rats in each group). Each 3 treated groups of rats received a diet containing low dose (0.5mg/kg/day), medium dose (1mg/kg/day), and high dose (2mg/kg/day) of Malathion, metalaxyl and cymoxanil respectively dissolved in almond oil for successive 21 days. Control group rats were fed normal diet containing equal amount of almond oil. Clinical signs and mortality of the rats were observed once per hour for 6 h after dosing and once daily thereafter. The body weights were measured once a week during the whole observation period. All animal studies were approved by our Institutional Animal Ethics Committee.

Histopathological examination

At the end of the study, all the animals were anesthetized and sacrificed. Postmortem examination was performed and lesions were recorded. Specimens from all organs especially liver, brain, kidneys, lungs and testis were taken and kept in 10% neutral buffered formalin for histopathological examination. Specimens were then dehydrated in ascending grades of alcohols, cleared in xylene, embedded in paraffin wax, sectioned at 4µm, stained with hematoxylin and eosin (HE), and examined by light microscope (Bancroft and Gamble, 2008).

Biochemical determinations

Blood samples were taken shortly before sacrifice, under anesthesia by cardiac puncture, in vials without anticoagulant. Serum was obtained by centrifuging the blood at 3000 rpm for 5 min and kept at −20 oC until be used. Liver, brain and kidneys of both treated and control rats were quickly separated on ice cold 0.8 M sucrose containing 1mM phenyl methane sulphonyl fluoride (PMSF) using Miccra D-1-high speed tissue homogenizer to make 10% homogenate (w/v). The homogenate was then centrifuged at 10 000× g for 10 min at 4 oC. The supernatant was used as enzyme source. Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), alkaline phosphatase (ALP) and Creatinine were determined from the serum and supernatant of the homogenate of liver and kidneys as mentioned elsewhere (Reitman and Frankel, 1957; Barham and Trinder, 1972). The activity of Acetylcholinesterase (AChE) was determined according to the method described (Ellman et al., 1961; Rahman et al., 2000).

Statistical analysis

The statistical analysis of the treatment was performed by one-way ANOVA using SPSS statistical software package for windows version 11.0. Duncan’s multiple-range test was used to find out the group effects. P≤0.05 was set as limit of significance.

RESULTS

Clinical signs and postmortem examination

There was no significant difference in daily activity, clinical observation, body weight and water and food consumption between the treated groups with (low, medium and high) of Malathion, low and medium dose of both metalaxyl and cymoxanil and the respective control groups. However, shortly before the end of the experiment, rats treated with high dose of metalaxyl exhibited transient hypo-activity and rats treated with high dose of cymoxanil showed lethargy, dullness, incoordination, reduced body weight and feed intake, but the loss of weight was not significant. No deaths occurred throughout the study period in the treated groups. Furthermore, no macroscopic visible changes were found in organs of treated rats during postmortem examination.

 

Histopathological changes in the liver

Rats treated with low dose of Malathion and metalaxyl showed slight congestion and dilatation of the hepatic sinusoids which were similar to that found in the control rats (Fig. 1A, B). Meanwhile, those rats treated with low dose of cymoxanil showed slight sinusoidal cell activation with pregranuloma formation (Fig. 1C). Liver of rats treated with medium dose of malathion showed marked cytosolic hydrops with vacuolated cytoplasm of the hepatocytes (Fig. 1D), while liver of rats treated with medium dose of metalaxyl showed moderate inflammatory reaction in the form of focal collection of mononuclear cells within the hepatic parenchyma and in the portal triad (Fig. 1E). Moreover, some areas of the hepatic lobules appeared with slight fatty changes and apoptosis, but rats treated with medium dose of cymoxanil showed focal hepatocytic necrosis with moderate infiltration of mononuclear cells and haemorrhages in the hepatic parenchyma (Fig. 1F). On the other hand, rats treated with high doses of malathion showed granuloma like reaction with focal collection of kupffer cells and focal hepatocellular coagulative necrosis (Fig. 1G); meanwhile liver of rats treated with high dose of metalaxyl and cymoxanil showed extensive piecemeal necrosis and the hepatocytes were lost their normal architecture with infiltration of mononuclear cells in the margin and within the necrosed areas (Fig. 1H, I).

The histopathological changes in the brain

There were no obvious changes recorded in the brain of rats treated with malathion and metalaxyl at low dose (Fig. 2A, B), but rats treated with low dose of cymoxanil showed slight lymphocytic perivascular infiltration (perivascular cuff) (Fig. 2C). Rats treated with medium dose of malathion showed neuronal cell degeneration and few hemorrhagic areas in the brain tissue (Fig. 2D), while rats received medium dose of metalaxyl exhibited slight spongiosis (Fig. 2E) and slight spongiosis and scattered focal collections of glial cells forming Babe’s bodies was observed in rats treated with medium dose of cymoxanil (Fig. 2F). Brain lesions became more pronounced in the rats treated with high dose of all three pesticides, represented by moderate perivascular edema, cerebral hemorrhages and features of focal early malacia in the cerebral cortex in malathion treated rats (Fig. 2G). Obvious cerebral spongiosis and gliosis was reported in rats treated with metalaxyl (Fig. 2H) and cerebral liquifactive necrosis (malacia) with newly formed blood capillaries in rats treated with cymoxanil (Fig. 2I).

The histopathological changes in the kidneys

Rats treated with malathion and metalaxyl in low dose did not show any changes which is similar to that of the control rats (Fig. 3A, B), meanwhile, those treated with low dose of cymoxanil showed slight interstitial nephritis with intertubular infiltration of mononuclear cells (Fig. 3C). Kidneys of rats treated with medium dose of malathion and metalaxyl showed slight vacuolar degenerative changes in the renal tubules lining epithelium (Fig. 3D, E), but rats treated with medium dose of cymoxanil exhibited slight interstitial nephritis with intertubular infiltration of mononuclear cells (Fig. 3F). More severe changes were observed in the kidneys of all groups, marked interstitial nephritis and plugging of renal tubules lumens with proteinaceous casts in malathion treated rats (Fig. 3G), cloudy swelling degeneration was observed in the epithelial lining of the renal tubules forming star shape like lumens in metalaxyl treated rats (Fig. 3H). Meanwhile, rats treated with high dose of cymoxanil showed marked renal changes in the form of severe interstitial nephritis and thickening and sclerosis of the Bowman’s capsule and the surrounding renal tubules (Fig. 3I).

 

The histopathological changes in the lungs

There were no microscopic changes observed in the lungs of rats treated with malathion and metalaxyl at low dose level and lungs showing the same architecture which is similar to that of control ones (Fig. 4A, B), but rats treated with low dose of cymoxanil showed slight perivascular mononuclear cells infiltration (Fig. 4C). On the other hands, rats treated with malathion medium dose lungs showed interstitial pneumonia with marked thickening in the interalveolar septa (Fig. 4D), while those treated with medium dose of metalaxyl and cymoxanil exhibited slight interstitial pneumonia (Fig. 4E) and moderate interstitial pneumonia (Fig. 4F), respectively. In addition, there were marked bronchopneumonia with massive peribronchial infiltration of mononuclear cells (Fig. 4G) in rats treated with high dose of the three chemicals. Furthermore, light interstitial pneumonia (Fig. 4H) was observed in rats treated with high dose of malathion, while those treated with high dose of metalaxyl and cymoxanil exhibited marked interstitial pneumonia with pneumocyte type II hyperplasia (Fig. 4I).

 

The histopathological changes in the testis

No pathological changes were detected in seminiferous tubules and interstitial tissue in rats treated with low dose of malathion, cymoxanil and to low, medium, high dose of metalaxyl. The seminiferous tubules appeared uniform in size and shape and they were lined by arranged rows of spermatogenic cells in different stages of maturation. Spermatogenic cells and sertoli cells in the seminiferous tubules were observed in normal structure. Leydig cells and blood vessels were found in the interstitial connective tissue between the tubules (Fig. 5A). Rats treated with medium dose of malathion and cymoxanil showed decrease in the number of spermatogenic cells in the seminiferous tubules (Fig. 5B) and interstitial edema (Fig. 5C), respectively. Meanwhile, rats treated with high dose of malathion revealed marked vacuolation in the cytoplasm of sertoli cells (Fig. 5D) and those rats treated with high dose of cymoxanil showed massive necrosis in the lining epithelium of seminiferous tubules with marked interstitial oedema (Fig. 5E).

 

 

Effects on liver function

The obtained data showed that treated rats with malathion at low and medium dose and metalaxyl at low dose group did not show any changes in the AST, ALT and ALP activity which is similar to that of control ones. The activity was slightly increased in rat groups treated with high dose of malathion, medium dose of metalaxyl and low dose of cymoxanil. Rats treated with high dose of metalaxyl and medium dose of cymoxanil showed higher activity of liver enzymes and the activity was markedly increased in those rats treated with high dose of cymoxanil (Table I).

Effect on brain function

Low dose of malathion and cymoxanil slightly decreased the ACHE activity but nearly the same like control rats. However, low dose of cymoxanil showed more decrease in ACHE activity. The three chemicals showed medium decrease in the activity at medium dose level, but higher doses of malathion and metalaxyl exhibited slightly decrease but cymoxanil showed sharp decrease in the activity of ACHE (Table I).

 

Table I. Biochemical changes in male rats treated with repeated low oral doses of malathion, metalaxyl and cymoxanil pesticides.

Parameter

Control

0.5 mg/kg/day

1 mg/kg/day

2 mg/kg/day

Mala-thion

Meta-laxyl

Cymo-xanil

Mala-thion

Meta-laxyl

Cymo-xanil

Mala-thion

Meta-laxyl

Cymo-xanil

AST (U/ml)

13.44± 0.59d

13.58± 1.15c

13.91± 0.98c

17.36± 0.92c

13.98± 1.39b

16.34± 0.92b

18.25± 1.60b

14.98± 0.89a

18.06± 1.15a

25.51± 1.46a

ALT (U/ml)

17.76± 0.46d

17.66± 1.52c

16.68± 1.39d

23.96± 1.76c

17.97± 1.01b

20.21± 0.99b

22.75± 1.98b

21.39± 1.82a

24.74± 1.61a

33.28± 1.02a

ALP (U/100ml)

2.79± 0.70d

2.89± 0.66b

3.16± 0.65b

4.15± 0.48c

3.16± 0.14a

3.16± 0.67b

4.54± 0.83b

3.17± 0.01a

4.51± 0.54a

5.36± 0.50a

ACHE

0.95× 10-4±0.05a

0.87× 10-4±0.01b

0.72× 10-4±0.06b

0.88× 10-4±0.01a

0.75× 10-4±0.01a

0.75× 10-4±0.03b

0.75× 10-4±0.04b

0.67× 10-4±0.02a

0.65× 10-4±0.04c

0.37× 10-4±0.07c

Creatinine (Mg/di)

0.32± 0.021c

0.34± 0.020b

0.27± 0.006b

0.77± 0.009b

0.35± 0.013b

0.27± 0.025b

0.78± 0.016b

0.45± 0.019a

0.35± 0.021a

0.95± 0.016a

 

All data was expressed as mean ± S.D (number of replicates=3). Means within the same column (in each parameter) carrying different superscripts (a, b, c, d) is significantly different (p <0.05).

 

Effects on kidneys function

Creatinine level was similar to that of control in rats treated with low dose malathion and low and medium dose of metalaxyl. On the other hand, the level of creatinine increased in rats treated with low dose of cymoxanil, medium dose of malathion and high dose of metalaxyl. The creatinine level was severely increased in rats treated with high dose of malathion and cymoxanil (Table I).

DISCUSSION

Investigation the adverse effects of chemical pollutants and pesticides are considered one of major concern for human health. The present study provides interesting data in relation to the patho-biochemical toxic effects of the repeated low oral doses of Malathion, Metalaxyl and Cymoxanil Pesticides on male rats. In the present study, no treatment-related differences or clinical signs were found between treated rats with malathion in all doses, metalaxyl and cymoxanil at low and medium doses and controls during the study period. It seems that the used doses gave an indication about the no observed effect level (NOEL) as the rats were asymptomatic. However, appearance of clinical signs of toxicity at the end of the experiment in the high dose treated rats with metalaxyl and cymoxanil is an interesting finding that reflects the changes in enzyme activities occurred after accumulation of large amount of the toxicants which resulted in stress condition of these chemicals on rats, which is in agreement with several previous studies (Rahman et al., 2000; Awal and Malik, 1992). No deaths occurred throughout the study period in the all treated rat groups and no treatment-related gross changes in organs were seen at necropsy.

In accordance with the histopathological changes, the present study revealed that liver appeared normal in lobulation and arrangement of hepatic cords in rats treated with low dose of malathion and metalaxyl. Inflammatory reaction in the liver parenchyma and portal triad, fatty changes and hepatic necrosis were observed in rats treated with high doses of the three studied chemicals, indicating dose dependent toxicity, which is correlated with the increased level of liver enzymes that rendered to subchronic liver damage. These results are in agreement with some previous reports (Sayim, 2007; Kim et al., 2008; Singh et al., 2013; Toś-Luty et al., 2003), who found that exposing male Wistar rats to a single dose of malathion, caused degenerative changes in the liver in the form of parenchymatous degeneration. In addition, a previous study noticed congestion of blood vessels, increased in number of Kupffer cells, cellular infiltration and hydropic degeneration in liver of male rats treated with metalaxyl (Okdah, 2005). We assumed that these lesions may arise from the toxic effect of the high doses of these chemicals, which disturbs the detoxification mechanisms of the liver and induces an inflammatory response comparable with the dose of the all three compounds dosed (Gokcimen et al., 2007; Lee et al., 2016; Yehia et al., 2007). It is well known that; liver is the primary organ concerned with detoxification in the body that acts through p450 mediated enzymatic catalysis. Clearly, it seems that cymoxanil, like several other pesticides, adversely affects the cytochrome P450 system or the mitochondrial membrane transport system of hepatocytes that induced liver damage and cell death in the treated rats with high dose of malathion, metalaxyl and cymoxanil. This led to inhibition of the p450 -mediated biocatalysis which is in agreement with some previous reports (Gokcimen et al., 2007; Guengerich and Avadhani, 2018; He et al., 2020). We suggest that the high dose of the used chemicals led to reduction in antioxidant enzymes activities resulted in oxidative damage of the liver tissue, particularly in rats treated with metalaxyl (Nakatani et al., 2000).

Brain is a highly susceptible organ for toxicity, because it contains relatively low levels of the anti-oxidative stress enzymes and in part because of its high myelin-associated contents, making it vulnerable to the propagation of peroxidative process (Savolainen, 1978). As depicted in our results, brain showed no histopathological changes in groups of rats treated with low dose of malathion and metalaxyl which is similar to brain of control group. Histopathological changes became more severe in other treated groups with medium and high dose of malathion and metalaxyl and in all groups treated with cymoxanil. The noticed changes indicated that the brain damage was nearly dose dependent in the rats treated with all the toxic materials. In the present study, the low dose exposed rats were mostly asymptomatic, but medium and high dose treated rats exhibited signs and symptoms of toxicity (Cheng et al., 2020). Many pesticides cause neurotoxicity and they kill insects by targeting their nervous system besides reported neurotoxic effect in mammals (Ahmed et al., 2020). It seems that the used pesticides interfere with chemical neurotransmission or ion channels, and cause reversible neurotoxic effects such as neuritis and gliosis, which is consistent with several previous reports (Eddleston et al., 2002; Gunnell et al., 2007). The noticed spongiosis could be attributed to the loss or damage of myelin sheath which is a substance encloses nerves and formed from fats and proteins that helps in transmitting signals along the nerves (Lotti and Johnson, 1978; Stacey et al., 2004).

To author’s knowledge, renal clearance of chemicals through glomerular filtration is time-dependent and it depends on their physiochemical properties. In this concern, particles of 7 nm or above usually cannot pass through the glomerular endothelial cells, and hence are not cleared (Iavicoli et al., 2016). In the present study, the effect of all used pesticides on the kidneys of all treated groups was dose dependent. Kidneys of rats treated with low dose did not show any microscopic abnormalities and medium dose treated rats exhibited slight microscopic changes. However, marked renal changes were recorded in rats treated with high dose of malathion, metalaxyl and cymoxanil, respectively. These induced histopathological changes were in consistence with that reported elswhere (Afshar et al., 2008; Mamun et al., 2015). We think that high doses of the used chemicals resulted in large size metabolites which could not pass-through glomerular filtration, then accumulate in the glomerular tufts and peritubular renal capillaries, causing chronic toxicity in kidney including, necrosis of the epithelial lining of the renal tubules and severe interstitial nephritis with thickening and sclerosis of the Bowman’s capsule and the surrounding renal tubules (Yun et al., 2015; Iavicoli et al., 2016). All these lesions were confined mainly in the renal cortex, as the proximal tubules are the main site for xenobiotic biotransformation, and therefore it is susceptible to chemical insult (Lock and Reed, 1998). In accordance with the histopathological changes in lungs, treatment with three chemicals was not toxic at low dose. On the other hand, metalaxyl showed slight pulmonary changes in the rats treated with medium and high dose, meanwhile malathion and cymoxanil resulted in more severe pulmonary changes in the groups treated with medium and high doses. Few studies revealed the respiratory effects of workers involved with pesticides, even though some pesticides may result in impairment of pulmonary function, development of chronic bronchitis, as well as impaired respiratory muscle function (Zuskin et al., 2008). The obtained pulmonary lesions might be attributed to the breakdown of the alveolar epithelial/endothelial barrier and the exudative inflammatory infiltrate into the lungs, which is in harmony with several previous reports (Hussain and Sultan, 2005). Adamis et al. (1999) mentioned that the pathophysiological processes leading to these inflammatory reactions remain unclear. Little is known about male reproductive damage caused by the used pesticides. Clearly, analysis of the male reproductive function after exposure to malathion, metalaxyl and cymoxanil of great importance (Bustos-Obregón, 2001; Bustos-Obregón et al., 2007). In the present study, rats treated with metalaxyl at all doses, malathion and cymoxanil at low dose showed the same histologic structure like that of control group, which is consistent with a previous study (Recena et al., 2006), suggested that metalaxyl is unlikely to cause reproductive effects. Meanwhile, rats treated with medium and high dose of malathion and cymoxanil showed dose dependent testicular changes. We assume that malathion affects germinal and somatic cells of the testis and decreases the testosterone activity, consequently, inhibited spermatogenesis through damage and vacuolation of Sertoli cells and germ cells (Steger et al., 1999; Farag et al., 2000; Mahgoub and El-Medany, 2001). Cymoxanil in high doses may resulted in inhibition of spermatogenesis in rats (Farag et al., 2000; Uzunhisarcikli et al., 2007; Khan et al., 2001).

The biochemical enzymatic variations are powerful predictive tool in assessment of toxicity (Kumari et al., 2012). Among others, liver is often a primary target organ for the toxic effect of xenobiotics. Therefore, it can be used as an index of toxicity of various toxicants. Transaminases and phosphatases are important critical enzymes in biological processes and are considered specific biochemical indicators of the liver damage (Gokcimen et al., 2007; Banaee et al., 2011). AST and ALT enzymes are important to metabolism of cellular nitrogen, liver glucose and oxidation of amino acids (Celik et al., 2009). Alkaline phosphatase plays an integral role in glycogen metabolism in the liver through stimulation of glucose synthesis to overcome energy required during stress conditions (Sayim, 2007; Fazilat et al., 2017). A shown in our results, low doses of the used chemicals and medium doses of malathion and metalaxyl did not disturb the liver function as the liver enzymes were within the normal limits with the exception of low dose of cymoxanil that showed slight increase of their activities. Meanwhile; higher doses of the used chemicals as well as the medium dose of cymoxanil showed elevation of AST, ALT and ALP level which means damage of the cell membrane of hepatocyte and as consequence leak of their cytosolic enzymes into blood. Elevation of ALT activity appears to reflect hepatic disease more specifically than AST values. The activity of either enzyme, particularly AST, may be elevated also in extra-hepatic disease. However, the elevation of AST and ALT, along with the elevation of ALP activities, may reflect some necro-inflammatory disease of the liver (Morowati, 1997; Kaya et al., 2015; Agrahari et al., 2007).

It should be stressed that Acetylcholine esterase is a neurotransmitter responsible for the hydrolysis of acetylcholine to choline at the synapses and the neuromuscular junction and has been considered as an excellent enzymatic marker for altering brain neural function (Cheng et al., 2020; Kumari et al., 2012). In the present study, all used chemicals showed dose dependent decreased activity of ACHE which was more obvious with cymoxanil. We assume that, the interaction of the used chemicals with AChE causing alterations in the cell membrane permeability and inducing inhibition. These results are consistent with findings of many researchers who reported that the most prominent clinical effects of poisoning with organophosphorus compounds are related to their inhibition of the activity of blood cholinesterase, leading to the accumulation of acetylcholine at cholinergic synapses which causes constant acetylcholine receptor triggering, resulting in consequent signs of neurotoxicity (Timur et al., 2003; Hazarika et al., 2003). The kidneys possess most of the common xenobiotic metabolizing enzymes, and is thus able to make an important contribution to the body’s metabolism of drugs and foreign compounds (Lock and Reed, 1998). Creatinine is a byproduct of skeletal muscle metabolism of creatine, and cleared from the blood plasma in the kidney at an approximately constant rate, primarily by filtration through the glomerulus (Mage et al., 2004). According to the present results, low doses of the all chemicals used in our study and medium doses of malathion and metalaxyl did not show any increase in the creatinine level more than that of the control group. Meanwhile; higher doses of the malathion, cymoxanil and metalaxyl as well as the medium dose of cymoxanil showed elevation of the creatinine level, indicating the impairment of the glomerular function and tubular damage in the kidneys and accumulation of creatinine in the bloodstream (Lock and Reed, 1998; Eddleston et al., 2002).

CONCLUSION

Give the above information, this study demonstrated that 21 daily repeated low dose of malathion, metalaxyl and cymoxanil pesticides was asymptomatic and target biochemical enzymes and the observed values were near to the control ones. In addition, histopathological changes in various tissues of treated rats were mostly insignificant with these low doses. In stark contrast, high dose treated rats exhibited adverse signs and symptoms of toxicity. Cymoxanil was highly toxic in all used doses than those of malathion and metalaxyl. Metalaxyl has no effect on reproductive organs while medium and high doses of malathion and cymoxanil resulted in testicular dege,neration and inhibited spermatogenesis. We assumed that, reported tissue necrosis in different organs of the high dose treated rats resulted in defects in cell membrane permeability, consequently, changes in biochemical enzymes of these tissues which are good biomarkers for studies of toxic tissue injury. The recorded toxicity of the used compounds at these low concentration levels could urge the governments for more restrictive regulations to investigate the effects of carcinogenesis for each pesticide to be safe for specific applications.

ACKNOWLEDGEMENT

This work was supported by grants from the Taif University Researchers Supporting Program (project number: TURSP-2020/151), Taif University, Saudi Arabia.

Statement of conflict of interest

The authors have declared no conflict of interest.

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Pakistan Journal of Zoology

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Vol. 54, Iss. 6, Pages 2501-3000

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