Iraqi J Pharm Sci, Vol.32( 1 ) 2023                                               Sub-chronic effect of different doses of diclofenac sodium                                            

DOI: https://doi.org/10.31351/vol32iss1pp227-236 

227 
 

Sub-Chronic Effect of Different Doses of Diclofenac Sodium on Female 

Reproductive System in Rats 

Bedoor A. Salim*, Muhsin S.Ghalib** and Ausama Ayob Jaccob**,2 
*Ministry of Health and Environments , Maysan Health Directorate, Baby and Maternity hospital, Maysan, Iraq.  
**Department of pharmacology and Toxicology, College of pharmacy, University of Basra, Basra, Iraq. 

Abstract 
Non-steroidal anti-inflammatory drugs (NSAIDs) are widely utilized drugs in today's world. These 

medications are well-known for their anti-inflammatory and analgesic properties. The goal of this study was to suggest 

and explain the sub- chronic effects of low and high doses of diclofenac on female reproductive system in rats. A total 

of 24 female rats were divided into 4 groups, six rats in each. The first group was given distilled water as a control for 

35 days, the second and third groups were given diclofenac (1 mg/kg) and (5 mg/kg) for 35 days respectively. The fourth 

group was given a combination of diclofenac and mefenamic acid for 35 days. Hormonal, biochemical, and 

hematological tests were performed.  Low dose diclofenac showed no significant change regarding luteinizing hormone 

(LH), progesterone, prolactin, and glutathione, but an increase in follicle stimulating hormone ( FSH), and decrease in 

prostaglandin E2 PGE2 and estrogen compared to control group were documented. In contrast, high dose diclofenac 

alone or combined with mefenamic acid showed   significant impact on female reproductive system documented by 

biochemical and histopathological evaluations. At hematological levels diclofenac decrease red blood cells (RBC), 

hemoglobin concentration (HGB), and platelet account but no change in the total white blood cells (WBC) were found. 

Sub-chronic use of diclofenac sodium (DS) alone or in combination with mefenamic acid have a deleterious impact on 

the female reproductive system, oxidative stress and hematological parameters. 
Keywords: NSAIDs, Diclofenac sodium, Female reproductive toxicity. 

 ناث أل الجهاز التناسلي على الصوديوم ديكلوفيناك من مختلفة لجرعات التأثير دون المزمن

 الجرذان 
  ** يعقوبايوب  أسامة و  **غالب محسن صغير ,*عباس سالم بدور

 

 العراق.  ، ميسان ، مستشفى الطفل والوالدة  ، وزارة الصحة, دائرة صحة ميسان *

 .العراق البصرة،  جامعةالبصرة،  كليةالصيدلة،  فرع االدوية والسموم، **
 

 الخالصة
المضادة لاللتهابات والمسكنات. تستخدم مضادات االلتهاب غير الستيرويدية على نطاق واسع في عالم اليوم. تشتهر هذه األدوية بخصائصها  

نثى في الفئران. كان الهدف من هذه الدراسة هو اقتراح وشرح التأثيرات دون المزمنة للجرعات المنخفضة والعالية من ديكلوفيناك على الجهاز التناسلي لأل

ألولى أعطيت الماء المقطر كعنصر تحكم ، المجموعة مجموعات ، ستة فئران في كل مجموعة. المجموعة ا  4أنثى من الجرذان إلى    24تم تقسيم إجمالي  

مجم / كجم( على التوالي. المجموعة الرابعة أعطيت مزيج من ديكلوفيناك وحمض الميفيناميك لمدة   5مجم / كجم( و )  1الثانية والثالثة أعطيت ديكلوفيناك )

،   LH، اك أي تغيير معنوي فيما يتعلق بـ. لم تظهر الجرعات المنخفضة من ديكلوفينيوما. تم إجراء االختبارات الهرمونية والكيميائية الحيوية والدموية 35

هرمون االستروجين مقارنة بمجموعة    البروستاكالندين و  وانخفاض في ،    FSHالبروجسترون ، البروالكتين ، والجلوتاثيون ، ولكن تم توثيق زيادة في  

يكلوفيناك بمفردها أو مع حمض الميفيناميك تأثيًرا كبيًرا على الجهاز التناسلي لألنثى موثقًا من خالل  التحكم. في المقابل ، أظهرت الجرعات العالية من د

، وحساب الصفائح الدموية الهيموغلوبينالتقييمات البيوكيميائية والتشخيص المرضي . في مستويات الدم ، يقلل ديكلوفيناك من عدد كرات الدم الحمراء ،  

له تأثير ضار على حمض الميفينامك  وحده أو باالشتراك مع  لدايكلوفيناك  االستخدام شبه المزمن  .  WBCلى أي تغيير في إجمالي  ولكن لم يتم العثور ع

 .الجهاز التناسلي األنثوي ، واإلجهاد التأكسدي والمعايير الدموية

 . لألنثى التناسلية السمية ،  الصوديوم ديكلوفيناك ، الستيرويدية غير  االلتهاب مضادات: المفتاحية الكلمات  

Introduction 
Nonsteroidal anti-inflammatory drugs 

(NSAIDs) are a family of pharmaceuticals 

authorized by the FDA for the treatment of different 

diseases as antipyretic, anti-inflammatory, and 

analgesic (1). They are indicated for muscular 

discomfort, dysmenorrhea, arthritic diseases, gout, 

and as opioid-sparing medications in some acute 

traumatic diseases (2,4). At the mechanistic levels, 

NSAIDs inhibit the production of prostaglandins by 

blocking the cyclooxygenase (COX) enzymes. 

 

 

COX enzymes are divided into two types: COX-1 

and COX-2. The first one is constitutively 

responsible for the creation of prostaglandins 

necessary for organ function, gastric protection, 

platelet aggregation, and vasoconstriction. The 

COX-2 isoform is inducible and found in the 

kidneys and vascular endothelium, and it is only 

created when the body is inflamed (5).  

 

 

 
1Corresponding author E-mail: ausama.jaccob@uobasrah.edu.iq 

Received: 14/4 / 2022  

Accepted: 26/ 6 / 2022 

 

Iraqi Journal of Pharmaceutical Science 

 

https://doi.org/10.31351/vol32iss1pp227-236


Iraqi J Pharm Sci, Vol.31(2) 2022                                                 Sub-chronic effect of different doses of diclofenac sodium                                          

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Prostaglandins are made from the 

polyunsaturated phospholipid (arachidonic acid) by 

a series of multistep enzymatic processes, such 

enzymes are targeted by a variety of medications, 

the most common of which being (NSAIDs). It 

appears that chronic use of NSAIDs might have a 

negative impact on bodily tissues including renal 

dysfunction, blood pressure, hepatic damage, 

platelet inhibition, gastrointestinal, cardiovascular 

and reproductive system as recently studied 

organs(6,7). 

Diclofenac sodium (DS) is one of the most 

commonly prescribed analgesic. It is a phenylacetic 

acid derivative that has been used as human 

medicine for many years to treat rheumatoid 

arthritis, osteoarthritis, ankylosing spondylitis, and 

primary nocturnal enuresis (8). In the short term, it 

might potentially be used to treat acute 

musculoskeletal injuries and dysmenorrhea (9). The 

availability of DS as an over-the-counter medication 

may lead to its misuse, resulting in gastrointestinal, 

liver, renal, and neurological consequences(10–12). 

Furthermore, it can be seen that the hematological 

and biochemical indicators of rats may be 

significantly affected by DS. As a consequence, it 

can be inferred that DS, at various dosages and over 

different periods, may have negative impacts on 

critical animal tissues, resulting in hematological 

disorders, hepatic and renal impairments (13). It was 

found that DS produce histological changes in the 

male rat's testicles, reduce sperms count, motility, 

viability, and significantly reduce testosterone 

level(10).  

Little data are available regarding the effect 

of NSAIDs on the female reproductive system 

(FRS), however, ovulation, whether primary or 

secondary may be affected. Normally, 

prostaglandins play an essential role in the ovulation 

process. When luteinizing hormone (LH) surges and 

progesterone levels increase before the onset of 

ovulation, prostaglandins help to facilitate ovulation 

by digesting the collagen surrounding the ovarian 

follicle and also by stimulating smooth muscle 

contraction. However, the exact mechanism by 

which prostaglandins accomplish these steps is still 

unclear and required further research to declare 

it(14).NSAIDs can cause reversible infertility in 

women due to the suppression of cyclooxygenase 

enzymes and prevent formations of prostaglandin. 

Since NSAIDs are widely used and abused in 

women during their reproductive years, it has been 

proven that these women will have "luteinized 

unruptured ovarian follicles"(15). Fortunately, natural 

ovulation was reported to be retained after these 

agents were stopped(16). Cölçimen N et al. 

investigated the morphological and prenatal follicle 

number after low dose (1mg/kg) DS administration, 

no significant differences were observed in pregnant 

rats compared to the remaining groups(17). Due to the 

limited knowledge are available on the effect of 

NSAIDs on the female reproductive system, the 

present work was designed to evaluate the possible 

effect of subchronic administration of different 

doses of DS alone or in combination with 

mefenamic acid on the female reproductive system 

in rats. 

Materials and methods 
Materials  

Diclofenac sodium obtained from AL-

Fayhaa pharmaceutical company in AL-Basrah city, 

Iraq, Mefenamic acid (Ponstan Forte) tablet as 500 

mg active ingredient was purchased from (Pfizer 

manufacturing Deutschland GmbH, Betriebsstatte 

Freiburg, Germany). All hormonal analysis kits 

were purchased from Abbott Co. (USA), while 

PGE2 and GSH ELISA kits, were obtained from 

Shanghai YL Biotech Co. (China). 

Animals 

This study employed twenty-four mature 

female albino rats weighing between 150 and 250 g. 

They purchased from the Animal Holding Unit of 

the University of Basrah, The College of Veterinary 

Medicine, Iraq. The rats were maintained in plastic 

cages with a temperature of 25–30 °C and a 12-hour 

light/12-hour dark photoperiodicity. They were fed 

a standard pelletized diet and had free access to 

water daily, and were weighed before the beginning 

of the work as the starting point, then every 7days, 

and at the end of the experiment. After two weeks of 

acclimatization to the new laboratory environment, 

the rats were enrolled in the current study.  The study 

followed the National Institute of Health Guidelines 

for the Use of Laboratory Animals, and ethical 

approval was received in October/2021 from the 

Pharmacy College/University of Basrah/Ethics 

Committee 3/5/293. 

Experimental design  

Twenty-four female rats were chosen 

randomly and divided into control and three (3) 

treated groups, with six animals in each group. The 

control group received only distilled water (as a 

vehicle of diclofenac sodium) orally administered 

daily to be compared and exclude vehicle, stress, 

and environmental effects. Group 1  rats received 

1mg/kg (9) of DS gavaged daily. Group2 rats treated 

with a high dose of DS (5mg/kg) (18) were gavaged 

in a daily manner. Group3 rats received a 

combination of both DS (5mg/kg) and mefenamic 

(20mg/kg) via the oral route. All control and treated 

groups administered their scheduled doses for a 

period of 35 days as sub-chronic study model. The 

rats were weighed every 7 days, and the doses 

changed accordingly. After the last day of 

medication treatment, 5 mL of blood from each rat 

was withdrawn via posterior vena cave with a needle 

syringe while they were anesthetized with 

chloroform. Then the blood was distributed into two 

tubes one of them for hematological parameters 

evaluation, while the remaining were allowed to clot  



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and centrifuged at 10000rpm for 20 minutes, and the 

resulting serum was extracted, frozen, to be used 

later for biochemical and hormonal analysis. The 

ovaries of the rats were excised and fixed in formalin 

for histopathological investigation. 

Hormonal assay 

Serum levels of LH, FSH, progesterone, 

estradiol, and prolactin were measured using 

prepared kits of Chemiluminescent Microparticle 

Immunoassay (CMIA) for the quantitative 

determination of these hormones following the 

manufacturer's procedure while utilizing a 

diagnostic automated laboratory analyzer (Abbott 

Architect i4000, USA). 

Biochemical assay 

Serum glutathione and PGE2 were 

determined using an ELISA (enzyme-linked 

immune sorbent assay) based on the Biotin double 

antibody sandwich technology according to the 

manufacturer's instructions. 

Hematological parameters 

The anticoagulated blood was used to 

calculate the hematological parameters. red blood 

cells (RBC) count, hemoglobin (Hb) concentration, 

packed cell volume (PCV), total white blood cells 

(WBC) count, monocytes count, lymphocytes count, 

granulocytes count, platelets count, mean 

corpuscular volume (MCV), mean hemoglobin 

concentration (MCHC), and mean corpuscular 

hemoglobin (MCH) were all determined using 

automated hematology analyzer Nano 3 (GenoLab-

TEK, Windsor, Canada). 

Histopathological examination  

Ovaries of each rat were sliced into tiny 

pieces, cleaned in normal saline, and stored in 10% 

formaldehyde. A sample of tissue was dried and 

buried in paraffin before being sliced into 3–4 mm 

slices and mounted on a thin glass slide. Staining 

was done with hematoxylin and eosin (H&E), and 

then a comprehensive histopathological 

investigation was performed under supervision of 

professional pathologist.  

Statistical analysis 

One-way ANOVA analysis was used 

among groups. Then Turkey’s post-hoc analysis test 

was utilized for further assessment of data to obtain 

clear P values between groups. Data were expressed 

as Mean± SEM with p<0.05 significance. GraphPad 

Prism software (Version 6.0). 

Results 
Administration of DS for 35 days in Group 

1 and Group2 decreased body weight gain compared 

to the control group as shown in figure (1). Group3 

rats received co-treatment of DS and MA as a 

combination to evaluate the possible sub-chronic 

unwanted effect of these compounds. No changes in 

body weights were documented when correlating 

statistically between changes in body weights and 

periods of time (35 days) P=0.0687.  Compared to 

the control group, changes in body weight in Group3 

were different and no weight gain was documented, 

nevertheless, there is a significant increase in body 

weight in the remaining groups. 

 
 

Figure 1. Changes in rats body weights with 

respect to days of the experiments. No significant 

changes in body weights during time were 

documented in in group 3 P>0.05. * Represents 

significant difference in comparison to control 

P<0.05. Results are presented as Mean ± SEM 

In this study, measurement of serum PGE2as 

prognostic biomarker is important point to explain 

and correlate the relationship between NSAIDs use 

and female reproductive hormone effect. Figure (2) 

clearly proves this idea where a significant reduction 

in serum PGE2 level in group1 (treated with low 

dose DS), group2 (treated with a high  

dose of DS) P=0.0051 and group3 (treated with 

combination) P=0.0006 compared to the control 

group.  

 
Figure 2. Impact of sub-chronic use of low and 

high pharmacological doses of Diclofenac sodium 

alone (Group1, 2) and in combination with 

mefenamic acid (Group3) on serum 

concentration of prostaglandin E2 (PGE2) in rats 

(N=24). Values are expressed as Mean± SEM. 

*represent significant difference P<0.05   among 

groups. 

Serum concentrations of FSH were 

significantly elevated in all treated groups as shown 



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230 
 

in figure 3A in comparison to the control group. Rats 

ingroup1 showed the highest significant value 

compared to other treated and control groups. 

Administration of pharmacological doses of DS in 

combination with mefenamic acid significantly 

increase serum LH value in group3 as shown in 

figure 3B. Groups 1 and 2 are well-matched with the 

control group and no significant differences were 

documented.  

 
 

Figure 3. Impact of sub-chronic use of low and high pharmacological doses of Diclofenac sodium alone 

(Group1, 2) and in combination with mefenamic acid (Group3) on A: serum concentration of (FSH), B: 

serum concentration of (LH) in rats (N=24). Values are expressed as Mean± SEM. *represent significant 

difference P<0.05 among groups. ** represent significant difference P<0.01 among groups.

Serum concentrations of estrogen were 

significantly reduced in all treated groups as shown 

in figure 4A compared to normal control group. Oral 

administration of DS is associated negatively with 

serum estradiol concentrations. In contrast, 

Administration of a high pharmacological dose of 

DS in (Group2) and in combination with mefenamic 

acid (Group3) significantly increases serum 

progesterone value compared to the normal control 

group and Group1 as seen in figure 4B. Groups 1 

associated with a non-significant (P>0.05) 

compared to control. 

 
Figure 4. Impact of sub-chronic use of low and high pharmacological doses of Diclofenac sodium alone 

(Group1, 2) and in combination with mefenamic acid (Group3) on A: serum concentration of Estradiol, 

B: serum concentration of Progesterone in rats (N=24). Values are expressed as Mean± SER. *represent 

significant difference P<0.05 among groups. 

 

 

 



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Serum prolactin levels were evaluated in this work 

to obtain a complete explanation about the effect of 

NSAIDs on the female reproductive system. There 

are no significant differences were observed 

between Groups 1, 2, and control groups, all of them 

are well-matched as seen in figure 5. A significant 

reduction in serum prolactin level was detected in 

Group3 compared to the remaining group. 

 
Figure 5. Impact of sub-chronic use of low and 

high pharmacological doses of Diclofenac sodium 

alone (Group1, 2) and in combination with 

mefenamic acid (Group3) on serum 

concentration of Prolactin in rats (N=24). Values 

are expressed as Mean± SER. *represent 

significant difference P<0.05 among groups. 

Figure 6 summarizes serum concentrations of 

Glutathione in control and all studied groups. Serum 

Glutathione concentration significantly decreased in 

Group 2(rats exposed to a high pharmacological 

dose of DS) compared to the control group. No 

significant differences were documented between 

Groups1, 3, and control groups, all of them have 

comparable glutathione concentrations. 

 
Figure 6. Impact of sub-chronic use of low and 

high pharmacological doses of Diclofenac sodium 

alone (Group1, 2) and in combination with 

mefenamic acid (Group3) on serum 

concentration of Glutathione levels in 

rats(N=24). Values are expressed as Mean± SEM. 

*represent significant difference P<0.05 among 

groups. 

The microscopic finding of ovaries of control rats 

showed normal primordial follicles, primary and 

secondary follicles, Graafian's follicles, and normal 

parenchymal cells (figure 7A). In contrast to the 

treatment groups showing numerous follicles with 

thick and dark dyed granulosa and theca layers, 

Graafian follicles with pyknotic oocyte, multi 

follicles ovary, corpus luteum (CL), and asterisk 

fibrotic (figure 7B,C and D). 

Figure 7. Light micrographs of the ovary section stained with H&E X20, A) representative image showed normal 

follicle growth, primary and secondary (thick arrowhead), oocyte with healthy nucleus (thin arrow), graafian 

and corpus luteum with healthy appearance (thick arrow). B) representative image showed numerous follicles 

with thick and dark dyed granulosa and theca and layers(black arrow), Graafian follicles with pyknotic 

oocyte(thick arrowhead), multi follicles  ovary (thin arrow), corpus luteum (Cl); asterisk, fibrotic(red arrow).C) 

representative image showed numerous follicles(thin arrow), thick arrow, graafian follicles, oocyte, nucleus  with 

healthy appearance, and  Graafian follicles with pyknotic nucleus(whit arrow).D) representative image showed  

(white arrow) graafian follicles with healthy appearance, thick and dark dyed granulosa and theca and 

layers(blue arrow), corpus luteum with asterisk, fibrotic(red arrow). 



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Blood was collected form rats and characteristic 

complete blood count of all groups are summarized 

in Table (1). The concentrations of WBC were 

comparable in all treated and control groups. The 

finding of differential cell count showed that the 

percent of lymphocyte, and MID% were 

significantly reduced in Group3 and Group1 

respectively compared to control. No significant 

differences were documented in granulocyte 

concentration in all treated and control groups. The 

red blood cell count and hemoglobin values were 

negatively associated with NSAIDs administration 

in all treated groups compared to control. Data on 

MCV, MCH, and MCHC give us an idea about the 

amount and average concentration of hemoglobin in 

RBC. Significant reduction in their values was 

detected in Groups 1 and 2 and 3 in comparison to 

that in control group. Results of the present work 

indicate a significant reduction in platelet count in 

all Groups that received DS alone or in combination 

with mefenamic acid compared to the control group.  

 

Table 1. Impact of sub-chronic use of low and high pharmacological doses of Diclofenac sodium alone 

(Group1, 2) and in combination with mefenamic acid (Group3) on complete blood count in rats (N=24). 

Values are expressed as Mean± SEM. *represent significant difference P<0.05 compared to control. 
 

parameter Control 

Mean± SER 

Group1 

Mean± SER 

Group2 

Mean± SER 

Group3 

Mean± SER 

P-Value 

WBC (10^3/Ul) 10.8± 1.45 11.29 ± 2.35 13.8 ± 1.52 12.25 ± 1.46 P<0.05 

Lym% 78.3±2.19 71.95± 4.65 72.65±3.53 60.37± 3.81* P>0.05 

Gran% 13.46 ±2 12.86 ± 2.57 16.5 ±3.01 17.23± 2.158 P<0.05 

Mid% 8.23 ±0.53 5.18 ± 2.15* 10.83 ± 1.02 7.4± 0.86 P>0.05 

RBC(10^6/Ul) 6.93± 0.15 5.16 ± 0.17* 5.43± 0.22* 6.22 ± 0.09* P>0.05 

HGB( g/dL) 13.22±0.2 11.08 ± 0.24* 11.08± 0.57* 11.5± 0.15* P>0.05 

HCT % 38.76 ± 1.1 34.06 ± 0.71 34.4± 1.96 36.26 ± 0.27 P<0.05 

MCV(fL) 65.75±1.75 59.72± 0.41* 59.25± 1.6* 59.52±0.53* P>0.05 

MCH(pg) 20.81 ±0.97 21.55± 0.54 19.81 ± 0.4 18.25±0.2* P>0.05 

MCHC(g/dL) 33.3±0.31 32.5± 0.1 33.18 ± 0.07 33.55±0.1 P<0.05 

RDW-CV % 13.18±0.27 15.01± 0.66* 14.46 ± 0.44 13.85± 0.32 P<0.05 

RDW-SD(fL) 34.38±1.17 39.81± 1.46* 34.38 ±1.08 32.15± 1 P<0.05 

PLT(10^3/uL) 567.7±20.28 421.5±23.42* 466.7±19.96* 399.3 ± 20.23* P>0.05 

MPV(fL) 8.75±0.522 7.06 ± 0.25* 7.08 ± 0.13* 6.96 ±0.16 * P>0.05 

PDW(fL) 8.75±0.52 8.08 ± 0.46 8.35± 0.31 8.13 ± 0.27 P<0.05 

PCT% 0.3618±0.007 0.29 ± 0.01 0.46 ± 0.05 0.519±0.05 * P>0.05 

P-LCR% 11.41±1.6 8.9± 1.45 8.5± 0.6 8.18 ±0.99 P<0.05 

P-LCC10^9/L) 62.5±8.58* 34.67±3.49 59± 7.96 58.83 ± 7.687 P>0.05 

 

Discussion 
 (FRS) maybe affected by different 

toxicants that may in turn induce direct or indirect 

adverse outcomes. Certain chemicals digested and 

bio-transformed locally into toxic free radicals, 

whereas others cause toxic damage through 

hormonal regulation (19).DS is one of the most 

commonly used NSAIDs among women of 

reproductive age for the management of a range of 

women's illnesses, including dysmenorrhea and 

menorrhagia(20). Chronic use and abuse of NSAIDs 

may lead to an unexpected effect on FRS, from this 

the current work was intended to explain how the  

sub-chronic use of DS affected the female 

reproductive system in rats. 

An experiment in this study has shown 

administration of DS resulted in a reduced body 

weight gain in group1 (received low dose of DS) and 

group 2 (received a high dose of DS) as compared to 

the control group. Decrease in food intake, gastric 

discomfort associated with NSAIDs causes stomach 

and intestinal lesions as the most prominent adverse 

effects are the principal reasons for our results. Our 

findings are seen to be consistent with different 

studies, Elliott SN et al showed that use of DS in  

dose (5 mg/kg), bodyweight growth was 

significantly reduced and Alabi QK et al found the 



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233 
 

treatment of the rats with DS resulted in a reduction 

in body weight. (18,21). On other hand, other articles 

demonstrated a positive correlation between 

NSAIDs use and an increase in body weight. this 

may be explained by edema and impairment of renal 

function occurring in DS abuse (22). 

 In the current study, low and high doses of 

DS (Group1 and 2) alone or when combined with 

mefenamic acid (Group3) diminished serum PGE2 

concentration significantly compared to the control 

group. Mechanistically, This reduction can be 

explained due to inhibition of PGE2 synthesis both 

centrally and peripherally by competitive reversible 

inhibition of COX enzymes (23). These findings align 

with Nakatsugi S et al. who found that NSAIDs have 

the ability to inhibit the PGE2 production through 

COX-2 from exogenous and endogenous 

arachidonic acid (24). Furthermore, Abdel- Halem 

MS et al found that DS was a powerful inhibitor of 

PGE2 biosynthesis in the brain (25).  

Measurement of serum prostaglandins in 

this experiment is important to correlate and further 

interpret our finding regarding the impact of 

NSAIDs abuse on FRS. 

 Oral administration of DS alone and in combination 

with MA resulted in a significant elevation in serum 

FSH levels in comparison to the control group, the 

highest significant value seen in group 1. On the 

other hand, significant elevation in serum LH level 

in group 3, compared to the remaining groups. 

Measurement of serum menotropins levels in 

relation to other female hormones are interesting 

because the impact of negative and positive 

feedback mechanisms of all these hormones cascade 

is considered the key to discussing our results. 

Unfortunately few articles have been carried out on 

this field, however, these hormonal changes are 

similar to that found by. Ji K et al found a significant 

increase in transcription of FSHr and LHr, genes 

after exposure to NSAIDs (26). In contrast, some 

studies showed treatment with NSAIDs causes a 

decrease in both serum LH and FSH levels (7), or 

non-significant changes in the serum levels of FSH 

and LH (27,28).The cystic appearance of the treatment 

animals' ovaries compared to the normal control 

group confirm these results. These histopathological 

changes was due to the failure of ovulation of a 

certain number of graafian follicles that had been 

converted into luteinized unruptured follicles (29). 

Inhibition of PG synthesis in the preovulatory 

follicles by NSAIDs hampered the completion of the 

ovulatory process, resulting in follicular rupture 

failure and thus cyst formation(30).Our findings 

matched those of  Tomioka RB et al, who reported 

an increase in LUF syndrome in Juvenile idiopathic 

arthritis ( JIA) patients on NSAIDs (15). Also Jesam 

C et al who showed Non-steroidal anti-

inflammatory medicines (meloxicam or rofecoxib) 

are known to have comparable effects on ovulation 

when used systemically over several days. These 

medications caused luteinized un-ruptured follicles 

(LUF), or dysfunctional, delayed ovulation (31). 

Evaluation of serum estrogen along with serum 

progesterone levels in this study are important to 

fully summarized the effect of DS on complete 

blood hormones of FRS. Serum estrogen levels were 

significantly reduced in all treated groups compared 

to the control group. Estrogen is a hormone that 

plays a major role in female reproduction. It is 

responsible for the ovulatory follicle's development,  

activating the pre-ovulatory surge of gonadotropins 

in the middle of the menstrual period, changing the 

condition of cervical mucus to make it easier for 

sperm to travel, and preparing the uterine 

endometrial lining for implantation (32). PGE2 

increases estrogen production by increasing the 

activity of aromatase, the enzyme that converts 

androgens to estrogens (33). These results are in 

agreement with Wangwa EK et al found that 

NSAIDs (Piroxicam) has been shown to have 

detrimental effects on female fertility by lowering 

levels of estrogen, progesterone, and gonadotropin, 

also Hudson AG et al found that serum estradiol 

levels in NSAID users are considerably lower than 

in non-users (7,34). Regarding progesterone levels 

assay, we found the opposite results compared to 

estrogens values. Serum progesterone levels were 

significantly elevated in both groups 2 and 3 

compared to the control group while the group1 

showed a non-significant effect because of limited 

articles talking about this project. However, drug 

molecules that inhibit PG synthesis could adversely 

affect progesterone value and consequently female 

hormones. These findings are similar to that of 

Amiridis GS et al who reported that meloxicam was 

used at various periods after insemination to reduce 

PGF2a release, raise luteal progesterone levels, and 

prevent early embryonic death (35). On other hand,  

these results disagree with previous studies that 

found NSAIDs cause a decrease in serum 

progesterone levels like Dzięcioł M et al showed 

single dose administration of meloxicam cause a 

significant drop in progesterone levels, also Amina 

S et al showed that usage of mefenamic acid cause 

the progesterone levels to drop with dose equal to 

0,5 mg/Kg 1 mg/Kg, 1,5 mg/Kg, and 2 mg/Kg(36,37). 

To complete the view about the effect of 

NSAIDs on FRS, serum prolactin levels were 

measured. A non-significant change in the serum 

prolactin levels in treated groups compared to the 

control group were obtained except in group 3 which 

showed a significant reduction in serum prolactin 

level compared to the control group. One reason for 

that was inhibition of prostaglandins (PGs) 

biosynthesis in the central nervous system (CNS), 

PGS may stimulate prolactin release in the 

hypothalamus (25). The current result comes in tune 

with previous studies that showed  DS causes a rapid 

and sustained decrease in prolactin plasma levels in 

healthy volunteers (38). In contrast, our finding was 



Iraqi J Pharm Sci, Vol.31(2) 2022                                                 Sub-chronic effect of different doses of diclofenac sodium                                          

234 
 

challenged by Adeyemi WJ et al demonstrated DS 

treatment cause an increase in the level of prolactin 

in male rats (39). 

Glutathione is the main abundant thiol anti-

oxidant in the body. It's a natural antioxidant found 

in both male and female gametes, in varying 

quantities. It has been proven that it is involved in 

the fertilization process and early embryo 

development. It protects eggs from oxidative stress 

during folliculogenesis, and as a result, egg quality 

is highly dependent on it (40). Excessive reactive 

species generation, such as reactive oxygen species 

(ROS), has been linked to diclofenac metabolism in 

vivo, resulting in oxidative stress, genomic damage, 

and cell death via apoptosis (41). In this study, there 

is a significant decrease in serum glutathione 

concentration in group 2 treated with high dose DS 

compared to the control group. These findings are 

consistent with the results that reflect high doses DS 

administration to rats lower glutathione 

concentrations significantly compared to control 

groups (10,42). 

Finally, the considerable changes in 

hematological markers in diclofenac sodium-treated 

rats might indicate toxicity. The overall WBC count 

did not change significantly in any of the treatment 

groups during this study. This is in agreement with 

previous studies (43). Although Abd-El Megid S et al 

showed that NSAIDs causes a significant decrease 

in WBC count (44). The considerable drop in white 

blood cell counts found in the treatment groups 

might be attributed to the participants' reduced feed 

consumption, as noted during the experiment. This 

is in line with previous research, which found that 

reduced feed intake had a significant influence on 

the hematopoietic system, resulting in lower 

numbers of white blood cells, platelets, and 

reticulocytes (45).The significant decrease in RBC 

and HGB levels in all treatment groups when 

compared to the control group might indicate drug-

induced toxicity, which is characterized by 

excessive red blood cell destruction and anemia (46). 

It might also be attributed to erythrocyte loss from 

gastrointestinal hemorrhage. When the body loses a 

significant amount of blood.  The results of this 

investigation are consistent with those of Orinya OA 

et al (13), and Abdel-Rahman ON et al (47). Significant 

reductions in MCV, MCH, and MCHC values were 

detected in all treated groups compared to the 

control group. Similar outcomes were observed in 

previous studies (48). Significant reduction in platelet 

count in all treated groups compared to control 

group, it's reasonable that the lower platelet count in 

this study might be due to DS's inhibitory influence 

on platelet synthesis, lowering platelet     aggregating 

strength. This is in agreement with earlier studies 
(13,49). 

In conclusion, according to the present 

finding, we can assume that sub-chronic use of DS 

alone or in combination with MA has a deleterious 

impact on the female reproductive system through 

disruption of hormonal concentrations and 

regulations, shifting the balance toward oxidative 

stress by reduction of glutathione concentrations, 

and ovarian histopathological changes. 

Furthermore, considerable reduction in leukocytes, 

RBC, hemoglobin, and platelet counts were 

documented at hematological levels 

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