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IOSR Journal Of Pharmacy
(e)-ISSN: 2250-3013, (p)-ISSN: 2319-4219
www.iosrphr.org Volume 5, Issue 3 (March 2015), PP. 1-3
1
Dynamics of Combined Oral Contraceptive: A Study of Some
Cytokines in Female Wistar Rats
Toryila J.E.1
, Amadi K. 2
, Odeh S.O. 2
, Egesie U.G. 2
, Adelaiye A.B. 1
,
Atsukwei A 3
, Achie L.N 1
1,
Human Physiology Department, Faculty of Medicine, ABU Zaria.
2,
Human Physiology Department, Faculty of Medical SciencesUnijos.
3,
Department of Physiology, Faculty of Basic Medical Sciences, Bingham University,Karu, Nasarawa State
Abstract: Oral contraceptives are a simple form of contraception used by women worldwide. The oral
contraceptive is one of the greatest and most influential developments of the twentieth century. It is regarded as
the most reliable method of contraception, and one of the easiest. They are widely available in most pharmacies
and chemist shops. This research priority included efforts to discover the effect of combined oral
contraceptives(COC) (DUOFEM) on some cytokines in female wistar rats. Eighty (80) female wistar rats aged
10-12 weeks weighing 180-250 g were used for the study. They were divided into four groups of 20 rats each
comprising 10 treated and 10 control rats. The treated rats received 0.6mg/kg body weight of COC
intragastically for 36, 48, 60 and 72 days in five-day cycles (four-day treatment with one-day break). The COC
was given intragastically in 5-day cycles (4-day treatment with 1-day break). All controls were given fresh
water at ad libitum daily for the period of the experiment.The blood sample was drawn into plain tubes..An
enzyme-linked immunosorbent assay (ELISA) was used for the quantitative determination of
Erythropoietin(EPO), interleukin-6 (IL-6) and interleukin-11 (IL-11). There were significant decrease in
interleukin-6 (IL-6) and interleukin-11 (IL-11),but no significant change in Erythropoietin.While further study is
necessary, current evidence suggest that COC (DUOFEM) use provides contraceptives benefits with minimal
potential adverse effects in healthy users.
Keywords: Combined Oral Contraceptives, Cytokines, Wistar rats.
I. INTRODUCTION
Global family planning programmes have been in existence in the developed world for several decades
and are primarily designed to supply couples with the methods of family planning that best suit their needs.
Birth control is a major factor in public health and welfare, preserving the general and reproductive health of
women and allowing them to choose the movement of a planned pregnancy (WHO, 2009). The World Health
organization (WHO) and other global organizations are seeking ways to increase the amount of information and
access people have to contraception and other resources related to family planning all round the world.
Contraception is an important aspect of reproductive health and plays a major role in the
prevention of unwanted pregnancy arising from rape for example. It is therefore a significant factor in reduction
of induced abortion rate and improvement in maternal health care (Echendu, et al., 2011). Oral contraceptives
had been reported to have beneficial effects in reducing the incidence of pelvic inflammatory disease, decrease
risk of ectopic pregnancy, benign breast lesions, ovarian and endometrial cancers, protection against
osteoporosis and rheumatoid arthritis among the users (Vessey, 1995).
Oral contraceptives are sometimes used to treat heavy or irregular menstruation and endometriosis.
Oral contraceptive agents can also be used in hormonal replacement therapy, and in the emergency post-coital
contraception. Oral contraceptive decreases the risk of ectopic pregnancy, benign breast lesions, ovarian and
endometrial cancers, and offer protection against osteoporosis and rheumatoid arthritis (Rosing, 1999).
Despite the general acceptability and the obvious advantages that have been attributed to oral
contraceptives use, some serious side effects have been reported in women taking them. Studies have indicated a
relationship of oral contraceptives use and cardiovascular disease, altered levels of coagulation factors,
thrombosis, platelet changes, atherosclerosis and multiple sclerosis.Estrogen has been known to have
prothrombin effects and elevates cardiovascular and venous thromboembolism risk(Margoliset al,2007).
Cytokines are peptides that have a fundamental role in communication within the immune system and
in allowing the immune system and host tissues cells to exchange information. Cytokines are nonantibody
proteins that can be made by awide range of cell types. About 30 cytokines are recognized, including the
interleukins (IL-1 to IL-24), tumor necrosis factors (TNFs), and transforming growth factors(TGF Beta 1–3). In
general, cytokines are low molecularweight (200 amino acids) and have specific receptors.Collectively,
cytokines mediate cellular intercommunications via autocrine, paracrine, or endocrine mechanisms.Cytokine
Dynamics Of Combined Oral Contraceptive: A Study Of Some Cytokines In Female Wistar Rats.
2
actions are the result of a complex network, often involving feedback loops and cascades, the overall response
being dependent on the synergistic or antagonisticactions of its various components.
The haemopoietic growth factors and cytokines are the soluble regulators of blood cell production and
are produced by several cell types in different sites in the body (Almediaet al.Haemopoietic growth factors
regulate the proliferation, differentiation and maturation of haemopoietic precursor cells. These include IL-3,
IL-6, IL-11, GM-CSF (Bernadette et al., 2012).
Erythropoietin (EPO) is a cytokine and a glycoprotein hormone that is essential for the proliferation
viability and terminal differentiation of erythroid progenitor through erythropoietin receptor (EPOR) expression
( Wu et al, 1995).Epo is produced mainly in the kidney and to some extend in the liver, brain and uterus. Epo is
shown to act an non-haematopoietic cells such as central organs neverous system, the heart and the other organs
and tissues resulting in tiuse protection (Rei et al, 2000 ). Epo has antiapoptopic, antioxidant and anti-
inflammatory effects .The effects of COCs on several haemorheological and haemostatic parameters has been
reported (Akhigbe, et al, 2008). Recently, EPO has emerged as a multifunctional growth factor that plays a
significant role in the nervous.
II. MATERIALS AND METHODS
The combined oral contraceptive used is DUEFEM®. They were obtained from family clinic, Ahmadu
Bello University Teaching Hospital, Shika-Zaria, and from the Society for Family Health (SFH) Abuja, Nigeria.
COCs DUOFEM® tablets which combined ethinylestradiol and Norgestrel were manufactured by Wyeth Ayerst
(USA) and packed and marketed by the Society for Family Health, Lagos, Nigeria. DUOFEM® is a child
spacing pill containing ferrous fumarate tablets. Each DUOFEM cycle contains 28 pills; each white tablet
contains 0.3mg Norgestrel and 0.03mg Ethinglestradiol and each brown tablet contains 75mg ferrous fumarate.
DUOFEM® has a molecular weight of 312.4458g/mol (Chitturi etal,2003).Eighty (80) female wistar rats aged
10-12 weeks weighing 180-250 g were used for the study. They were divided into four groups of 20 rats each
comprising 10 treated and 10 control rats. The treated rats received 0.6mg/kg body weight of COC
intragastically for 36, 48, 60 and 72 days in five-day cycles (four-days treatment with one-day break).
The COC was given intragastically in 5-day cycles (4-day treatment with 1-day break). All controls
were given fresh water ad libitum daily for the period of the experiment. Animals were sacrificed after
anaesthesia with chloroform and 5ml of blood was obtained via cardiac puncture and placed in plain bottles.
Interleukin 11 and 6 (IL-11, IL-6), erythropoietin (EPO) and liver function tests were determined by ELISA
method.
III. RESULTS
Erythropoietin (EPO)was not significantly increase in EPO in all the treated groups( A;12.3±1.9,
B;14.4±1.5,C; 10.8±1.3and D;10.7±1.2), compared to the controls (P<0.431, P<0.324, P<0.057 and P<0.108)
.Interleukin 6 (IL-6)was significantly decreased in treated groups C;34.7±8.0 and D;26.1±1.5compared to the
controls (37.7±1.8and47.1±9.8).Interleukin 6 (IL-6)was significantly increased in treated group A;30.9±7.2 and
B; 30.7±8.7compared to controls (20.8±1.2 and 26.0±1.6). Interleukin 11 (IL-11)was significantly decreased in
treated groups C(37.9±1.3) and D (46.8±1.8) compared to the controls (P<0.005 & P<0.002). There was no
significant increase in IL-11 in treated groups A and B compared to the controls (P<0.086 and P<0.987).
The effects of combined oral contraceptives on some cytokines in female wistar rats
IV. DISCUSSION
There was no significant change in serum erythropoietin level in all the controls. This finding is
contrary to that of Prechileet al. (1972) who found that estradiol benzoate inhibited the production of
erythropoietin (EPO). Erythropoietin promotes the survival, proliferation and differentiation of erythrocytic
Groups IL-11 (ng/L) IL-6 (ng/L) EPO (iu/L)
A (36 Days) 45.2±7.6 30.9±7.2 12.3±1.9
Control 42.4±9.6 20.8±1.2 10.5±1.2
P-value 0.086 0.001 0.431
B (48 Days) 51.1±9.1 30.7±8.7 14.4±1.5
Control 50.1±9.1 26.0±1.6 11.9±1.1
P-value 0.987 0.005 0.057
C (60 Days) 37.9±1.3 34.7±8.0 10.8±1.3
Control 41.7±1.0 37.7±1.8 11.1±1.4
P-value 0.005 0.050 0.324
D (72 Days) 46.8±1.8 26.1±1.5 10.7±1.2
Control 49.0±2.2 47.1±9.8 12.4±1.2
P-value 0.002 0.005 0.108
Dynamics Of Combined Oral Contraceptive: A Study Of Some Cytokines In Female Wistar Rats.
3
progenitors. EPO deficiency is the primary cause of the anaemia in chronic kidney disease. It appears COC has
little or no effect in EPO production. Decreased RBC count in this study may not be as a result of COC effect on
EPO. There was a significant decrease in serum level of interleukin-6 (IL-6) and a slight decrease in serum
interleukin-11 (IL-11). Estrogen is able to decrease IL-6 expression by blocking the osteoblast’s synthesis of IL-
6 receptors IL-11 and IL-6 are haemopoiesis-promoting factors capable of enhancing the growth of myeloid,
erythroid and megakaryocytic progenitor cells. They are capable of mediating a complex array of pro- and anti-
inflammatory effects. IL-6 produces C-Reactive Protein (CRP) which leads to cardiovascular risk.
Experimental studies have shown strong correlations between the risk of cardiovascular diseases and
inflammatory markers such as CRP and tissue neurosis factor-α (TNF α) (Subhadeepet al., 2008). IL-6 is a
pleotropic cytokine which stimulates B-lymphocyte and T-lymphocyte differentiation, and activates
macrophages and NK cells. The finding of reduced serum IL-6 is in agreement with the finding of Straub et al.
(2000) who reported decrease serum level of IL-6 in menopausal women taking hormonal replacement therapy.
IL-6 plays important physiologic roles, deregulatedoverproduction of IL-6 causes various pathologic
conditions, including autoimmune, inflammatory, and lymphoproliferative
disorders. It has been shown that IL-6 is involved in immuneinflammatory diseases such as rheumatoid arthritis
(RA), Castlemandisease, juvenile idiopathic arthritis (JIA), and Crohndisease. Elevatedserum IL-6 has been
observed in patients with these diseases andthe IL-6 levels correlate with disease activity (Uson et al, 1997 ).
REFERENCE
[1]. There Were Significant Decrease In Interleukin-6 (IL-6) And Interleukin-11 (IL-11),But No Significant Change In
Erythropoietin.While Further Study Is Necessary, Current Evidence Suggest That COC (DUOFEM) Use Provides Contraceptives
Benefits With Minimal Potential Adverse Effects In Healthy Users.
[2]. References
[3]. Dan Rosing (1999). Effects Of Oral Contraceptives On Haemostasis And Thrombosis, Am. J. Orbst. Gyn; 180(6): 5375 – 5382.
[4]. Akhigbe R.E., Azeez M.O., Ige S.F., Oyeyipo L.P., Ajao F.O. And Alade A.O. (2008). Haematological Effects Of Long-Term
Administration Of Combined Oral Contraceptive In Rats.International Journal Of Pharmacology, 4(5): 403-406.
[5]. Akinsanya M A, Adeniyi T T, Ajai GO, Oyedele MA (2010). Effect Of Vitamin E And Folic Acid On Some Antioxidant Activities
Of Female Wistar Rats Administered Combined Oral Contraceptives.
[6]. African Journal Of Biochemistry Research , 4 (10):Pp 238-242.
[7]. 4.Vessy M.P. (1995). Endometrial And Ovarian Cancer And Oral Contraceptives: Findings In A Large Cohort Study. British
Journal Of Cancer, 71: 1340-1342.
[8]. World Health Organization (2009). Hormonal Contraception And Liver Disease. Contraception 80; 325 – 326.
[9]. Subhadeep C., Olga L., And Sandra T.D. (2008). Estrogen Is A Modulator Of Vascular Inflammation. IUBMB Life, 60(6): 376-
382.
[10]. Bernadette F.R., Gorge A.F. And Eliane M.K. (2012). Haematology: Clinical Principles And Applications (4th
Ed.). China: Elsevier
Saunders.
[11]. Margolis K.L., Adami H.O.,Luo J., Ye W., Weiderpass E. (2007). A Prospective Study Of Oral Contraceptive Use And Risk Of
Myocardial Infarction Among Swedish Women.Fertil.Steril.,88: 310-316
[12]. Rei Y., Sachiko M., Shigeka V. And Okamura (2002) Erythropoietin And Erythropoitin Receptor Expression In Human
Endometrium Through The Menstrual Cycle.
[13]. Wu H., Liu X., Jaenisch R. And Lodish H.F. (1995). Generation Of Committed Erythoid BFU-E Progenitors Does Not Require
Erythropoietin Or The Erythropoietin Receptor. Cell,83: 59-67.
[14]. Chitturi S, Farrell GC 2013). Adverse Effects Of Hormones And Hormone Antagonists On The Liver. In, Kaplowitz N, Deleve LD,
Eds. Drug-Induced Liver Disease. 3rd Ed. Amsterdam: Elsevier, , Pp. 605-620. (Review Of Hepatotoxicity Of Oral Contraceptive
Steroids Including Cholestasis, Vascular Disorders, Benign Tumors And Hepatocellular Carcinoma.
[15]. Uson J; Balsa A; Pascualsalcedo D; Cabezas J A; Gonzaleztarrio JM; Martinmola E; Fontan G (1997)
Soluble Interleukin-6 (Il-6) Receptor And Il-6 Levels In Serum And Synovial-Fluid Of Patients With Different Arthropathies
Journal Of Rheumatology.
[16]. ST R AU BR H ,C U TO L OM ( 2000). I Nvolvement Ofthehy P O T H A L A M I C - P I T U I T A Ry - A D Re N A L / Go N A
D A Laxis And The Peri P H E Ral Nervous System Inrheumatoid Arthritis:Viewpoint Based On Asystemic Patho
[17]. Genetic Rolearthritis Rheum1; 44: 493-507

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A05320103

  • 1. IOSR Journal Of Pharmacy (e)-ISSN: 2250-3013, (p)-ISSN: 2319-4219 www.iosrphr.org Volume 5, Issue 3 (March 2015), PP. 1-3 1 Dynamics of Combined Oral Contraceptive: A Study of Some Cytokines in Female Wistar Rats Toryila J.E.1 , Amadi K. 2 , Odeh S.O. 2 , Egesie U.G. 2 , Adelaiye A.B. 1 , Atsukwei A 3 , Achie L.N 1 1, Human Physiology Department, Faculty of Medicine, ABU Zaria. 2, Human Physiology Department, Faculty of Medical SciencesUnijos. 3, Department of Physiology, Faculty of Basic Medical Sciences, Bingham University,Karu, Nasarawa State Abstract: Oral contraceptives are a simple form of contraception used by women worldwide. The oral contraceptive is one of the greatest and most influential developments of the twentieth century. It is regarded as the most reliable method of contraception, and one of the easiest. They are widely available in most pharmacies and chemist shops. This research priority included efforts to discover the effect of combined oral contraceptives(COC) (DUOFEM) on some cytokines in female wistar rats. Eighty (80) female wistar rats aged 10-12 weeks weighing 180-250 g were used for the study. They were divided into four groups of 20 rats each comprising 10 treated and 10 control rats. The treated rats received 0.6mg/kg body weight of COC intragastically for 36, 48, 60 and 72 days in five-day cycles (four-day treatment with one-day break). The COC was given intragastically in 5-day cycles (4-day treatment with 1-day break). All controls were given fresh water at ad libitum daily for the period of the experiment.The blood sample was drawn into plain tubes..An enzyme-linked immunosorbent assay (ELISA) was used for the quantitative determination of Erythropoietin(EPO), interleukin-6 (IL-6) and interleukin-11 (IL-11). There were significant decrease in interleukin-6 (IL-6) and interleukin-11 (IL-11),but no significant change in Erythropoietin.While further study is necessary, current evidence suggest that COC (DUOFEM) use provides contraceptives benefits with minimal potential adverse effects in healthy users. Keywords: Combined Oral Contraceptives, Cytokines, Wistar rats. I. INTRODUCTION Global family planning programmes have been in existence in the developed world for several decades and are primarily designed to supply couples with the methods of family planning that best suit their needs. Birth control is a major factor in public health and welfare, preserving the general and reproductive health of women and allowing them to choose the movement of a planned pregnancy (WHO, 2009). The World Health organization (WHO) and other global organizations are seeking ways to increase the amount of information and access people have to contraception and other resources related to family planning all round the world. Contraception is an important aspect of reproductive health and plays a major role in the prevention of unwanted pregnancy arising from rape for example. It is therefore a significant factor in reduction of induced abortion rate and improvement in maternal health care (Echendu, et al., 2011). Oral contraceptives had been reported to have beneficial effects in reducing the incidence of pelvic inflammatory disease, decrease risk of ectopic pregnancy, benign breast lesions, ovarian and endometrial cancers, protection against osteoporosis and rheumatoid arthritis among the users (Vessey, 1995). Oral contraceptives are sometimes used to treat heavy or irregular menstruation and endometriosis. Oral contraceptive agents can also be used in hormonal replacement therapy, and in the emergency post-coital contraception. Oral contraceptive decreases the risk of ectopic pregnancy, benign breast lesions, ovarian and endometrial cancers, and offer protection against osteoporosis and rheumatoid arthritis (Rosing, 1999). Despite the general acceptability and the obvious advantages that have been attributed to oral contraceptives use, some serious side effects have been reported in women taking them. Studies have indicated a relationship of oral contraceptives use and cardiovascular disease, altered levels of coagulation factors, thrombosis, platelet changes, atherosclerosis and multiple sclerosis.Estrogen has been known to have prothrombin effects and elevates cardiovascular and venous thromboembolism risk(Margoliset al,2007). Cytokines are peptides that have a fundamental role in communication within the immune system and in allowing the immune system and host tissues cells to exchange information. Cytokines are nonantibody proteins that can be made by awide range of cell types. About 30 cytokines are recognized, including the interleukins (IL-1 to IL-24), tumor necrosis factors (TNFs), and transforming growth factors(TGF Beta 1–3). In general, cytokines are low molecularweight (200 amino acids) and have specific receptors.Collectively, cytokines mediate cellular intercommunications via autocrine, paracrine, or endocrine mechanisms.Cytokine
  • 2. Dynamics Of Combined Oral Contraceptive: A Study Of Some Cytokines In Female Wistar Rats. 2 actions are the result of a complex network, often involving feedback loops and cascades, the overall response being dependent on the synergistic or antagonisticactions of its various components. The haemopoietic growth factors and cytokines are the soluble regulators of blood cell production and are produced by several cell types in different sites in the body (Almediaet al.Haemopoietic growth factors regulate the proliferation, differentiation and maturation of haemopoietic precursor cells. These include IL-3, IL-6, IL-11, GM-CSF (Bernadette et al., 2012). Erythropoietin (EPO) is a cytokine and a glycoprotein hormone that is essential for the proliferation viability and terminal differentiation of erythroid progenitor through erythropoietin receptor (EPOR) expression ( Wu et al, 1995).Epo is produced mainly in the kidney and to some extend in the liver, brain and uterus. Epo is shown to act an non-haematopoietic cells such as central organs neverous system, the heart and the other organs and tissues resulting in tiuse protection (Rei et al, 2000 ). Epo has antiapoptopic, antioxidant and anti- inflammatory effects .The effects of COCs on several haemorheological and haemostatic parameters has been reported (Akhigbe, et al, 2008). Recently, EPO has emerged as a multifunctional growth factor that plays a significant role in the nervous. II. MATERIALS AND METHODS The combined oral contraceptive used is DUEFEM®. They were obtained from family clinic, Ahmadu Bello University Teaching Hospital, Shika-Zaria, and from the Society for Family Health (SFH) Abuja, Nigeria. COCs DUOFEM® tablets which combined ethinylestradiol and Norgestrel were manufactured by Wyeth Ayerst (USA) and packed and marketed by the Society for Family Health, Lagos, Nigeria. DUOFEM® is a child spacing pill containing ferrous fumarate tablets. Each DUOFEM cycle contains 28 pills; each white tablet contains 0.3mg Norgestrel and 0.03mg Ethinglestradiol and each brown tablet contains 75mg ferrous fumarate. DUOFEM® has a molecular weight of 312.4458g/mol (Chitturi etal,2003).Eighty (80) female wistar rats aged 10-12 weeks weighing 180-250 g were used for the study. They were divided into four groups of 20 rats each comprising 10 treated and 10 control rats. The treated rats received 0.6mg/kg body weight of COC intragastically for 36, 48, 60 and 72 days in five-day cycles (four-days treatment with one-day break). The COC was given intragastically in 5-day cycles (4-day treatment with 1-day break). All controls were given fresh water ad libitum daily for the period of the experiment. Animals were sacrificed after anaesthesia with chloroform and 5ml of blood was obtained via cardiac puncture and placed in plain bottles. Interleukin 11 and 6 (IL-11, IL-6), erythropoietin (EPO) and liver function tests were determined by ELISA method. III. RESULTS Erythropoietin (EPO)was not significantly increase in EPO in all the treated groups( A;12.3±1.9, B;14.4±1.5,C; 10.8±1.3and D;10.7±1.2), compared to the controls (P<0.431, P<0.324, P<0.057 and P<0.108) .Interleukin 6 (IL-6)was significantly decreased in treated groups C;34.7±8.0 and D;26.1±1.5compared to the controls (37.7±1.8and47.1±9.8).Interleukin 6 (IL-6)was significantly increased in treated group A;30.9±7.2 and B; 30.7±8.7compared to controls (20.8±1.2 and 26.0±1.6). Interleukin 11 (IL-11)was significantly decreased in treated groups C(37.9±1.3) and D (46.8±1.8) compared to the controls (P<0.005 & P<0.002). There was no significant increase in IL-11 in treated groups A and B compared to the controls (P<0.086 and P<0.987). The effects of combined oral contraceptives on some cytokines in female wistar rats IV. DISCUSSION There was no significant change in serum erythropoietin level in all the controls. This finding is contrary to that of Prechileet al. (1972) who found that estradiol benzoate inhibited the production of erythropoietin (EPO). Erythropoietin promotes the survival, proliferation and differentiation of erythrocytic Groups IL-11 (ng/L) IL-6 (ng/L) EPO (iu/L) A (36 Days) 45.2±7.6 30.9±7.2 12.3±1.9 Control 42.4±9.6 20.8±1.2 10.5±1.2 P-value 0.086 0.001 0.431 B (48 Days) 51.1±9.1 30.7±8.7 14.4±1.5 Control 50.1±9.1 26.0±1.6 11.9±1.1 P-value 0.987 0.005 0.057 C (60 Days) 37.9±1.3 34.7±8.0 10.8±1.3 Control 41.7±1.0 37.7±1.8 11.1±1.4 P-value 0.005 0.050 0.324 D (72 Days) 46.8±1.8 26.1±1.5 10.7±1.2 Control 49.0±2.2 47.1±9.8 12.4±1.2 P-value 0.002 0.005 0.108
  • 3. Dynamics Of Combined Oral Contraceptive: A Study Of Some Cytokines In Female Wistar Rats. 3 progenitors. EPO deficiency is the primary cause of the anaemia in chronic kidney disease. It appears COC has little or no effect in EPO production. Decreased RBC count in this study may not be as a result of COC effect on EPO. There was a significant decrease in serum level of interleukin-6 (IL-6) and a slight decrease in serum interleukin-11 (IL-11). Estrogen is able to decrease IL-6 expression by blocking the osteoblast’s synthesis of IL- 6 receptors IL-11 and IL-6 are haemopoiesis-promoting factors capable of enhancing the growth of myeloid, erythroid and megakaryocytic progenitor cells. They are capable of mediating a complex array of pro- and anti- inflammatory effects. IL-6 produces C-Reactive Protein (CRP) which leads to cardiovascular risk. Experimental studies have shown strong correlations between the risk of cardiovascular diseases and inflammatory markers such as CRP and tissue neurosis factor-α (TNF α) (Subhadeepet al., 2008). IL-6 is a pleotropic cytokine which stimulates B-lymphocyte and T-lymphocyte differentiation, and activates macrophages and NK cells. The finding of reduced serum IL-6 is in agreement with the finding of Straub et al. (2000) who reported decrease serum level of IL-6 in menopausal women taking hormonal replacement therapy. IL-6 plays important physiologic roles, deregulatedoverproduction of IL-6 causes various pathologic conditions, including autoimmune, inflammatory, and lymphoproliferative disorders. It has been shown that IL-6 is involved in immuneinflammatory diseases such as rheumatoid arthritis (RA), Castlemandisease, juvenile idiopathic arthritis (JIA), and Crohndisease. Elevatedserum IL-6 has been observed in patients with these diseases andthe IL-6 levels correlate with disease activity (Uson et al, 1997 ). REFERENCE [1]. There Were Significant Decrease In Interleukin-6 (IL-6) And Interleukin-11 (IL-11),But No Significant Change In Erythropoietin.While Further Study Is Necessary, Current Evidence Suggest That COC (DUOFEM) Use Provides Contraceptives Benefits With Minimal Potential Adverse Effects In Healthy Users. [2]. References [3]. Dan Rosing (1999). Effects Of Oral Contraceptives On Haemostasis And Thrombosis, Am. J. Orbst. Gyn; 180(6): 5375 – 5382. [4]. Akhigbe R.E., Azeez M.O., Ige S.F., Oyeyipo L.P., Ajao F.O. And Alade A.O. (2008). Haematological Effects Of Long-Term Administration Of Combined Oral Contraceptive In Rats.International Journal Of Pharmacology, 4(5): 403-406. [5]. Akinsanya M A, Adeniyi T T, Ajai GO, Oyedele MA (2010). Effect Of Vitamin E And Folic Acid On Some Antioxidant Activities Of Female Wistar Rats Administered Combined Oral Contraceptives. [6]. African Journal Of Biochemistry Research , 4 (10):Pp 238-242. [7]. 4.Vessy M.P. (1995). Endometrial And Ovarian Cancer And Oral Contraceptives: Findings In A Large Cohort Study. British Journal Of Cancer, 71: 1340-1342. [8]. World Health Organization (2009). Hormonal Contraception And Liver Disease. Contraception 80; 325 – 326. [9]. Subhadeep C., Olga L., And Sandra T.D. (2008). Estrogen Is A Modulator Of Vascular Inflammation. IUBMB Life, 60(6): 376- 382. [10]. Bernadette F.R., Gorge A.F. And Eliane M.K. (2012). Haematology: Clinical Principles And Applications (4th Ed.). China: Elsevier Saunders. [11]. Margolis K.L., Adami H.O.,Luo J., Ye W., Weiderpass E. (2007). A Prospective Study Of Oral Contraceptive Use And Risk Of Myocardial Infarction Among Swedish Women.Fertil.Steril.,88: 310-316 [12]. Rei Y., Sachiko M., Shigeka V. And Okamura (2002) Erythropoietin And Erythropoitin Receptor Expression In Human Endometrium Through The Menstrual Cycle. [13]. Wu H., Liu X., Jaenisch R. And Lodish H.F. (1995). Generation Of Committed Erythoid BFU-E Progenitors Does Not Require Erythropoietin Or The Erythropoietin Receptor. Cell,83: 59-67. [14]. Chitturi S, Farrell GC 2013). Adverse Effects Of Hormones And Hormone Antagonists On The Liver. In, Kaplowitz N, Deleve LD, Eds. Drug-Induced Liver Disease. 3rd Ed. Amsterdam: Elsevier, , Pp. 605-620. (Review Of Hepatotoxicity Of Oral Contraceptive Steroids Including Cholestasis, Vascular Disorders, Benign Tumors And Hepatocellular Carcinoma. [15]. Uson J; Balsa A; Pascualsalcedo D; Cabezas J A; Gonzaleztarrio JM; Martinmola E; Fontan G (1997) Soluble Interleukin-6 (Il-6) Receptor And Il-6 Levels In Serum And Synovial-Fluid Of Patients With Different Arthropathies Journal Of Rheumatology. [16]. ST R AU BR H ,C U TO L OM ( 2000). I Nvolvement Ofthehy P O T H A L A M I C - P I T U I T A Ry - A D Re N A L / Go N A D A Laxis And The Peri P H E Ral Nervous System Inrheumatoid Arthritis:Viewpoint Based On Asystemic Patho [17]. Genetic Rolearthritis Rheum1; 44: 493-507