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RESEARCH ARTICLE

 

Antifertility Effects of Rhizome of Curcuma longa on Seminal Parameters of Swiss Albino Male Mice

 

Anita Raj Hembrom*, Aarti Verma, V.N. Singh

University Department of Zoology, T.M. Bhagalpur University, Bhagalpur– 812007, Bihar, INDIA

*Corresponding Author E-mail: leoannie83@gmail.com

 

ABSTRACT:

The effects of aqueous extract of rhizome of Curcuma longa on the seminal parameters of Swiss Albino male mice were investigated in this study. 36 mice were divided into six groups of six mice each with one group serving as control. Distilled water (0.1 ml) was administrated orally to control group while remaining five groups were fed with 0.1 ml (500 mg/kg BW/day) aqueous extract of rhizome of Curcuma longa for 10, 20, 30, 40 and 50 days. After completion of respective days, controls along with treated mice were sacrificed and semen from caudal epididymal part was assessed for seminal parameters such as sperm counts, motility of spermatozoa, seminal pH and mortality of the sperms. Sperm counts, sperm motility and seminal pH of cauda epididymis shows highly significant decline during 30 to 50 days treatment (p<0.001) than the control while mortality of spermatozoa increases significantly (p<0.001) than the control group of mice. Such significant alteration suggest that aqueous extract of rhizome of Curcuma longa produced adverse effects in seminal parameters and thus cause infertility among the treated groups of mice.

 

KEYWORDS: Curcuma longa, seminal parameters, contraception.


 

 

INTRODUCTION:

Population explosion imposes an extra burden on the community and it is one of the leading causes of poverty and pollution in developing countries like India. Herbal contraceptives were used even by the primitive people of ancient civilizations to control fertility and prevent pregnancy 1. Though, the conventional medicine has discovered some important antifertility agents for female, there are no methods available for male contraception except for the barrier method, withdrawal and vasectomy. Numerous herbs have been used historically to control fertility. Several plant products inhibit male and female fertility and may be developed into contraceptives 2, 3. Treatment with such plant materials results in infertility by reducing the sperm count, motility, fertility and viability as well as increasing the amount of abnormal sperm.

 

 

 

 

Received on 30.01.2015       Modified on 25.02.2015

Accepted on 19.03.2015      © RJPT All right reserved

Research J. Pharm. and Tech. 8(4): April, 2015; Page 404-406

DOI: 10.5958/0974-360X.2015.00068.2

 

 

 

Curcuma longa (turmeric) is a tall herb belonging to the family of Zingiberaceae of monocotyledons. The active principle obtained from the rhizome of the plant turmeric is curcumin. The rhizome shows some medicinal properties like Anti-inflammatory4, hypolipidemic5, anti-cancerous6, antibacterial7, antiviral8 etc. Curcuma longa has been reported to possess antifertility activity9-12. Various extracts of Curcuma longa rhizome have been reported to cause significant decline in pregnancies in female rats 13. Petroleum ether and aqueous extract of turmeric rhizome exhibit 100% antifertility activity in female rats14. The aqueous and alcoholic extracts of Curcuma longa has also been reported to inhibit completely the fertility with reduction of sperm count and motility and germ cell populations in male rats15,16.

 

In this present investigation an attempts have been made to study the anti-fertility effects of rhizome of Curcuma longa on the physical parameters of the sperm of caput epididymis of Swiss Albino male mice.

 

 

MATERIALS AND METHODS:

36 healthy and fertile adult male Swiss albino mice of body weight 25-30 g were taken from the animal house of the University Department of Zoology, T.M. Bhagalpur University, Bihar for experiment. All experimental animals maintained in normal animal husbandry condition were kept separately and were divided into six groups each consisting of six mice. One group was considered as control group while rest five were considered as experimental groups.

 

The dried rhizomes of Curcuma longa were purchased from the local market and were identified by the Department of Botany of T.M. Bhagalpur University, Bihar. These rhizomes were grinded, sieved and 1.5g fine powder was dissolved in 10ml of distilled water. The control group mice were fed 0.1ml distilled water and experimental mice were fed 0.1ml aqueous extract of Curcuma longa for 10, 20,30, 40 and 50 days respectively (500 mg/kg BW/day) orally with the help of gastric catheter. After completion of each respective day control along with experimental mice were killed by cervical dislocation. For seminal parameters assessment, both the caput were taken out and teased in 2ml of normal saline. Seminal content were sieved by a metallic net to avoid any other tissue contamination. Sample was stained with eosin and counting of sperms was done with the help of haemocytometer after the Method of Eliasson 17. During the course of study motility, mortality and caudal seminal pH were also studied. Motility of spermatozoa was observed after the Method of Tijee and Oentoeng 18. For statistical analysis data obtained were analyzed by Student’s t test.

 

RESULTS:

In the present investigation oral feeding of extract of rhizome of Curcuma longa causes significant decline in seminal parameters like sperm count (p<0.001), sperm motility (p<0.001) and seminal pH (p<0.001) of mice than the control. However the mortality of spermatozoa shows significant increase (p<0.001) than the control. As indicated in the Table 1, sperm count, sperm motility and seminal pH shows highly significant decrease during 30 to 50 days (P<0.001) among Curcuma longa treated group of mice than the control. While mortality of spermatozoa in caudal semen shows highly significant increased after 30 to 50 days (P<0.001) treatment than the control group.

 

DISCUSSION:

As indicated in Table-1 Curcuma longa rhizome shows antifertility effects in Swiss Albino male mice. Male mice treated with Curcuma longa oral dose of 0.1ml per day shows significant reduction in sperm counts than the control group of mice. Curcuma longa rhizome extract cause significant reduction in the androgen level 19 and thus affect the whole process of spermatogenesis causing significant decrease in sperm count. This indicates direct interference with testicular spermatogenic elements in the treated group of mice. Sperm motility is one of the important parameter in evaluating the fertilization ability of the ejaculated spermatozoa. Reduction in the sperm motility suggests alteration in process of sperm maturation in the epididymis which depends on the circulating androgen level. Significant decrease in the motility of spermatozoa in the treated groups of mice is due to anti-androgenic effects of the Curcuma longa rhizome causing immobilization or weakening of sperm cells.  Curcuma longa rhizome treatment also causes significant decrease in the seminal pH of cauda epididymis. This reduction in seminal pH also leads to decrease in the sperm motility as spermatozoa are very fragile at lower pH 20. Significantly higher mortality of spermatozoa in Curcuma longa rhizome treated mice is may be due to lower seminal pH and decreased motility of the spermatozoa 21, 22.

 

The present study thus concluded that the aqueous  extract of Curcuma longa rhizome show the antifertility effects in male mice by significantly decreasing sperm counts, sperm motility and seminal pH and cause significantly higher mortality of spermatozoa. As these parameters are very important in evaluating the fertile status of the male subject alteration in these seminal qualities by the treatment shows antifertility effects and can be used as one of oral contraceptive agents for fertility control among male subjects.

 

 


 

 

 

TABLE -1 Showing the effects of aqueous extract of rhizome of Curcuma longa on seminal quality of mice.

Groups

Sperm counts (×104sperms/ml)

Sperm motility ( in per cent)

Sperm mortality (in per cent)

Seminal pH

Control (6)

216.26±5.56

84.12±2.16

14.23±1.67

7.23±0.17

10 days treatment  (6)

178.54±3.67*

72.45±3.11*

28.12±2.26*

6.62±0.12*

20 days treatment  (6)

142.30±2.45**

54.32±1.57**

56.35±2.11**

5.74±0.07**

30 days treatment  (6)

107.23±4.58***

43.56±1.65***

68.18±1.87***

5.22±0.19**

40 days treatment  (6)

86.17±3.75***

35.21±3.28***

75.24±0.98***

5.04±0.05***

50 days treatment  (6)

63.20±3.19***

28.18±2.31***

87.20±1.93***

4.73±0.03***

Data presented as Mean± SEM.  *, **, ***, shows significance at 0.1, 0.01 and 0.001 levels with the value in control. Numbers within parenthesis denote number of samples.


 

 

ACKNOWLEDGEMENT:

The authors are thankful to the Head of the Department, University Department of Zoology, T. M. Bhagalpur University Bhagalpur for providing necessary laboratory facilities.

 

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