Research Article

 

Study the Effects of Follicular Size on some Biochemical Follicular Fluid Composition in She Camel (Camelus Dromedarius)

 

Mayada S. Hassan1*, Ali J. Al-Nuaimi1, Ali M. Al-Yasari2, Yasser J. Jameel1

1College of Veterinary Medicine, University of Kerbala, Kerbala, Iraq; 2College of Veterinary Medicine, Al-Muthana University, Muthanna, Iraq.

 

Editor | Kuldeep Dhama, Indian Veterinary Research Institute, Uttar Pradesh, India.

Received | March 06, 2018; Accepted | May 28, 2018; Published | July 25, 2018

*Correspondence | Mayada S Hassan, College of Veterinary Medicine, University of Kerbala, Kerbala, Iraq; Email: [email protected]

Citation | Hassan MS, Al-Nuaimi AJ, Al-Yasari AM, Jameel YJ (2018). Study the effects of follicular size on some biochemical follicular fluid composition in she camel (Camelus dromedarius). Adv. Anim. Vet. Sci. 6(8): 341-346.

DOI | http://dx.doi.org/10.17582/journal.aavs/2018/6.8.341.346

ISSN (Online) | 2307-8316; ISSN (Print) | 2309-3331

Copyright © 2018 Hassan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

 

Introduction

 

Camel is the unique animal that can live for several weeks without water. Camels are providing milk, hid and meat though a harsh and severe conditions. Moreover, it is used in racing and competition. There are two species of camel included in the genus Camelus. The first species is Camelus dromedaries, the dromedary or one-humped camel, the world population of which is estimated to be 15,368,000, with approximately 80% in Africa and 20% in Asia. The second species is C. Bactrians, the bactrian or two-humped camel, of which there are 1.7 million in their natural habitat in Asia (Al Salihi, 2016; Wardeh, 2004). The breeding of the local camelids is seasonal that start at autumn and increase drastically until the end of winter, meanwhile, it decrease significantly at spring and summer (El-Harairy et al., 2010). The follicular wave is a term replace the estrous cycle. It reflex the physiological, structural and behavior changes that occur during identified period between one ovulation and another because camels are induced ovulation. Besides, the ovulatory activities are only limited during the follicular changes (Padalino et al. 2016). The formation of follicular fluid is starting inside the ovary follicle earlier during its development (Bodhaganahalli et al., 2015). It produces from local substances produce locally, and part of this fluid is filtrated from blood serum that related with the metabolic activities of follicular cell (Gerard et al., 2002). Therefore, the compositions of follicular fluid are alike but not identical to blood plasma (Nishimoto et al., 2009). The ovary cells produce soluble substance like steroids hormone, growth factors (Fortune et al., 2004) inhibition factors (Aruna kumari et al., 2007), ionic and fat substances (Nandi et al., 2008), as well as some of minerals and salts (Sharma and Vasta, 1998). All these substances play important role in the metabolic activities of the ovary cells. Consequently, the functional status of the follicles andthe follicular fluid has an important vital role on the ovary cells that referred to the functional status of the follicle (Abdoon, 2001).The follicular fluid has biological activities, it is providing the internal environment for growing of ova and granular cells and protect the ova from the external condition. It is a good media and contains fat, steroids, amino acid and different protein and minerals. This substance provide an environment that provide fat, steroids and amino acids and different protein that provide a good environment for maturation of ova and effect on the conception (El-Shahat et al., 2013). The follicular fluid has the ability to keep the Meiosis of the egg in silent stage and protect the released egg from analysis during fertilization (Chang et al., 2005), and raising the attractiveness, movement and hat reaction of the sperm (Somfai et al., 2012). Follicular fluid is also playeda big role in auto-organization (Autocrine) and (Paracrine) of follicular cells, moreover it regulates the maturity of the cytoplasm and nucleus (Cytoplasm) of the egg and ovulation (Campbell, 2009). Knowledge of the follicular fluid components can give information about the needs of the growth and maturity of the follicles and eggs, moreover it is used as a guide to configure an active complement culture medium for maturity and identify the requirements of egg development (Zeidan et al., 2011). The study of follicular fluid in she camels is benefited the improving of in vitro maturation of the egg (IVM) (El-Hassanein et al., 2010). The metabolic activities and characteristic of follicular cell wall during its growth and development are changeable, and variations in its biochemical compositions and size are expected (Ali et al., 2011). Consequently, this study was designed to estimate the concentrations of metabolic andionic constituents including cholesterol, glucose, total protein and Calcium, Sodium and Potassium of the follicular fluid and its relation to the follicular size of she camels.

 

Materials and Methods

 

Collection of Follicular Fluid

The study was conducted in the laboratories in the Faculty of Veterinary Medicine/ University of Kerbala during the period extended from 1/10/2017 until 31/12/2017. Hundred ovaries were collected from 50 adult, (4-10) years old she camels that slaughtered at Al Najaf province abattoir during the breeding season. All these animals were in good healthy with a normal genital tract according to post-slaughter examination. The ovaries collected and placed in a plastic bag containing the normal phosphate buffered saline (PBS) (0.9%).Then, the bag was placed in a cool box and immediately transferred to the laboratory within two hours. In the laboratory, all ovaries were washed twice with PBS and placed on the filter sheets to absorb the excess water (Nandi et al., 2007). Subsequently, the follicles were removed from each other. The follicles of each ovary were measured by the Vernier calipers (Nichi-Japan) and were classified according to these measurements into two categories, the small and large groups with (3-9 mm) and (10-19mm) in diameter respectively. The follicular fluids were collected separately from each animal in each groups and placed in sterilized plastic tube and kept at -4 0 C for further analysis.

 

Biochemical Analysis of Follicular Fluid

The samples of the follicular fluid were analyzed to measure the concentration of the metabolic and ionic components in both groups. A commercial kit from RANDOX-kit-England was used to estimate the concentration of glucose and total protein using spectrophotometer-PD303-Germany the optical method that read at 546 nanometers wavelength. A commercial kit, Cromatest-kit-Spain was used to estimate the cholesterol concentration using optical spectrometer and 500 nanometers wavelength. The Biomaghreb-kit-Tunisia was used to determine the ions concentration using the optical spectrometer that read at 500 nm, 550 nm and 578 nm wavelength for sodium, calcium and potassium ions respectively.

 

Statistical Analysis

Complete randomized design was used to investigate the effect of the follicular size on the metabolic and ionic components concentration level. The mean differences between the averages using a multiplicity test (Duncan, 1955) to compare the differences between the averages. Statistical analysis of data was done according to SAS program (SAS, 2004).

 

Results and discussion

 

A significant increase (P<0.05) in the concentration of cholesterol of the follicular fluid was appeared with increase in the follicular size (Table 1). Its concentrations in the small and large follicles were 5.22 ± 0.40 mg / dL and in 7.54 ± 0.03 mg / dL respectively. The follicular cholesterol is derived from two sources, the acetate in the follicular granular cells and from the lipo-proteins of the blood plasma (Nandi et al., 2007). Cholesterol is considered as the primary substance for the building of the lipid hormones, besides the follicular fluid contains only high-density lipoproteins (HDL). Therefore, the follicular granular cells are depended on the cholesterol derived from these plasma-derived fats by crossing the basement membrane of its cells (Mishra et al., 2003). The low-density lipoproteins (LDL) molecules was lack of in the follicular fluid because its own a large size molecules that cant cross the blood vessel- follicular wall barriers (Clarke et al., 2006). The granular cells need cholesterol during its growth and multiplication. Therefore, it is withdraw from follicular fluid that led to decrease its concentration in the small size follicle. Nonetheless, when the size of follicle enlarged, its cells multiplication are decreased and lead to release cholesterol into the follicular fluid that use in the formation of lipid hormones (Su et al., 2008). The results of the current study are agreed with previous studies in she camel, buffalo and sheep that done by Albomohsen et al. (2011); Arshad et al. (2005) and Nandi et al. (2007) respectively. Meanwhile, the results of the current study are incompatible with previous reports in she camel, buffalo and goats that done by Rahman et al. (2008) and Abd Ellah et al. (2010) and Deshpande and Pathak (2010) respectively.

 

A significant increase (P<0.05) was appeared in the concentration of the follicular glucose in relation with increasing of follicular size. Its concentrations were 43.64 ± 4.76 mg / dl and 71.32 ± 10.08 mg / dL in small follicles and large follicles respectively. Glucose plays an important role for the ovarian metabolism because it acts as an important energy source for the ovary via anaerobic metabolism pathway that leads to formation of lactate (Boland et al., 1994; Rabiee et al.,1999). In small follicle, the significant increase in the glucose concentration may be due to lack of its metabolism and consumption by the few numbers of granular cells in compare to large follicles (Nandi et al., 2007; Leroy et al., 2004). However, other researcher found that high permeability of blood vessel- follicle wall barriers during the follicular growth led to filtrate more glucose from blood plasma into follicular fluid (Ying et al., 2011; Nishimoto et al., 2006). Moreover, Nishimoto et al. (2006) described the importance of glucose concentration in the growth media necessary for in vitro development and maturity of eggs. These observations are indicating to the harmful effects of decreasing and increasing glucose concentration on the growth and maturity of the egg and lead to incomplete maturation cell’s nucleus. The results of the current study are compatible with previous study in camels (Padalino et al., 2016) and disagreed with (Rahman et al., 2008) , who mentioned that the level of glucose was relatively high in the small follicles in compare to the large follicles in camelus dromedaries she camel. This variations may be occurred due species differences in different countries and even in the same country (Khanna et al., 2004). The results of this study are also in agreement with results in another species of animals as buffalo (Arshad et al., 2005), cattle (Leroy et al., 2004), sheep (Nandi et al., 2007) and goats (Herrick et al., 2006).

 

A significant decrease (P <0.05) in the total protein concentration with the increase in the size of the follicle is also appeared in Table 1. Its concentrations in follicular fluid was 6.14 ± 0.19 g/dL in small follicle, while its concentration decreased to 4.63 ± 0.13 g/dL in large follicle. The follicle needs a protein at the beginning of its formation to build up the multiple layers of granular cells and the cells surrounding the egg. Therefore, this process make the follicle needs a lot of protein that willdraw from the blood serum and excreted in the follicle and led to increase its concentrations in the small follicles (Chang et al., 2005). The lipoprotein are secreted from follicular granular cells and are involved in the new follicular formation and its blood vessels, and linear division of egg before ovulation. Therefore, it will increase at the beginning of the formation of the small follicle, thus increase in its follicular fluid (Hunter et al., 2004). However, the decreasing of protein concentration in the large size follicle was the increasing in the production of lipid hormones, that need binding proteins, therefore its consume is decrease in large follicles (Kiker et al., 2005). Moreover, the results of the current study are in agreement withprevious studies in camels (Rahman et al., 2008; Albomohsen et al., 2011), nevertheless it is incompatible with (Bodhaganahalli et al., 2015) in camels. Meanwhile, these results are agreed with the results reported in buffalo (Thangavel and Nayeem, 2004), cows (Leroy et al., 2004) and goats (Singh et al., 1999) differ with (Arshad et al., 2005), but are disagreed with (Nandi et al., 2007) in sheep and buffalo (Arshad et al., 2005).

 

Table 1: shows the concentration of metabolic components in follicular fluid of small and large follicles of the local camels

 

Large follicle (10-19 mm)	Small follicle (3-9 mm)	Composition (Metabolites)
7.54 ± 0.03 (A)	5.22 ± 0.40 (B)	Cholesterol (mg/dl)
71.32 ± 10.08 (A)	43.64 ± 4.76(C)	Glucose (mg/dl)
4.63 ± 0.13 (B)	6.14 ± 0.19 (A)	Total protein (g/dl)

 

Values with different letters within the same row are significantly different (P <0.05)

 

Table 2 ahows the concentration of ionic components small and large follicular fluid of local camels. The level of calcium ion concentration are significantly (P <0.05) affected by the follicular size. Its concentration was increased with the increase of follicular size. The calcium concentrations were 2.25 ± 0.96 mmol/L. and 3.45 ± 1.09 mmol/L. in the follicular fluid of the small and large follicles respectively. Calcium plays an important role in the production of lipid hormones of the developing follicles and it regulates the secretion of breeding hormones necessary for ovaries and ovulation (Iwata et al., 2004). Moreover, calcium ions isinvolved in the formations of estrogen. The level of this hormone is increased during follicular development and consequently, require large quantities of calcium ions that withdraw from blood inside the follicular fluid, then raising its calcium concentration (Nandi et al., 2007). The results of the current study are agreed with previous studies in camels (AlFattah et al., 2012), buffalo (Kaur et al.,1997), sheep (Nandi et al., 2007) and goats (Sava et al., 2005), while it is incompatible with (Arshad et al., 2005) in sheep.

 

The concentration of sodium ion was affected significantly (P <0.05) with variations of the follicular size. Its concentrations was 93.33 ± 4.75 mmol/L in small follicle size. Meanwhile, it was increased with increasing of follicular size that reached 145.96 ± 4.26 mmol/L. Sodium ion has a relation with vitality of the follicle and its activities in the production of estrogen that has the ability in retained sodium inside the cells (Nandi et al., 2007). The size of follicle was increased with its growth continuity because the movement of water from blood into follicular fluid. However, this process requires osmosis process across cell wall that increase with the elevation of sodium ions in the large follicle (Sharma et al., 1995). The results of the present study are agreed with previous studies in camels (Al Fattah et al., 2012), cattle (Iwata et al., 2004), buffalo (Kaur et al.,1997), goats (Bordoloi et al., 2001) and sheep (Nandi et al., 2007). While, these results are incompatible with (Rabiee et al.,1999) in cattle and (Arshad et al., 2005) in buffalo.

 

The concentration of potassium ions was significantly reduced (P <0.05) with the increase of follicular size. Its concentration was 12.96 ± 0.68 mmol/L in the fluid of small follicular size. However, its concentration was significantly decreased in to 6.12 ± 0.57 mmol / L inthe fluid of large follicular size. The decreasing of the potassium ion concentration is related with the follicle development that lead to increase glucose consumption. This process lead to move potassium ions from extracellular spaces to intracellular space and thus reduces its concentration in the follicular fluid when follicular size enlarge. The concentration of potassium ions in the follicular fluid revealed high significance in compare to its concentration in the serum accompanied with missing a correlation between them indicated that Potassium ion may be excreted locally in the follicular fluid (Leroy et al., 2004; Al Fattah et al., 2012). These results are in agreement with (Al Fattah et al., 2012) in camels and (Arshad et al.,2005) in buffalo and (Leroy et al., 2004) in cattle and (Nandi et al., 2007) in sheep.

 

Table 2: Shows the concentration of ionic components small and large follicular fluidof local camels

 

Large follicle (10-19 mm)	Small follicle (3-9 mm)	Composition (Ions mmol/L)
3.45 ± 1.09 (A)	2.25 ± 0.96 (B)	Calcium
145.96 ± 4.26 (A)	93.33 ± 4.75 (C)	Sodium
6.12 ± 0.57 (B)	12.96 ± 0.68 (A)	Potassium

 

Values with different letters within the same row are significantly different (P <0.05)

 

In conclusion, this study approved the variations in the concentration of metabolic and ionic components of follicular fluids in relation to the follicular size and its development stage. The results of this study can be consider in the formulation of egg culture media use in the in vitro fertilization.

 

Acknowledgements

 

We would like to thank The College of Veterinary Medicine/Al Muthanna University for accepting our article in 2nd Colloquium for Camel Research and giving us this opportunity to express our science.

 

Conflict of interest

 

This research is a personal non-profit work and there is no conflict of interest.

 

Authors Contribution

 

Both of Mayada S. Hassan and Ali J. Al-Nuaimiare are responsible for animal work and samples collection. Ali M. Al-Yasari and Yasser J. Jameel are responsible for data analysis, writing correction and proof reading.

 

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