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  • Short communication
  • Open Access

Immunization against recombinant GnRH-I alters ultrastructure of gonadotropin cell in an experimental boar model

Contributed equally
Reproductive Biology and Endocrinology201311:63

  • Received: 9 April 2013
  • Accepted: 10 July 2013
  • Published:



Gonadotropin cell is the main responsible for the secretion of follicle stimulating hormone (FSH) and luteinizing hormone (LH), and immunocastration reduces the concentrations of serum FSH and LH. A few studies have reported the histological structure of gonadotropin cells obtained from immunocastration animals at the light microscopy level. However, the ultrastructure of gonadotropin cells remains largely unexplored. The aim of this study was to evaluate and to compare ultrastructure of gonadotropin cell in gonadally intact boars and immunologically castrated male animals.


In this study, serum and adenohypophysis tissue were collected from nine gonadally intact boars and nine male pigs treated with recombinant gonadotropin releasing hormone I (GnRH-I). Anti-GnRH-I antibodies in serum and the ultrastructure of gonadotropin cell in adenohypophysis were determined by enzymelinked immunosorbent assay and electron microscopy, respectively. The results demonstrated that active immunization against recombinant GnRH-I increased serum GnRH-I antibody levels (P<0.05). Ultramicroscopic analysis of gonadotropin cell revealed a decrease (P<0.05) in the number and size of the large granules and small granules in the recombinant GnRH-I immunized animals.


We conclude that immunization against recombinant GnRH-I induces severe atrophy of granules in gonadotropin cell of boars, possibly reflecting GnRH-I regulation of gonadotropin cell.


  • Ultrastructure
  • Gonadotropin
  • Boar
  • Immunization
  • GnRH-I


One promising alternative to surgical castration as a method of controlling undesirable behavior and aggression that has been researched for many years [13] is active immunization against (GnRH-I). Immunological castration uses the animal’s own immune system to suppress GnRH-I and thus shut down the stimulus to the testes resulting in an inhibition of testicular function. Many researchers report that immunization against GnRH-I significantly reduce serum concentrations of FSH and LH [4, 5]. In sheep immunized against GnRH-I at prepubertal or peripubertal age, plasma LH concentrations were not restored after GnRH-I injection at a time when anti-GnRH-I antibodies are low [5, 6] or not detectable [7]. GnRH-I or eCG treatment fails to reproductive function in GnRH-I immunized ewes [8]. Therefore, these findings have led to the suggestion that active immunization against GnRH-I disrupt the secretion of the gonadotropin cell in pituitary. Previous studies on pituitary obtained from immunocastration animals at the light microscopy level [8, 9]. Nevertheless, to the best of our knowledge, there is no report to date on ultrastructural pituitary changes in the GnRH-I immunized animals. Thus, it is of interest to investigate the ultrastructure of gonadotropin cells in adenohypophysis of immunocastrated male pigs.

Fang et al. [10] used recombinant DNA technology to form maltose binding protein–gonadotropin releasing hormone I (MBP–GnRH-I6) vaccines, which had success in affecting the reproductive systems of pigs [11]. The objective of the present study was to evaluate the ultrastructure of gonadotrophin cells in MBP–GnRH-I6 immunized pigs.



Eighteen Chinese boars, reared at the DaDun Animal Farm, Shucheng, China, were used in the study. The study has been approved by Animal Care and Use Committee of Anhui Agricultural University. The animals were assigned randomly to two groups of the following treatments: MBP–GnRH-I6 immunization (n = 9) and MBP immunization (n = 9). All boars had access to food and water ad libitum.

Preparation of antigens and immunization

MBP-GnRH-I6 was prepared and using recombinant DNA techniques as has been previously described [10]. Nine milligrams of MBP-GnRH-I6 or MBP was dissolved in 9 mL phosphate-buffered saline (PBS) and 9 mL of Al(OH)3 adjuvant (Tianbang, Nanjing, China). The first immunization was administered at 9 weeks of age by intramuscular injection of 2 mL of emulsion. The booster injection was given by the same route and at the same dose 8 weeks later. The pigs were slaughtered 8 weeks after the booster immunization.

Analysis of anti-GnRH-I antibody

Blood samples were taken via the jugular vein when 9, 13, 17, 21 and 25 weeks old and centrifuged at 200 × g for 15 minutes at 4°C. Serum was harvested and stored at −80°C until assayed. The amount of anti-GnRH-I antibody in the collected serum from animals was measured as described by Fang et al. [11].

Transmission electron microscopy of thin sections

After slaughter, the tissue of adenohypophysis was fixed in 2.5% glutaraldehyde for 4 to 6 hours, and post-fixation was accomplished in 1% osmium tetroxide for 1 hour. The samples were subjected to an alcohol dehydration series (30% 15 minutes, 50% 15 minutes, 70% 6–12 hours, 80% 15 minutes, 95% 15 minutes, 100% 40 minutes). The tissues were immersed in 1, 2-epoxypropane (Lingfeng Chemical Co. Ltd) for 30 minutes, and then transferred to 1, 2-epoxypropane and resin Epon812 (1:1) for 2 hours. Samples were individually embedded in Epon812 (Serva) for 2 hours. Resin blocks were solidified at 45°C for 12 hours and 65°C for at least 48 hours. Ultrathin sections (70 nm thick) were prepared from each tissue with an ultrathin section machine (LKBNUBA, NOVA) and blade (LKB2178, knife maker II, BROMMA). Sections were stained with 1% (w/v) methanolic uranyl acetate (Lanzhou State-owned Factory 404) for 30 minutes, and then washed three times in deionized water for a total of 15 minutes, and stained with lead citrate for 30 minutes.

The sections were rinsed in a stream of distilled water and dried prior to examination. Sections were visualized on a transmission electron microscopy (JEM-1230, Japan).

Acquisition and analysis of data

Eight to 10 random sections were taken to represent tissue. The diameter and the number of the granules were measured using the specific software (Image-Pro plus 6.0). The data is expressed as mean ± standard deviation (SD). Statistical analysis was performed by the Student’s t-test. Significance was given at P<0.05.


Results showed that serum level of the antibody against MBP–GnRH-I6 in vaccinated animals was increased significantly as compared with MBP mock-immunized boars (P<0.05) (Figure 1), suggesting MBP–GnRH-I6 immunization induced a strong anti-GnRH immune response.
Figure 1
Figure 1

High anti-GnRH-I antibody concentrations in boars immunized with MBPGnRH-I6. Microwell plates were coated with recombinant GnRH-I and incubated with sera collected from boars immunized with MBP–GnRH-I6 (n = 9) and MBP (n = 9). The results (mean ± SD) shown are the absorbance at 450nm for 1:500 dilution of sera. Arrows indicate time of immunizations. One star and two stars show P < 0.05 and P < 0.01, respectively. Black square and black triangle indicate MBP-GnRH-I6 immunized animals and MBP mock-immunized boars, respectively.

A lot of large granules and small granules were found in cytoplasm of gonadotropin cell of adenohypophysis from electron microscopic images (Figure 2). The granules, round or oval in shape, main closely distributed at one side of nucleus (Figure 2). The gonadotropin cells showed evidence of severe changes in the granules. That is, the mean number and diameter of large granules and small granules in MBP mock- immunized boars (Figure 2A, C) were significantly more (P<0.05) than those of in MBP-GnRH-I6 immunized animals (Figure 2B, D) (Table 1).
Figure 2
Figure 2

Ultrastructure of the adenohypophysis showing gonadotropin cells in boars immunized with MBPGnRH-I6 (n = 9) and MBP (n = 9). A and C: MBP mock-immunized boars; B and D: MBP-GnRH-I6 immunized male pigs. Cell organs are shown as the large granules (arrows), small granules (square area), mitochondrion (t) and nucleus (N). A and B: × 6000, scale bar = 1 μm; C and D: × 10000, scale bar = 500 nm.

Table 1

The number and diameter of granules of gonadotropin cells in boars immunized with MBPGnRH-I6


Diameter of granules (nm)

The number of granules








157.75±19.45 A

26.72±4.08 A

152.56±9.78 A






All data were shown as mean ± SD. Different superscripted letters in the column indicate a significant difference (P<0.05).

In conclusion, the results of the present study demonstrate that administration of recombinant GnRH-I to boars elicits clear increase in serum antibody levels and decrease in the number and diameter of the large granules and small granules in the gonadotropin cell.




Follicle stimulating hormone


Luteinizing hormone


Maltose binding protein–gonadotropin releasing hormone I


Maltose binding protein


Recombinant gonadotropin releasing hormone I.



This work was supported by a grant from Anhui Provincial Natural Science Foundation (Grant 1208085MC39), and Specialized Research Fund for the Doctoral Program of Higher Education from Ministry of Education Science and Technology Development Center, Beijing, P. R. China (Grant 20123418110004), and National High-Tech R&D Program (2011AA100307).

Authors’ Affiliations

Anhui Provincial Laboratory of Animal Genetic Resources Protection and Breeding, College of Animal Sciences and Technology, Anhui Agricultural University, No. 130 of Changjiang West Road, 230036 Hefei, Anhui, China
Anhui Provincial Laboratory for Local Livestock and Poultry Genetic Resource Conservation and Bio-Breeding, No. 130 of Changjiang West Road, 230036 Hefei, Anhui, China
Engineering Research Center of Reproduction and breeding in Sheep of Anhui Province, No. 130 of Changjiang West Road, 230036 Hefei, Anhui, China


  1. Bonneau M, Dufour R, Chouvet C, Roulet C, Squires EJ: The effects of immunization against luteinizing hormone-releasing hormone on performance, sexual development and levels of boar taint-related compounds in intact male pigs. J Anim Sci. 1994, 72: 14-20.PubMedGoogle Scholar
  2. Albrecht A, Beilage EG, Henning M, Bekendorf T, Krieter J: Growth performance and carcass characteristics of Improvac-treated male pigs compared with barrows. Berl Munch Tierarztl Wochenschr. 2012, 125: 456-462.PubMedGoogle Scholar
  3. Kubale V, Batorek N, Skrlep M, Prunier A, Bonneau M, Fazarinc G, Candek-Potokar M: Steroid hormones, boar taint compounds, and reproductive organs in pigs according to the delay between immunocastration and slaughter. Theriogenology. 2013, 79: 69-80. 10.1016/j.theriogenology.2012.09.010.View ArticlePubMedGoogle Scholar
  4. D'Occhio MJ, Aspden WJ, Trigg TE: Sustained testicular atrophy in bulls actively immunized against GnRH: potential to control carcase characteristics. Anim Reprod Sci. 2001, 66: 47-58. 10.1016/S0378-4320(01)00091-4.View ArticlePubMedGoogle Scholar
  5. Brown BW, Mattner PE, Carroll PA, Hoskinson RM, Rigby RD: Immunization of sheep against GnRH early in life: effects on reproductive function and hormones in ewes. J Reprod Fertil. 1995, 103: 131-135. 10.1530/jrf.0.1030131.View ArticlePubMedGoogle Scholar
  6. Brown BW, Mattner PE, Carroll PA, Holland EJ, Paull DR, Hoskinson RM, Rigby RD: Immunization of sheep against GnRH early in life: effects on reproductive function and hormones in rams. J Reprod Fertil. 1994, 101: 15-21. 10.1530/jrf.0.1010015.View ArticlePubMedGoogle Scholar
  7. Clarke IJ, Brown BW, Tran VV, Scott CJ, Fry R, Millar RP, Rao A: Neonatal immunization against gonadotropin-releasing hormone (GnRH) results in diminished GnRH secretion in adulthood. Endocrinology. 1998, 139: 2007-2014. 10.1210/en.139.4.2007.View ArticlePubMedGoogle Scholar
  8. Gökdal O, Atay O, Ulker H, Yarali E, Helva IB, Deavila DM, Reeves JJ: GnRH or eCG treatment fails to restore reproductive function in GnRH immunized ewes. Anim Reprod Sci. 2009, 112: 251-260. 10.1016/j.anireprosci.2008.04.023.View ArticlePubMedGoogle Scholar
  9. Hernandez JA, Zanella EL, Bogden R, de Avila DM, Gaskins CT, Reeves JJ: Reproductive characteristics of grass-fed, luteinizing hormone-releasing hormone-immunocastrated Bos indicus bulls. J Anim Sci. 2005, 83: 2901-2907.PubMedGoogle Scholar
  10. Fang F, Liu Y, Pu Y, Wang L, Wang S, Zhang X: Immunogenicity of recombinant maltose-binding protein (MBP)-gonadotropin releasing hormone I (GnRH-I). Syst Biol Reprod Med. 2010, 56: 478-486. 10.3109/19396368.2010.481005.View ArticlePubMedGoogle Scholar
  11. Fang F, Li H, Liu Y, Zhang Y, Tao Y, Li Y, Cao H, Wang S, Wang L, Zhang X: Active immunization with recombinant GnRH fusion protein in boars reduces both testicular development andmRNA expression levels of GnRH receptor in pituitary. Anim Reprod Sci. 2010, 119: 275-281. 10.1016/j.anireprosci.2010.01.003.View ArticlePubMedGoogle Scholar


© Fang et al.; licensee BioMed Central Ltd. 2013

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