Background
Stress is a well-known factor influencing reproductive performance in animals [
1] Stressors come in various forms, and events such as weaning, grouping, and transportation have all been shown to influence reproduction in pigs and the pigs’ response to each of these stressors is different [
2]. Responses to stress vary in response to factors such as type of stressor, duration, intensity, and individual variation between pigs [
1‐
3]. It is difficult to compare and evaluate the different stressors that affect pig reproduction, particularly in long-term situations. A previous study found that ovarian cysts are an important disorder for sows, which accounted for 10% of reproductive problems in pigs [
4]. However, little is known about ovarian cysts, because it may happen without the performance of reproduction confusion [
4]. Although it is difficult to diagnose ovarian cysts, it is established that endocrine disruption is associated with ovarian cysts [
5]. The confusion of endocrinological mechanisms plays a role in infertility by altering the physiology of gonadal tissues [
5]. Stress results in alterations in hormonal events along with the immediate endocrine; some studies have reported that endocrine imbalance is the primary reason for the occurrence of ovarian cysts [
6,
7]. Although stress-inducing practices such as sow crating and tethering have been gradually replaced by group penning to improve animal welfare, group penning can also give rise to stress among pigs due to animals pushing, riding, and biting one another [
8]. Thus, stress is inevitable and difficult to evaluate. In pig production, many events can potentially cause stress and it is difficult to assess the precise relationship between stress and reproduction due to the varied number and type of stressors.
A series of studies have shown that reproduction in pigs is always impaired by stress through the neuroendocrine system [
1,
9‐
11]. Without exception, various types of stress can activate the hypothalamic-pituitary-adrenal (HPA) axis, affecting hormone release and ovarian function [
12]. Activation of the HPA axis suppresses gonadotropin secretion and influences ovarian activity by increasing the production of glucocorticoids [
12]. The HPA axis is activated in response to stress, triggering the release of corticotrophin-releasing hormone (CRH) and vasopressin by the hypothalamus. Increased levels of CRH lead to increased ACTH release from the anterior lobe of the pituitary [
2,
5]. ACTH acts on the adrenal cortex, stimulating the release of glucocorticoid hormones (e.g., cortisol in pigs) and influencing the physiological state of the sexual organs and steroid hormone pathways [
13]. Exogenous ACTH administration has been shown to affect not only the adrenal glands but also the reproductive organs and several hormonal pathways either directly or by alterations in the cortisol level [
14]. At ovulation, increased estradiol-17β (E
2) and decreased progesterone (P
4) concentrations in the plasma lead to increase in the frequency of GnRH secretion, contributing to the preovulatory LH surge [
10]. Steroid hormones play a role in ovarian structures remote from the luteal or follicular cells where they are produced, and the process is realized by endocrine mechanisms [
5,
15]. Decrease in the levels of steroid hormone can influence follicular development and even ovulation [
16‐
18]. In general, androgens are secreted in granulosa cells and converted to E
2 by P450arom; androgen levels are higher when the expression of the aromatase is suppressed, and this contributes to the formation of ovarian cysts [
19]. Increased plasma cortisol levels lead to a decrease in the expression of steroidogenic enzymes and impair the synthesis capacity of E
2 [
20]. When the plasma E
2 concentration is reduced, the positive feedback effect on GnRH/LH secretion is weakened and the preovulatory LH surge is then suppressed, ultimately affecting the success of ovulation [
21].
ACTH administration did not significantly alter the plasma E
2 and LH concentrations compared to the control group [
13]. A review reported that no significant differences were found in the LH levels between control animals and experimental animals injected with ACTH, but the interval of the LH peak to ovulation showed a significant difference. The time from LH peak to ovulation was longer in the ACTH group than in the control group [
12]. LH functions by binding to its receptors, and the LHR is the primary medium by which LH affects follicle development and maturation by stimulating the synthesis and secretion of steroid hormones [
22].
Therefore, we aimed to study the effect of ACTH injection on the development and function of ovarian follicles; androstenedione levels; progesterone and E2 levels in follicular fluid (FF); LH receptor expression; and the expression of steroidogenic enzymes such as P450scc, P450c17, P450arom, StAR, and 3β-hydroxysteroid dehydrogenase (3β-HSD) in granulosa and theca cells of the ovarian follicle. To this end, we induced long-term stress in weaned sows by ACTH administration for 7 days.
Experimental design
Grouping and jugular vein catheter
The jugular vein was cannulated on the weaning day and defined as day 1 of the experiment. Sows were fixed to a test bench after they were sedated with thiopentone sodium. A cannula was passed into the exposed jugular vein, while the free end of the cannula was passed subcutaneously and fixed behind the ear with adhesive bandage. After the surgery, the sows were randomly divided into two groups: an ACTH group and a control group (n = 5 per group). From days 2–8 after the surgery, animals in the ACTH group received 1 IU ACTH/kg body weight every 8 h. The ACTH was obtained from porcine pituitary glands (A6303, Sigma, USA). Sows in the control group received the same dosage of saline (0.09%) on the same schedule as the ACTH group. The cannula was filled with heparinized saline (0.09%) to prevent coagulation.
Blood sampling
Blood samples were collected every 3 h starting from 9:00 am on day 2 until pro-estrus. After the start of estrus, blood samples were then collected every 1 h. The blood samples (10 mL) were collected into a heparinized vacuum blood tubes, centrifuged for 10 min at 1000 g, and stored at −20 °C until analysis.
Collections of FF and follicle tissues
Porcine ovaries were collected within 10 min of slaughter of weaned sows. Follicles were then stripped from the ovary using sterile scissors and placed on ice. FF without blood was collected from each single follicle, and then stored at −80 °C for P4, E2, and androstendione (ASD) assays. Meanwhile, follicular tissues were stripped from the follicles using sterile scissors, and the tissues were then stored at −80 °C for extraction and analysis of mRNA.
Detection of cortisol, P4, E2, and ASD levels in FF
The P4, E2, and ASD levels in follicular fluid were determined by ELISA assay kits (H089 and H102, Jiancheng, Nanjing, China; and 33–33720, TIANDZ, Beijing, China respectively) and the plasma cortisol level was evaluated by the same method (ANG-E31032P, Aoqing, Nanjing, China). All FF and plasma samples were centrifuged at 3000 rpm for 20 min at 4 °C. After centrifugation, all samples were diluted 1:5 in sample diluents and detected at 450 nm using a multimode reader (Infinite 200 PRO; Tecan, Geneva, Switzerland). The E2:P4 ratio was calculated after the E2 and P4 levels were detected in follicular fluid.
Fluorescence quantitative real-time PCR
Total RNA was isolated using TRIzol reagent (Trizol-RNAiso Plus reagent, D9108A, Takara, China), and reverse transcription was carried out using Transcript Moloney murine leukemia virus kit (Invitrogen, Shanghai, China). For total RNA collection, 100 mg of follicle tissue was homogenized with 1 mL RNA extraction buffer (TRIzol; Takara Biotechnology, co., Ltd.) in a Super Fine Homogenizer (623003, Fluko, Germany). Once the total RNA was extracted, its concentration was determined by measuring absorbance in a spectrophotometer (M200PRO; Tecan, Austria) at 260 nm. The sequences of the
lhr, star, p450scc, p450arom, p450c17, 3β-hsd were obtained from the National Center for Biotechnology Information Genbank. Table
1 presents the sequences and sizes of the
lhr, star, p450scc, p450arom, p450c17, and
3β-hsd genes.
Table 1
Sequences and sizes of all tested genes
LHR
| NM-214449.1 | sense GCTCACCCAAGACACTCC | 190 |
antisense CACATGAGGAAACGAGGC |
StAR
| NM-213755.2 | sense GGCAAGGCTCTTCTAACT | 99 |
antisense TAGACACGAAAGGGCTCA |
P450scc
| NM-214427.11 | sense CCAGCATTACCAGAAGCC | 92 |
antisense GAGCCATTACCTCCGTGT |
P450arom
| NM-214429.1 | sense AAGAAGGGTCACAACAAG | 165 |
antisense AAGAAAGCCAGTGAGCAG |
P450c17
| NM-214428.1 | sense ATGATCCAAGCCAAGACG | 140 |
antisense TTTACCACAGAGGCAGAAG |
3β-HSD
| NM-001004049.1 | sense CCTGGCAAGTATTTCTCGG | 107 |
antisense CCAGCAACAAGTGGACGAT |
β-actin
| NM-001167795.1 | sense CTCCATCATGAAGTGCGACGT | 114 |
antisense GTGATCTCCTTCTGCATCCTGTC |
Immunohistochemical staining
Ovaries of the tested sows were obtained within 10 min of slaughter. They were then fixed in 4% formalin solution buffer (pH 7.4) for 24 h, and embedded in paraffin. Serial 5-μm-thick sections of ovarian follicles were cut and the sections were mounted onto 3-aminopropyltriethoxysilane (APES)-coated slides.
Sections were deparaffinized in xylene and dehydrated in an ascending ethanol series, and washed three times in PBS for 3 min each time. Antigen retrieval was carried out in 0.01 M sodium citrate buffer (pH 6.0) in a microwave oven, and the sections were rinsed three times with PBS for 3 min each time. The sections were then immersed in 3% hydrogen peroxide for 10 min to inactivate the endogenous peroxidase at room temperature. After inactivation, antigen retrieval was carried out in a microwave oven and nonspecific binding was blocked with 5% BSA. The following primary antibodies were used: anti-CYP19A1 (1:100, A1336, ABclonal Technology, Wuhan, China), anti-CYP17A1 (1:100, A1373, ABclonal Technology, Wuhan, China), anti-3βHSD (1:100, sc-30820, Santa Cruz Biotechnology, CA, USA), and anti-LHR (1:100, K-15, Santa Cruz Biotechnology, CA, USA). For the negative controls, 1% bovine serum albumin was used instead of the primary antibody. Next, sections were incubated with horseradish peroxidase (HRP)-conjugated goat anti-rabbit lgG (H + L; 1:150 dilution, IH-0011; Dingguo, Beijing, China) for 1 h at 37 °C. The reactions were visualized by treatment with diaminobenzidine (DAB) (AR1022, Boster, Wuhan, China) for 15 s.
Image-Pro Plus 6.0 software was used to evaluate the staining intensity by the average optical density (AOD). Ten typical fields were selected to estimate the percentage of immunopositive cells, and each field was examined twice by three authors.
Statistical analysis
Data of the ACTH and control groups were analyzed by independent sample t test using Statistical Package for Social Science software (SPSS version 20.0 for Windows). All data are represented as the mean ± standard deviation (SD) and a P value of <0.05 was considered statistically significant.
Discussion
Although it is commonly known that stress induces disorders in follicular development and ovulation, the underlying mechanism remains unclear. ACTH administration has been reported to simulate the stress response, which is reflected by the plasma cortisol response, and influenced reproduction in pigs [
8,
9,
11,
13,
23,
24]. In the present study, we administered sows with repeated ACTH injections to mimic stress; this resulted in an increase in the plasma cortisol concentration in the sows that were treated with ACTH but not in the untreated control sows, indicating successful establishment of a stress model. Previous studies mainly focus on the changes in the hormone levels in plasma, but hormone levels were not obviously affected by ACTH administration [
8,
13]. Therefore, in our study we investigated changes in the steroid hormone levels in follicular fluid and LHR expression in the ovarian follicular wall in the stress model.
Cortisol is a sensitive indicator of stress, and our study found that sows with ACTH-induced stress had much higher plasma cortisol concentrations than control sows; our findings are in agreement with those reported previously [
2,
25]. In addition to the higher plasma cortisol concentration, sows in the ACTH group also showed reduced E
2 and ASD levels in FF and lower E
2/P
4 ratio compared to the corresponding values in the control group. Interestingly, the P
4 concentration in FF did not significantly differ between the two groups. Ovarian steroidogenesis is known to be a multistep process involving many key enzymes [
26]. The above results indicate that ACTH may not significantly affect the transcription of certain key enzymes. Cortisol, which is released by adrenal glands due to exogenous ACTH, is capable of damaging ovarian function [
2,
27,
28]. ACTH, which is secreted from the pituitary gland, can induce cortisol secretion by acting on the adrenal gland [
10,
25]. Increase in the plasma cortisol concentration would initiate the negative feedback of E
2, which would then suppress the frequency or amplitude of GnRH, reducing the secretion of gonadotrophin [
28]. At the hypothalamo-pituitary level, gonadotrophin inhibition influences ovulation and triggers the formation of small ovarian cysts [
24,
29]. Hormonal interaction of the HPA and hypothalamic-pituitary-gonadal (HPG) axes contributes to reproductive problems in female pigs [
5]. Increased cortisol concentrations can suppress the synthesis of steroid hormones and can even impair the preovulatory LH surge, resulting in ovulation failure [
27,
28]. Suppression of the LH surge can impair follicle development and estrogen synthesis as well as increase the formation of follicular atresia [
17]. Steroid hormone release is controlled by endocrine mechanisms, and changes in the concentrations of steroid hormones will influence reproductive function [
5]. Steroid hormones are important factors affecting ovarian follicle growth and ovulation in weaning sows. As paracrine/autocrine agents, these hormones can play roles on or within the cells where they were produced [
15].
Ovarian steroidogenesis is a multistep process involving several key enzymes [
26]. Enhanced E
2 biosynthesis ability is always accompanied by upregulation of LHR and some steroidogenic genes [
30]. In the present study, the follicular fluid of the ACTH group had reduced E
2 and ASD concentrations. Accordingly, the
lhr,
3β-hsd, cyp19a1, and
cyp17a1 mRNA levels were also reduced in the ACTH group compared to the control group; this reduction may be associated with the high plasma cortisol levels induced by ACTH. The frequency or amplitude of GnRH could be suppressed with the increased in the plasma cortisol level [
28]. In addition, treatment with a GnRH receptor antagonist has been shown to decrease LH secretion and reduce the
lhr,
cyp19a1, and
cyp17a1 mRNA levels [
31]. Compared to the control group, the ACTH group had a lower E
2/P
4 ratio, and the
lhr,
cyp19a1, and
cyp17a1 levels were lower in estrogen-inactive follicles than in estrogen-active follicles [
32]. The mRNA and protein levels of these enzymes were related to the biosynthesis and transfer of androgens. In previous literature, 3β-HSD was shown to convert pregnenolone into P
4 and transfer this hormone outside the mitochondria, while P450c17 was shown to produce ASD via 17-hydroxylation of P
4 [
33]. The results of the immunohistochemical staining in our study revealed positive signals of P450c17 and 3β-HSD distributed in theca cells, and these positive signals were reduced in the ACTH group compared to the control group. When the 3β-HSD expression level is reduced, it interferes with the ability of P
4 transfer, resulting in ASD biosynthesis and reduced P
4 concentration. Similarly, the suppression of P450c17 reduces the 17-hydroxylation activity of this enzyme, consequently affecting ASD biosynthesis [
18]. Except for aromatization, which occurs in granulosa cells, all other processes of steroidogenesis occur in theca cells. P450arom is expressed in granulosa cells and is the last key enzyme that plays a role in the formation of estrogens from androgens [
34]. Disruption of ovarian steroid synthesis in sows may be associated with defects in the aromatase complex, which influences hormone conversion in peripheral fat tissue [
10]. Suppression of P450arom activity can reduce the E
2 concentration in FF [
35,
36]. In a study on women with polycystic ovary syndrome (PCOS), the P450arom expression levels in granulosa cells were very low and undetectable, indicating that the process of conversion of androgens into estrogens was disturbed, affecting the development of the ovarian follicle [
37].
Estrogens can regulate the development of ovarian follicles by stimulating the proliferation of granulosa cells [
38]. Decrease in the estrogen levels could influence the LH surge [
39] and the LHR expression in the ovary [
22]. LHR expression is a vital mediator for the various functions of LH in sows, in including ovulation. LH can influence the P
4 and ASD production and induce ovulation by binding to the LH receptor [
40]. A previous study reported that inactivation of LHR by gene mutation affected follicular development at all stages [
41]. Glucocorticoids have been shown to influence the responsiveness of gonadal to LH and the expressions of LHR [
42]. LHR production increases with follicle development and matures before ovulation [
43] while the expression would be influenced by many elements such as the circulating LH levels [
31]. The cortisol that is produced in response to stress suppresses GnRH secretion and decreases the LH level [
28]. The ACTH-induced increase in the plasma cortisol level affects the LHR expression in ovarian follicular walls. In addition, LHR expression is related to estrogen activity, and LHR expression has been found to be lower in estrogen-inactive follicles than in estrogen-active follicles [
32].