Determination of therapeutic and growth promoting use of clenbuterol by plasma analysis.
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Administration, Oral↗
Biomedical subjects
J C Illera
Publications and source records attributed to J C Illera.
Plasma estradiol-17beta levels and gonadosomatic index in tench (Tinca tinca L.) reared in natural and controlled conditions.
The plasma estradiol-17beta levels (E2-17beta) and gonadosomatic index (GSI) of female tench (Tinca tinca L.) reared outdoors and indoors were studied from December 1996 to April 1997. Water temperature and daylight were gradually increased (from 10 to 25 degrees C and from 9 to 16 hours per day, respectively) in the indoor group. Animals reared in natural conditions had similar plasma levels throughout the experiment but animals under controlled conditions experienced an increase in these levels in March in relation to previous months (4.81+/-0.73 ng/ml in March vs. 0.29+/-0.03 ng/ml and 0.99+/-0.31 ng/ml in January and February, respectively; P < 0.05) and in relation to animals reared outdoors (4.81+/-0.73 ng/ml vs. 0.47+/-0.19 ng/ml, respectively; P < 0.05). In April, a sharp decrease in estradiol-17beta in these animals was observed, probably associated with the end of vitellogenesis. GSI increased in both groups through the experiment and indoor animals showed greater values in March vs outdoor fishes (7.57+/-2.18 vs. 4.05+/-0.63; P < 0.05). No significant correlation was found between E2-17beta and GSI, (r = 0.35). It is concluded that manipulation of the photoperiod and temperature can modify gonadal development in tench, and this is similar to the situation in other Teleostei species. This research is the first step towards achieving, out of season, spawning in tench.
Animals↗
The effect of clenbuterol on adrenal function in rats.
The use of anabolic agents is illegal in the European Community but the effect of these agents on animal welfare is not well documented. The aim of this study was to evaluate whether the administration of anabolic agents, such as clenbuterol, causes stressful effects in rats, as reflected by the adrenal function. Anabolic doses of clenbuterol (1 mg kg-1, 99% purity) were administered orally by stomach tube daily for 45 d to female Long Evans rats (250-300 g, n = 50). Twenty-five animals were used as controls. Blood samples were collected from the jugular vein in anaesthetised animals (ketamine and xylazine). At the end of the experiment, the animals were sacrificed and the adrenal glands were removed. Hormonal levels were measured by an enzyme immunoassay previously validated for this species. Hormonal levels of cortisol and corticosterone, and histopathological analysis, were used as indicators of the adrenal function. Increased corticosterone and cortisol secretion was found in the treated group (p < 0.001), both in adrenal homogenates and peripheral blood samples, compared with control animals. Higher relative adrenal gland weight (adrenal gland-to-body weight ratio) was also found in the treated group (p < 0.01). The major histopathological finding was the presence of hyperplasia in the adrenocortical cells. It was concluded that the administration of an anabolic dose of clenbuterol causes a hyperstimulation of adrenal gland secretion that could adversely affect animal welfare.
Adrenal Glands↗
Effects of HCG or gonadoreline on seminal parameters and plasma testosterone levels in young male rabbits.
The effect of successive HCG or Gonadoreline injections on some reproductive parameters in 21 young male rabbits, aged from 4 to 4.5 months, has been studied. Animals were randomly allocated in three groups of seven to receive weekly (on each Monday) i.m. injections of 20 mg Gonadoreline, 50 IU HCG, or 0.5 ml Saline solution, respectively. The ejaculate from each male was collected and analysed twice a week (Tuesday and Friday). Higher sperm volumes were observed on the first week after Gonadoreline administration compared to the other groups (p < 0.05), and lower values during the second week in the Control group vs. Gonadoreline group (p < 0.05). Sperm volume increases after the 3rd week in Control animals (p < 0.05). When considering the global period studied, mean sperm volumes achieved after Gonadoreline treatment were higher than in HCG or Control group. Despite the random distribution of the animals to each treatment, and although throughout the experiment more ejaculates were discarded in the Gonadoreline group, the final number of doses obtained per ejaculate was higher in this group followed by HCG treated animals. Globally, the mean sperm concentration of the Control group during the entire studied period was significatively lower compared to the other groups (p < 0.001). No sperm motility differences were detected among the groups (p < 0.1174). HCG injections caused a significative increase in plasma testosterone concentration during the first and second week (p < 0.001) and similar plasma levels were observed in all groups afterwards. No direct plasma testosterone increasing levels owed to Gonadoreline injections were detected, probably due to the frequency of blood sampling (once a week).
Animals↗
Developmental competence of immature pig oocytes under the influence of EGF, IGF-I, follicular fluid and gonadotropins during IVM-IVF processes.
Epidermal growth factor (EGF) and insulin like growth factor-I (IGF-I) were evaluated for their effects on in vitro maturation and fertilization in presence or absence of gonadotropin and porcine follicular fluid. Four groups were made with the addition of growth factors: none (control), EGF, IGF-I or EGF+IGF-I. Each group underwent four predefined treatments with gonadotropin (FSH and LH), follicular fluid, a combination of both, or none (as control). Porcine cumulus-oocyte complexes (COCs) were matured in media containing the above-mentioned treatments for 42-44 h prior to fertilization with fresh sperm capacitated for 2.5 h. At the end of the fertilization period, the presumable embryos were fixed, stained and examined as whole-mounts to ascertain their nuclear status. The addition of EGF alone or in combination with IGF-I, significantly increased the proportion of monospermic oocytes forming 2 normal pronuclei. Also, supplementation with both growth factors together enhanced the percentages of pronucleus formation and total penetration. In addition, treatments with EGF+IGF-I significantly decreased (P<0.01) the incidence of degeneration in fertilized oocytes. However, no significant differences in the proportions of COCs undergoing polyspermy were observed among all treatments. These results suggest a stimulatory effect of tested growth factors in maturation and fertilization of pig oocytes. Furthermore, gonadotropins and follicular fluid can be replaced by the addition of EGF and IGF-I to the maturation media with positive effects on fertilization rate.
Animals↗
Steroid-level response to insulin-like growth factor-1 in oocytes matured in vitro.
The objective was to establish the influence of insulin-like growth factor-1 (IGF-1) on steroid production and nuclear maturation during oocyte in vitro maturation (IVM). Immature-selected rabbit follicular oocytes, divided as cumulus-oocyte complexes (COC) and denuded oocytes (DO), were cultured in Brackett's medium with different concentrations of IGF-1 at 0, 50, 100 and 200 ng/ml. After 8 and 16 h of culture, the oocytes were assessed for nuclear maturation by acetic-orcein stain, and media were analyzed by enzyme-immunoassay (EIA) for 17 beta-estradiol (E), progesterone (P), androstenedione (A) and testosterone (T) content. After culture treatments with IGF-1 significantly increased (P < 0.01) the incidence of nuclear activation (germinal vesicle breakdown stage, GVBD) and nuclear maturation (metaphase II stage); maximum stimulation occurred at 100 ng IGF-1/ml (86.9 vs. 49.3% in control). Compared to controls, the presence of IGF-1 in cultures was associated with a significant increase of E and A production by COCs (P < 0.01). However, P and T levels were not significantly influenced by the IGF-1. In addition, positive correlations between E/T and E/A ratios and nuclear maturation rates were only found in the IGF-1 treatments. Regarding the DOs, neither positive effects in nuclear maturation rates nor increase of steroid levels in culture were observed for any treatment. These results suggest that: (1) IGF-1 had a significant effect on E and A production during oocyte maturation; (2) the addition of IGF-1 enhanced nuclear maturation significantly in rabbit oocytes; and (3) all these effects are only possible in oocytes surrounded by cumulus cells.
Androstenedione↗
ELISA for the measurement of serum and urinary chorionic gonadotropin concentrations in the laboratory macaque.
A rapid, sensitive, enzyme-linked immunosorbant assay (ELISA) for the measurement of chorionic gonadotropin (CG) in serum and urine samples of laboratory macaques is reported. The ligand (CG) is captured by a readily available, widely used, and well-characterized monoclonal antibody (Mab, 518B7) generated against the beta subunit of bovine luteinizing hormone (LH). This Mab, while specific for LH, shows very little species specificity, and has been shown to detect LH and CG by radioimmunoassay (RIA) in both human and non-human primates. A polyclonal antiserum raised in rabbits against human chorionic gonadotropin (hCG) is conjugated to horseradish peroxidase, and is used as the second antibody signal. This anti-hCG antiserum cross reacts with CG secreted by both the human (hCG) and macaque (mCG). The ELISA utilizes hCG as the standard, and results are based on the relative concentrations of mCG in serum and urine. Total assay time is less than 5 hours. Range of the standard curve is 0.002 to 0.5 ng hCG/well, and the least detectable concentration of hCG is 0.0023 +/- 0.0007 ng/well. Pregnancy was detected in early pregnant macaques (M. fascicularis) on 9 (N = 1/16), 10 (N = 1/16), 11 (N = 1/16), 12 (N = 6/16), 13 (N = 1/16), 14 (N = 4/16), and 15 (N = 2/16) days following the pre-ovulatory urinary estrone conjugate peak. The detection of pregnancy by urinary mCG occurred approximately 24 to 72 hours after its detection in serum.
Animals↗
Enzyme immunoassay for testosterone and androstenedione in culture medium from rabbit oocytes matured in vitro.
Two enzyme immunoassays (EIAs) were validated to determine testosterone and androstenedione levels in culture medium (Brackett's medium with or without the addition of IGF-I, hormone and serum-free), without previous extraction, from rabbit oocytes matured in vitro. Polyclonal testosterone (C917), and androstenedione (C9111) antibodies were raised in rabbits using testosterone 3-carboxymethyloxime:BSA, and androstenedione 3-carboxymethyloxime:BSA. Horseradish peroxidase was used as label, conjugated to testosterone 3-carboxymethyloxime, and to androstenedione 6-hemisuccinate. Standard dose response curves covered a range between 0 and 1 ng/well. The low detection limits of the technique were 11.43 pg/ml for testosterone, and 2.32 pg/ml for androstenedione. Intra- and inter-assay coefficient of variation percentages were < 6.4 and < 7.1 for testosterone, and < 5.1 and < 6.3 for androstenedione, respectively (n= 10). The recovery rate of known testosterone or androstenedione concentrations added to pools of culture maturation medium samples averaged 97.58 +/- 2.11%, and 95.73 +/- 1.59%, respectively. Compared with RIA, EIA values were in close agreement for testosterone (n= 15, r= 0.96, P< 0.001), and androstenedione (n= 15, r= 0.94, P< 0.001). Culture medium samples were obtained at the end of oocyte in vitro maturation (14-16 h). Mean +/- SE culture maturation medium concentrations (ng/ml) were 1.80 +/- 0.09 and 0.52 +/- 0.01 for testosterone, and 1.70 +/- 0.04 and 0.24 +/- 0.01 for androstenedione in both the oocytes with and without cumulus cells, respectively. We concluded that our EIA is a highly sensitive and specific assay that provides a rapid, simple, inexpensive and nonradiometric alternative to RIA for determining testosterone and androstenedione concentrations in oocyte maturation culture medium.
Journal Article↗
Effect of gonadoreline and naloxone on induction of ovulation and plasma LH in rabbit.
To study the effect of an opiate antagonist receptor (naloxone) on LH secretion, two groups of seven does were randomly allocated to GnRH (gonadoreline, 20 microgram/animal), and GnRH + naloxone (1.8 mg/kg b.w.) treatment, respectively and another group of eight animals was treated with naloxone alone. Blood samples were obtained immediately before treatment (0 minutes) and at 60, 120 and 180 minutes after injection. Plasma levels of LH were determined by a direct, simple and precise sandwich enzyme immunoassay (EIA), adapted for measuring plasma LH in rabbit. Luteinizing hormone reached maximum values 60 minutes after administration of GnRH or GnRH + naloxone (p < 0.05) and all the females of these groups ovulated. Only 25% of naloxone treated rabbit does ovulated and these animals presented a high LH plasma level at 60 minutes post-treatment (p < 0.05). In non ovulated animals no variations in plasma LH concentrations were observed at 60 minutes, in relation to blood samples obtained at 0, 120 and 180 minutes. Results show a limited effect of this naloxone dose on the anterior pituitary of non lactating adult rabbi does in relation to induced ovulation. No synergic effect was detected when naloxone was administered in addition to gonadoreline.
Animals↗
A sensitive EIA for 17 beta-estradiol and progesterone in culture medium for oocyte in vitro maturation procedures.
A sensitive heterologous enzyme immunoassay (EIA) was validated to determine 17 beta-estradiol (E2) and progesterone levels, without previous extraction, in culture medium from rabbit oocytes matured in vitro with and without the addition of IGF-I. Polyclonal E2 (C902), and progesterone (C914) antibodies were raised in rabbits using 6-keto-17 beta-estradiol 6-carboxymethyloxime:BSA, and 11 alpha-hydroxyprogesterone 11 alpha-hemisuccinate:BSA. Horseradish peroxidase was used as label, conjugated to 17 beta-estradiol 3-hemisuccinate, and to progesterone 3-carboxymethyloxime. Standard dose response curves covered a range between 0 and 1 ng/well (100 microliters). The low detection limits of the technique were 1.99 pg/well for E2, and 13.21 pg/well for progesterone. Intra- and interassay coefficient of variation percentage (% CV) were < 6.3 and < 7.8 for E2 and progesterone, respectively (n = 10). The recovery rate of known E2 or progesterone concentrations added to a pool of culture maturation medium averaged 96.39%, and 98.65%, respectively. Compared with RIA, EIA values were in close agreement for E2 (n = 15, R = 0.96, P < 0.001), and progesterone (n = 15, R = 0.99, P < 0.001). Medium samples were obtained after oocyte maturation in vitro for 16 h. Use of IGF-I significantly elevated steroids production in the oocyte surrounded cumulus cells. The EIA described here is highly sensitive and specific assay, and provides a rapid, simple, inexpensive, and non-radiometric alternative to RIA for determining E2 and progesterone levels in oocyte culture medium.
Animals↗
Stimulatory effect of insulin-like growth factor I and epidermal growth factor on the maturation of rabbit oocytes in vitro.
The effects of different combinations of epidermal growth factor (EGF) and insulin-like growth factor I (IGF-I) on cumulus expansion and meiotic maturation were examined in rabbit oocytes. Selected rabbit follicular oocytes were matured in vitro and were classified as cumulus-oocyte complexes or denuded oocytes. They were cultured in TCM 199, and were treated with growth factors at different concentrations: EGF at 0, 1, 10, 50 and 100 ng ml-1, IGF-I at 0, 50, 100 and 200 ng ml-1 and EGF plus IGF-I at 10 + 50; 10 + 100; 50 + 50 and 50 + 100 ng ml-1, respectively. After 6 h of culture, the oocytes were assessed for nuclear maturation and after 16 h of culture, for cumulus expansion and maturation stage. After culture for 6 h, the incidence of germinal vesicle breakdown was higher (P < 0.05) in all of the growth factor treatments tested compared with controls. After culture for 16 h, EGF enhanced the incidence of cumulus expansion at all of the concentrations tested. Cumulus expansion was greatest with 50 mg EGF ml-1 plus 100 ng IGF-I ml-1 (72.0% versus 2.4% in controls). Treatment with IGF-I significantly increased (P < 0.05) the incidence of metaphase II stage, and maximum stimulation occurred at 100 ng IGF-I ml-1 (84.5% versus 31.1% in controls). However, IGF-I did not affect cumulus expansion. When denuded oocytes were used, no positive effects on nuclear maturation rates were observed for any treatment. These results suggest that: (1) EGF, either alone or with IGF-I, stimulates cumulus expansion; (2) the addition of IGF-I or EGF plus IGF-I significantly enhances nuclear maturation in immature rabbit oocytes; and (3) this effect is mediated by the presence of cumulus cells.
Animals↗
Development of a simple, rapid sandwich enzyme immunoassay for the measurement of serum rat LH.
The present study describes the development and validation of a rapid, sensitive, specific and precise enzyme immunoassay (EIA) sandwich suitable for measuring luteinizing hormone (LH) in rat serum. Ninety-six well polystyrene microtiter plates were coated with 100 microliters (250 ng/ml) of a well-characterized monoclonal antibody (518B7, Roser, UC Davis) generated against bovine LH. A polyclonal antiserum raised in rabbits against ovine FSH (G4-215B, Papkoff) was conjugated to sodium periodate-activated horseradish peroxidase (HRP), and used as the second antibody of the sandwich assay. This anti-ovine FSH antiserum cross-reacted more than 200% with rat LH. Standards (r-LH-RP-3, NIADDK, range 0 pg/well to 2.5 ng/well or 100 microliters) diluted in a 3(N-Morpholino) propane sulfonic acid (MOPS) buffer, or serum, were incubated with the solid phase antibody for 2 hours. Plates were washed and the anti-oFSH:HRP (100 microliters) in MOPS buffer was added and incubated a further 2 hours before a second wash and the addition of the substrate (TMB, 3,3',5,5'-tetramethylbenzidine dihydrochloride and H2O2). The least detectable concentration of LH was 16.1 +/- 1.42 pg/ml. The recovery of known concentrations of LH added to several samples was 93.5 +/- 1.70%. Mean intra-assay and inter-assay coefficients of variation (%) were less than 10% (n = 20). The anti-FSH:HRP showed less than 8.0% cross reactivity with rFSH in this LH EIA system. The correlation coefficient (r) of samples analyzed by EIA in parallel with RIA was r = 0.90 (p < 0.001, n = 26). Results showed levels between 105.21 and 633.87 pg/ml. This new LH EIA sandwich offers a stable, rapid, and improved EIA system for the measurement of serum LH concentrations of this species over previously reported methods.
Animals↗
[Chronological aspects of the nuclear maturation of bovine oocytes cultivated in vitro].
In this study, the chronological changes in the meiotic progress of in vitro maturation of bovine oocytes was analysed. Oocytes (n = 1044) were obtained from a local abattoir and were classified into two groups according to the presence or absence of cumulus cells. They were incubated in microdrops (5 per drop) in TCM-199 (control), TCM-199 + 10% fetal calf serum (treatment 2) and TCM-199 + 10% estrous cow serum (treatment 3). Oocytes were fixed and stained at the end of 0, 6, 12, 18, 24 and 30 h of the beginning of in vitro culture, were evaluated according to the nuclear stage of maturation. These results demonstrated that the immature oocytes at the time of collection (0 h) were in the germinal vesicle stage (GV), and that the highest maturation rate was at 24 h of culture in all treatments. Serum treatments enhanced the maturation rates obtained (52.1 and 55.7%) compared to control (serum-free) medium (42.7%; P < 0.05) in cumulus-cell-enclosed oocytes. In denuded oocytes, the maturation rates were lower compared to cumulus-cells-enclosed oocytes in all treatments. In conclusion, meiotic progression of bovine oocytes can be influenced by the inclusion of sera in the maturation media and by the presence of the cumulus cells.
Animals↗
Circadian rhythms of the salivary proliferation markers CA130 and CA125 in clinical health.
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Adult↗
Influence of growth factors on the time-dependent meiotic progression of the bovine oocytes during their in vitro maturation.
The present study examines the effects of epidermal growth factor (EGF), insulin-like growth factor-I (IGF-I), and the presence of cumulus cells on the meiotic progression of the bovine oocyte maturation. Oocytes were aspirated from 2-8 mm ovarian follicles, and the cumulus-oocyte complexes (COC) obtained (n = 2,729) were divided into COC or denuded oocytes. They were then cultured in four defined treatments comprising TCM-199 and growth-factors: control (no growth factor), IGF-I, EGF, and EGF+IGF-I. Each treatment group of oocytes was cultured during 6, 12, 18, 24, and 30 h; the oocytes were fixed and stained at the end of each 6 hour interval from 0 to 30-h, and were assessed for their nuclear maturation stage. Germinal vesicle (GV) and metaphase II (MII) stages present were used as the final parameters for data analysis. The results indicate that treatments with growth factors enhanced the incidence of GV activation and MII stage in all the culture periods. Maximal stimulation for nuclear maturation occurred with EGF+IGF-I. As regards the denuded oocytes, no positive effects on nuclear maturation rates were observed for any treatment. These results suggest that EGF and IGF-I, singly and combined, stimulate the meiotic progression significantly, and this effect can be induced by a positive signal which is transferred from cumulus cells to oocyte.
Animals↗
Enhancement of cumulus expansion and nuclear maturation during bovine oocyte maturation in vitro by the addition of epidermal growth factor and insulin-like growth factor I.
This study was carried out to identify the possible effects of epidermal growth factor (EGF) and insulin-like growth factor-I (IGF-I) on cumulus expansion and nuclear maturation in bovine oocytes matured in vitro in serum-free media. Bovine follicular oocytes were matured in vitro and were then classified as cumulus cell-enclosed oocytes or denuded oocytes. They were then cultured for 24 h in TCM-199 (tissue culture medium-199) with EGF (50 ng ml-1), IGF-I (100 ng ml-1) and EGF plus IGF-I (50 and 100 ng ml-1, respectively). At the end of the culture period, the morphology of oocytes was evaluated for cumulus expansion and nuclear stage of maturation. In Expt 1, percentages of oocytes reaching maximum cumulus expansion were: 12.5% (control), 46.5% (EGF), 15.2% (IGF-I) and 52.8% (EGF plus IGF-I). In Expt 2, the respective rates of nuclear maturation were: 35.6%, 52.1%, 45.5% and 61.4% for cumulus cell-enclosed oocytes, and 35.3%, 46.6%, 45.4% and 42.5% for denuded oocytes; the same growth factor treatments were used in both cases. There was no significant effect of IGF-I on cumulus expansion. Maximum rates of cumulus expansion and nuclear maturation were obtained in the presence of both growth factors. These results lead to the following conclusions: (i) EGF, either alone or together with IGF-I, stimulates cumulus expansion; and (ii) both growth factors, acting alone or together, enhance nuclear maturation in oocytes surrounded by compact cumulus cells.
Animals↗
Determination of follicular fluid estradiol levels by enzyme-linked immunosorbent assay.
A direct competitive heterologous enzyme-linked immunosorbent assay (ELISA) was developed and validated to determine follicular fluid estradiol levels of different antral follicular sizes (small, medium, and large) obtained from the ovaries of heifers in the follicular phase of the estrous cycle. Polyclonal antiestradiol antibodies were raised in New Zealand White rabbits using 6-keto-1,3,5(10)-estratriene-3,17 beta-diol 6-carboxymethyloxime: bovine serum albumin as immunogen and characterized by the usual methods. Horseradish peroxidase conjugated to 1,3,5(10)-estratriene-3,17 beta-diol 3-hemisuccinate was used as a label. The concentration range used for the standard curve was 0 to 1 ng per well. The low detection limit of the technique was 0.3 pg per well with a sensitivity at 50% binding of 93.62 pg per well. Intraassay and interassay CV (%) were < 5.3% and < 7.0%, respectively (n = 10). The recovery rate of the known estradiol concentrations added to follicular fluid averaged 96.1 +/- 1.3%. Compared with a radioimmunoassay (RIA), the values of ELISA were highly correlated (r = 0.99, P < 0.005). This assay was used to quantify follicular fluid estradiol concentrations without previous extraction in three antral follicular sizes; small (< 5 mm), medium (5.1 to 10 mm), and large (10.1 to 20 mm). The mean +/- SE follicular fluid estradiol concentrations were 77 +/- 5.2 ng/ml (n = 490) in small follicles, 111 +/- 19 ng/ml (n = 65) in medium follicles, and 496 +/- 144 ng/ml (n = 45) in large follicles.(ABSTRACT TRUNCATED AT 250 WORDS)
Animals↗
Development and validation of competitive ELISA to determine follicular fluid progesterone concentrations.
A simple, direct and reliable heterologous ELISA was developed and validated to determine follicular fluid progesterone concentrations in 10- to 20-mm antral follicles in heifers. A competitive ELISA was developed, using a policlonal antisera raised in New Zealand white rabbits and horseradish peroxidase as label. Standard curve covered a range between 0 and 1 ng per well. The intra- and inter-assay coefficients of variation (CV) were 6.54 and 8.27%, respectively (n = 10). The low detection limit was 1 pg per well with a sensitivity of 50% binding 83.17 pg per well. Comparison of ELISA with RIA showed a correlation coefficient of 0.98. A total of 34 follicles obtained from heifers in the follicular phase of the estrous cycle were tested, and the mean progesterone concentration was 86.72 +/- 20.39 ng/ml. These results were similar to those previously reported for the same species, age, follicular size and stage of cycle.
Journal Article↗