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1.
The effects of an intraperitoneal hormone injection of gonadotropin‐releasing hormone agonist (D‐Ala6, Pro9‐NEt GnRHa) alone or in combination with a dopamine antagonist, domperidone (DOM), on ovulation induction in yellow catfish Pelteobagrus fulvidraco were tested. The hormone treatments were as follows: 6 mg kg−1 body weight (BW) of carp pituitary extract as a positive control, GnRHa 10, 20, 40 and 80 μg kg−1 BW and a combination of GnRHa and DOM as follows: 10 μg+5 mg, 20 μg+10 mg, 40 μg+20 mg and 80 μg+40 mg kg−1 BW. Physiological saline (0.7% NaCl) was used as a negative control. Significant differences in the ovulation ratio, latency period and ovulation index (OI) were observed among treatments (P<0.05). The combination of GnRHa and DOM at doses of 40 μg+20 mg kg−1 BW had higher values of the ovulation ratio and OI, and a shorter latency period compared with other treatments. The highest OI in GnRHa treatments was only 56.67%, suggesting a dopaminergic tone on gonadotropin secretion in this fish at the pre‐ovulatory stage. Therefore, ovulation can be successfully induced in yellow catfish with 40 μg kg−1 GnRHa+20 mg kg−1 DOM without affecting the egg quality.  相似文献   

2.
The effects of a single injection of mammalian superactive analogue [d ‐Ser(tBu)6,Pro9‐NEt]‐LHRHa (20 μg/ kg?1) combined with the dopamine antagonist, haloperidol (HAL, 0.5 mg kg?1), for induction of ovulation in the koi carp broodstocks were determined under routine hatchery conditions. The results were compared with classic carp pituitary extract (CPE, double injection) application (water temperature 22 °C). Physiological saline (0.7% NaCl)‐injected fish were used as a control group and no ovulation occurred in this group. The spawning ratio was high in the LHRHa+HAL treatment group and in the CPE treatment group (6/7 and 5/7 respectively). The latency period was 14–16 h in the LHRHa+HAL treatment group and 12–14 h in the CPE treatment group (after the second injection). There was no difference between the two ovulating groups with respect to the spawning index (the weight of eggs as a percentage of female body weight) and fertilization rate of eggs (P>0.05). As a result, ovulation can be induced successfully in koi carp broodstocks with 20 μg kg?1 [d ‐Ser(tBu)6,Pro9‐NEt]‐LHRHa+0.5 mg kg?1 HAL treatment in a single injection without decreasing the egg quality. Application of this combination can be useful for hatchery and broodstock management in koi carp culture.  相似文献   

3.
To induce synchronized ovulation, migrating wild Caspian brown trout (Salmo trutta caspius) females were treated with two interperitoneal injections of Des‐Gly10, d ‐Ala6 LHRH (LHRHa), given 3 days apart. Two injections of 100 μg kg?1 body weight of this hormone effectively induced ovulation. Within 27 days from the second injection, all fish injected with 100 μg kg?1 LHRHa had ovulated compared with 54.5% of the controls. The mean time to ovulation was reduced significantly (P<0.05) from 31.67±4.84 days in control fish and 28.83±7.31 days in sham‐treated fish to 16.36±1.61 days in fish injected with 100 μg kg?1 LHRHa. The fertilization rate in 50 and 100 μg kg?1 LHRHa‐injected fish was significantly lower than that in the control fish (P<0.05). In fish injected with 50 and 100 μg kg?1 LHRHa, significant (P<0.05) changes in testosterone (T) and 17α‐hydroxyprogestrone (OHP) levels were observed. After the second LHRHa injection, the fish injected with 100 μg kg?1 showed the highest serum levels of testosterone and OHP. These results demonstrate that the use of LHRHa can effectively reduce the mean time to ovulation and induce synchronized ovulation in Caspian brown trout.  相似文献   

4.
Wild female catfish Silurus asotus (Linnaeus, 1758) were injected with domperidone (DOM) alone, [d ‐Ala6, Pro9 Net]‐luteinizing hormone‐releasing hormone (LHRH‐A) alone once or twice, LHRH‐A plus DOM once or twice simultaneously at 6‐h intervals, LHRH‐A plus carp pituitary extract (CPE) twice simultaneously at 6‐h intervals and LHRH‐A plus human chorionic gonadotropin (HCG) twice simultaneously 6 h apart respectively. The results indicated that injection of LHRH‐A at a dosage of 0.01–0.02 μg g?1 body weight (BWt) alone induced a low but significant increase in serum gonadotropin (GtH) (P<0.05) and resulted in a very low ovulation rate, while DOM at a dosage of 5 μg g?1 BWt alone did not induce an increase in the serum GtH levels and ovulation; in contrast, LHRH‐A at a dosage of 0.01 μg g?1 BWt plus DOM at a dosage of 5 μg g?1 BWt (termed the Linpe technique) increased the serum GtH (P<0.05) significantly and induced an ovulatory rate of 100%, while LHRH‐A plus CPE or HCG resulted in an increase in the serum GtH (P<0.05) and high ovulatory rate, although the latency period was longer when fish were given LHRH‐A plus HCG or CPE.  相似文献   

5.
Kutum Rutilus frisii kutum (Kamenskii, 1901), Cyprinidae is an endemic fish of the Caspian Sea. Iranian Fisheries Organization (Shilat) produce up to 200 million fry (1–2 g body weight (b.w.)) to restock the Caspian Sea population annually. Some of these fry are produced by spawning induction in broodfish by carp pituitary extract (CPE). The objective of this study was to assay the effectiveness of the gonadotropin releasing hormone analogue (d ‐Ala6, Pro9‐Net GnRH) alone or in combination with metoclopramide (MET), a dopamine antagonist, on the percentage of ovulated females, latency period, ovulation index and fertilization success. The following hormone treatments were tested: single injection of 2 mg kg?1 b.w. of CPE as a positive control, GnRHa alone 20 and 40 μg kg?1 b.w. and combination of GnRHa and MET as follows: 5 μg+2.5 mg, 10 μg+ 5 mg and 20 μg+10 mg kg?1 b.w. Negative control group was injected with 0.7% saline. The percentage of ovulated females, ovulation index and fertilization success were 90%, 71.3±1.24%, 68.4±2.3%, respectively, in the group treated with GnRHa+MET at a dose of 20 μg+10 mg kg?1 b.w. and were significantly higher than those in the positive control (60%, 64.5±0.23%, 69.1±4.5%) (P<0.05). However, the latency period in this group was longer than that in the positive control (P<0.05). Only 20% and 40% fish ovulated in groups that received 20 or 40 μg kg?1 b.w. GnRHa. No fish ovulated in the negative control.  相似文献   

6.
A reliable breeding technique was developed for the mangrove red snapper, Lutjanus argentimaculatus (Forsskal 1775), to help sustain the aquaculture of this immensely popular species in Southeast Asia. Using standardized indices of female maturity (based on mean oocyte diameter of ≥0.40 mm), time of injection (1000–1130) and sex ratio (one female to two males), a single injection of 100 μg kg?1 luteinizing hormone‐releasing hormone analogue (LHRHa) (n=16 fish), but not 50 μg kg?1 (n=five fish), successfully induced egg (62.5% success rate) and larval (43.8%) production. Human chorionic gonadotropin (hCG) at 500 IU kg?1 (n=five fish) also failed to induce spawning, but doses of 1000 (n=22 fish) and 1500 IU kg?1 (n=15 fish) gave spawning (77.3% and 80.0% respectively) and hatching success rates (72.7% and 60.0% respectively) that were not significantly different from those of 100 μg kg?1 LHRHa. No spawning was observed in saline‐injected controls (n=seven fish). While mean spawning latency, egg diameter, egg production per spawn, percent egg viability, hatching rate, percent of normal larvae and cumulative survival of eggs to normal larvae did not differ significantly among the effective hormones and doses, 1000 IU kg?1 hCG had a higher percentage (76.5%) of total spawns with egg production per spawn in excess of one million than those of 1500 IU kg?1 hCG (50.0%) and 100 μg kg?1 LHRHa (40.0%). Mangrove red snapper spontaneously spawned from March–April to November–December with a peak of egg collection and spawning in May–June. Egg collection per spawn ranged from 0.05 to 6.35 million. Spontaneous spawning of mangrove red snapper exhibited lunar periodicity with spawns mostly occurring 3 days before or after the last quarter and new moon phases and occurred consistently between 02:00 and 04:00 hours. High fecundity and good egg quality, coupled with the ability to respond to induce spawning or natural spawning in captivity, provide a sound basis for improving the sustainability of red snapper aquaculture in Southeast Asia.  相似文献   

7.
Induced spawning in bream, Abramis brama (L), was studied using acetone-dried common carp pituitary (CP) and bream pituitary (BP) with or without the addition of human chorionic gonadotrophin (hCG). The total dose administered to fish was of 5.0 mg kg?1 BP or 4.0 mg kg?1 CP with or without 2000-2200 IU hCG kg?1 for females and 2.5 mg kg?1 BP or 2.0 mg kg?1 CP with or without 1000–1100 IU HCG kg?1 for males. In all male treated groups 100% of spermiation was observed: in females the most effective method was a triple injection with hCG and carp pituitary, resulting in 79% of females ovulated (over 68% of eyed eggs). Biological quality of eggs, expressed as a percentage of eyed eggs, was negatively correlated with time elapsing between resolving (final) injection and ovulation. Spawning success, expressed as a value of Se (spawning effectiveness coefficient), was higher in fish treated with triple injection.  相似文献   

8.
Mature black sea bass, Centropristis striata L. (200–800 g), were captured in coastal South Carolina during the spawning season and administered hormones for ovulation induction and strip spawning. During both study years, control groups of females were incorporated into the study design and administered sham injections containing physiological saline solution. In 2004, females received a single intramuscular injection of human chorionic gonadotropin (hCG) (330 IU kg−1) (n=8) or two injections of hCG at 24‐h intervals (n=8). In 2005, females received a single injection of hCG (n=10) or an analogue of luteinizing hormone releasing hormone (LHRHa) (n=10). In 2004, all fish administered a single dose of hCG ovulated at least once. Six fish ovulated on two consecutive days and one fish ovulated on 3 days consecutively. In contrast, six of eight fish receiving two doses of hCG ovulated once, five ovulated on 2 days successively and three fish ovulated 3 days in succession. Of the fish that spawned, no differences were found in any reproductive parameters. In 2005, all fish administered hCG or LHRHa ovulated at least once. Three fish administered hCG ovulated twice, four fish ovulated on three consecutive days and one fish 4 days successively. All fish administered LHRHa spawned at least twice, six fish ovulated thrice and three fish ovulated 4 days, successively. A significant difference in fertility was found between hCG (75.6±11.4%) and LHRHa (55.6±27.4%). The results of this study indicate that both hCG and LHRHa are effective for ovulation induction in prespawning black sea bass.  相似文献   

9.
Hatchery-produced white bass (Morone chrysops) and striped bass (M. saxatilis) reared to maturity in a commercial aquaculture facility, were successfully spawned using controlled-release delivery systems containing the gonadotropin-releasing hormone analog DAla6, Pro9[NEt]-GnRH (GnRHa). Two-year-old white bass females (mean weight, 0.81 kg) were implanted with different polymer-based, GnRHa delivery systems at doses ranging from 40 to 89 μg GnRHa kg−1 body weight. GnRHa treatment on 20 February 1994, when females contained oocytes up to 720 μm in diameter, induced ovulation of all fish between 35 to 82 h after treatment. The white bass eggs produced were fertilized with sperm from striped bass for the production of sunshine bass. An average of 294500 eggs kg−1 were produced, with a mean fertility of 81.2%, 24 h survival of 46.5%, and overall hatching success of 45%. Survival from hatch to 30 days post-hatch was 78% and the fry weighed between 0.07 and 0.1 g. Overripening of eggs began within 1 h from ovulation and maximum fertilization (60%) was observed when eggs were stripped 0.5 h after ovulation. Fertilization success decreased thereafter to 31% and 10% by 1 h and 3 h after ovulation, respectively. Control fish not treated with GnRHa did not show any signs of final oocyte maturation during the period of the study. GnRHa administration via controlled-release delivery systems appears to be a very effective method for inducing high fecundity ovulation of captive white bass broodstocks, and producing eggs of high fertility and hatching success.  相似文献   

10.
2007-2008年对39尾,4～5龄,雌鱼体长36～41 cm,体质量 2.5～2.9 kg,雄鱼体长 32～35 cm,体质量 1.5～1.6 kg的缺帘鱼亲鱼用 HCG、PG、LHR-A_2、DOM 4种催产药物,按5种组合(设置每千克体质量:HCG 300 IU + LHR-A_2 2.5 μg + DOM 2 mg、 HCG 3500 IU +PG 2 mg + LHR-A_2 3 μg + DOM 3 mg、PG 4 mg + LHR-A_2 6 μg + DOM 2 mg、HCG 700 IU + DOM 2 mg、LHR-A_2 5 μg + DOM 4 mg)进行催产试验,催产水温27～28 ℃,采用两针注射,效应时间 9～10h.5种组合的平均催产率分别为75.2%、75.4%、75.5%、60%、60.3%;平均受精率为76.6%;平均孵化率为68.5%;平均出苗率为72.2%;出膜时间为17～18 h;孵化水温27～28 ℃,20尾雌鱼共产卵59 560粒;共获苗种23 469尾.  相似文献   

11.
Trials on induced breeding of the native Amazonian fish tambaqui, Colossoma macropomum (Cuvier), using CPE and HCG treatments, were carried out during 1992-93 at the Fish Culture Station in Natal, Brazil. Final maturation, ovulation and spermiation of tambaqui broodstock, reared in earthen ponds, were induced by injecting heteroplastic carp pituitary gland extracts (CPE) and human chorionic gonadotrophin (HCG) separately. The female spawners received double injections and the males received a single dose. Females were tranquillized using quinaldine and their genital openings were sutured before the resolving injection was administered. Latent period between the resolving injection and ovulation varied from 6 to 11 h according to the prevailing water temperature. Milt was obtained by extrusion. Stripping and dry fertilization of the eggs produced viable larvae. Relative fecundity was estimated at 140 000 eggs kg-1. Mean fertilization and hatching rates varied from 50% to 70% and from 60% to 80%, respectively.  相似文献   

12.
The effects of dietary astaxanthin supplemented at 0, 40, 80 or 150 mg astaxanthin kg−1 on growth, survival, moult frequency, osmoregulatory capacity (OC) and selected metabolic and haematological variables in Litopenaeus vannamei acclimated to low‐salinity water (3 g L−1) were evaluated. Supplemented astaxanthin at 80 mg kg−1 improved growth, survival and moult frequency in shrimp. The lowest OC was also exhibited in shrimp fed with dietary astaxanthin at 80 mg kg−1. Shrimp haemolymph concentrations of glucose, lactate, haemocyanin and total haemocyte count were all significantly enhanced by feeding the diet supplemented with 80 mg astaxanthin kg−1 compared with shrimp fed with the other diets. On the basis of these results, dietary astaxanthin supplementation of 80 mg kg−1 is recommended for juvenile L. vannamei cultured in low‐salinity water.  相似文献   

13.
An experiment was conducted to compare the potency of different levels of luteinizing hormone-releasing hormone analogue (LHRHa) for increasing the sperm counts in sexually mature male Oreochromis niloticus (L.). One hundred males (106.49 ± 3.59g, 15.2 7 ± 0.20 cm) were randomly distributed in four treatment groups, each receiving intramuscular injections of: (i) control, 0.05 ml phosphate-buffered saline, (ii) 10 μg kg-1 LHRHa, (iii) 20 μ kg-1 LHRHa and (iv) 30 μ kg-1 LHRHa. Sperm counts were determined prior to injection (day 0) and for four consecutive days (days 1 to 4) thereafter. Results showed a significant increase in sperm counts (P < 0.01) 1 day after injection among males injected with 10 to 20 μ kg-1 LHRHa. The effect of injecting 30 μ kg-1 LHRHa is similar to that in the control group. Across all treatments, sperm counts declined with time over the 4-day sampling period.  相似文献   

14.
Pikeperch were induced to spawn 3 months prior to the natural spawning period through photothermal and hormonal stimulation. Females (five specimens in each group) were stimulated with injection of human chorionic gonadotropin (hCG) once (200 IU kg–1), twice (200 IU kg–1, second dose after 48 h–400 IU kg–1) or three times (200 IU kg–1, after 24 h–200 IU kg–1 and after another 24 h–200 IU kg–1). The control group was injected once with 0.9% NaCl. The males were stimulated with a single hormone dose of 200 IU kg–1. Eggs were obtained from all the hormonally treated fish. None of the control group females, which were only stimulated photothermally, ovulated any eggs. The time of ovulation was 66–71 h following the first injection, and the eggs viability until the eyed stage (from 71.5 to 77.5%) did not depend on the number of hormone doses (P > 0.05). The out-of-season spawning method described in this paper could be used to provide pikeperch larvae for intensive culture systems (recirculating water systems) before natural spawning season and to produce larger-sized pikeperch fingerlings for stocking.  相似文献   

15.
Induced spawning in Eurasian perch, Perca fluviatilis L., was studied using human chorionic gonadotrophs (hCG) or acetone-dried common carp pituitary with or without hCG. The dose administered to fish was 5700 IU hCG kg-1 or 4.0 mg kg-1 carp pituitary with or without 500-700 IU hCG kg-1 for females and 2850 IU hCG kg-1 or 2.0 mg kg-1 carp pituitary with or without 250-350 IU hCG kg-1 for males. There were no statistically significant differences in quantity of milt in treated and control groups, although the best result was observed when males were treated with a triple injection of hCG and carp pituitary extract. Male spermiating success, expressed as a quantity of milt, was negatively correlated with fish weight. All females treated in this experiment had oocytes at the same division, so time of ovulation was highly synchronous. Spawning success, expressed as a spawning effectivity coefficient (Sc), was highest in fish treated with the triple injection. Spawning methods described in this paper were successful, even though hormones from another order of fish were used.  相似文献   

16.
This study addresses rapid methods to identify mature channel catfish, Ictalurus punctatus, females for induced spawning with luteinizing hormone releasing hormone analog (LHRHa) and common carp pituitary extract (CPE) and the effects of stage of maturity, hormone dose, season, and cannulation before hormone injection. Hormonal intervention is the most effective method for inducing maturation and spawning in channel catfish × blue catfish, Ictalurus furcatus, hybrids. A total of 80 mature channel catfish were staged for maturity based on secondary sexual characteristics and 20–30 oocytes cannulated to ascertain their maturation stage based on the position of gonadal vesicle. Twenty females were randomly assigned to one of the four hormone regimes (priming + resolving dose): CPE 2 + 8 mg/kg (CPEC); LHRHa 20 + 40 µg/kg (LHRHaL); LHRHa 20 + 60 µg/kg (LHRHaM); and LHRHa 20 + 80 µg/kg (LHRHaH) and a fifth treatment consisted of 20 females selected based on apparent maturity as evidenced by external appearance were injected with CPE, 2 + 8 mg/kg without cannulation (CPEO). Two trials were conducted in early part of the spawning season and two trials in peak season. External methods to identify maturity correlated (r = 0.63) with that of “germinal vesicle position” method to identify the stage of maturity in females. Mean percent of females that ovulated, hatched, and fry produced per kg body weight did not differ (P > 0.05) among the five hormone treatments. The mean percent females that ovulated was higher (P < 0.05) for CPE‐induced females that were identified as “excellent” females based on external examination. The performance of cannulated females did not differ (P > 0.05) with that of non‐cannulated catfish. The mean egg quality of hormone‐induced females and percent of females ovulated in response to hormone treatment established a weak but significant linear relationship (Y = 3.85 + 0.008 × ovulation, r2 = 0.39, P < 0.05).  相似文献   

17.
Ovulation was stimulated in four groups of European catfish, Silurus glanis L., using injections of des-Gly10, [D-Ala6]-LHRH Ethylamide (20 μg kg–1) and pimozide (10 mg kg–1), Ovaprim (0.33 mL kg–1), and carp pituitary extract (4 mg kg–1, in one or two doses). A higher percentage of ovulating females (producing eggs of sufficient quality) was found after the LHRH-a and Ovaprim treatments (100% and 80%) in relation to fish treated with the pituitary extract (60% and 66.67%). The greatest weight of eggs was obtained in the case of repeated hypophysation and LHRH-a (1299.69 and 1298.57 g, respectively), and the smallest after single hypophysation (1144.08 g). After 60 h of incubation, the best quality of eggs was found in the group treated with Ovaprim (62.9% of live embryos) and the poorest in the two groups which underwent hypophysation (50.41% and 50.75%). No statistically significant effect by the ovulation stimulators on the characteristic qualitative and quantitative traits of obtained eggs was ascertained.  相似文献   

18.
To determine dietary magnesium (Mg) requirements of juvenile grass carp, Ctenopharyngodon idella, magnesium sulphate was added to the basal diet at 0, 150, 300, 600, 1200, 2400 mg Mg kg−1 diet. Each diet was fed to three replicate groups of juvenile grass carp (initial weight: 7.69 ± 0.13 g) in a closed, recirculating rearing system for 76 days. No mortality or nutritional deficiency signs were observed except the growth depression in fish fed the Mg‐deficient diet. Growth performance and activities of serum superoxide dismutase (SOD), glutathione peroxidase (GPx) and lysozyme (LSZ) were highest (P <0.05) in fish fed the diet supplemented with 600 mg Mg kg−1. The serum malondialdehyde (MDA) content was higher (P <0.05) in fish fed the diets supplemented with 0 and 150 mg Mg kg−1 than that in fish fed the diets with ≥300 mg Mg kg−1. Mg concentrations both in whole‐body and vertebrae increased with the increase in dietary Mg level up to 300 mg kg−1, whereupon the response reached a plateau. Analysis by second‐order polynomial regression of weight gain, by broken‐line regression of vertebrae Mg concentration and by linear regression of whole‐body Mg retention of fish indicated that the adequate dietary Mg concentration for juvenile grass carp was 713.5, 627.7 and 469.8 mg kg−1 diet, respectively.  相似文献   

19.
The spermiation of tench males was stimulated with Supergestran containing mammalian LHRHa lecireline at the following doses: 5, 10, 20 and 40 g kg−1 b.w.; then with carp pituitary suspension (CPS) at a dose of 2 mg kg−1 b.w. and with a control of saline physiological solution. The following days, meaning 24, 48 and 72 h after injection, sperm was collected to evaluate volume and the number of sperm per male per kg body weight (B.W.) The percentage of motile sperm and velocity of spermatozoa were measured 48 h after hormonal injection, and 72 h after hormonal injection the sperm was evaluated for fertilization and hatching ability. All 42 males in experimental groups were diploid. Live weight did not differ significantly among experimental groups. The strongest stimulation of spermiation was achieved with LHRHa in dosage of 20 and 40 g kg−1 b.w. and CPS compared to males of the control group and lower dosage of LHRHa. Analysis of variance showed no significant influence of the treatment on the velocity and percentage of motile spermatozoa. The effect of different treatment on the fertilization capacity (the number of spermatozoa per egg was equilibrated) was significant. Significantly the highest quality of sperm collected 72 h after injection expressed by percentage of fertilization and hatching (62–65% fertilization and 61–64% hatching rates, respectively) was found for LHRHa in dosage of 20 and 40 g kg−1 b.w. Significantly the lowest parameters of fertilization and hatching were found for the control group, on the 12% level.  相似文献   

20.
The results of reproduction of females from Lithuanian strain B carp after ovulation stimulation with carp pituitary homogenate (CPH; 0.3+2.7 mg kg?1; group I), Ovopel (1/5+1 pellet kg?1; group II) or [d ‐Tle6, ProNHEt9] GnRH‐a (Lecirelin) with metoclopramide (15 μg kg?1+10 mg kg?1 respectively; group III) were investigated. The lowest percentage of spawning females (71%) was recorded in the group treated with CPH. In case of Ovopel or Lecirelin induced ovulation, 86% of females spawned. No statistically significant effect of the ovulation stimulator (group) on the weight of eggs was found; however, the highest mean weight of eggs (expressed both in grams and in the percentage of female body weight) was recorded for the group treated with Ovopel (1400 g and 13%). After the treatment with CPH or Lecirelin, the weight of eggs was 1140 g (11%) and 1100 g (10%) respectively. The ovulation stimulator significantly affected the percentage of live embryos after 36 and 48 h incubation of eggs (P≤0.05; P≤0.01). After treatment with [d ‐Tle6, ProNHEt9] GnRH‐a, eggs of the best quality were obtained and after 36 and 48 h incubation the mean percentages of live embryos were significantly higher than the means calculated for the remaining two groups. No statistically significant differences were found between the percentage of living embryos after 36 and 48 h incubation of groups I and II.  相似文献   

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