Evaluation of the potential for using a chinook salmon (Oncorhynchus tshawytscha) pituitary extract versus bovine growth hormone to enhance the growth of coho salmon (Oncorhynchus kisutch)

1978 ◽  
Vol 56 (6) ◽  
pp. 1226-1231 ◽  
Author(s):  
David A. Higgs ◽  
Edward M. Donaldson ◽  
Jack R. McBride ◽  
Helen M. Dye
Keyword(s):  
Growth Hormone ◽  
Body Weight ◽  
Chinook Salmon ◽  
Oncorhynchus Tshawytscha ◽  
Coho Salmon ◽  
Maximum Growth ◽  
Growth Hormones ◽  
Unit Weight ◽  
Bovine Growth Hormone ◽  
Pituitary Extract

Groups of yearling coho salmon, held at 10 °C and on a 12-h photoperiod, were injected intramuscularly once weekly with 10 or 100 μg of a chinook salmon pituitary extract (oncPE)/g body weight, 0.1–10 μg (9.2 × 10−3 IU) of bovine growth hormone (bGH)/g body weight, solvent, or no treatment for 70 days.Both oncPE and bGH treatment stimulated growth in length and weight. The potency of oncPE per unit weight was about one-ninth that of bGH. The lowest effective bGH dosage was 3.2 μg/g body weight, while 10 μg/g body weight induced the maximum growth response. Coho given 100 μg of oncPE/g body weight had the highest growth rates. Condition factors of bGH-treated fish were depressed when the dosage exceeded 1.0 μg/g body weight.It is concluded that use of bGH is more economical than the available pituitary extracts or purified piscine growth hormones for coho salmon culture. Two alternatives to the use of native growth hormones in salmon culture are discussed.

Influence of bovine growth hormone on growth rate, appetite, and food conversion of yearling coho salmon (Oncorhynchus kisutch) fed two diets of different composition

1977 ◽  
Vol 55 (1) ◽  
pp. 74-83 ◽  
Author(s):  
J. R. Markert ◽  
David A. Higgs ◽  
Helen M. Dye ◽  
D. W. MacQuarrie
Keyword(s):  
Growth Hormone ◽  
Growth Rate ◽  
Body Weight ◽  
Coho Salmon ◽  
Lower Percentage ◽  
Bovine Growth Hormone ◽  
Growth Promoter ◽  
Ration Level ◽  
Diet Formulation ◽  
Treated Fish

Paired groups of yearling coho salmon at 10 °C and on a natural photoperiod were fed twice daily either Oregon moist pellets (OMP) or a diet with poultry offal (PO) as the main protein source. The fish were fed either 0.8% body weight per day (dry weight of food (g)/wet weight of fish (g)) or to satiation. Coho in one of the groups for each diet–ration combination received, by intramuscular injection, 10 μg (0.0092 IU) of bovine growth hormone (bGH) per gram body weight one time per week for 56 days. Those in the other group were not treated.Administration of bGH significantly enhanced growth and improved food and protein conversion. Ration level altered the effect of bGH on food and protein conversion as did diet formulation at satiation. The voluntary food intake of bGH-treated fish fed OMP was higher but not significantly different from that of the controls. Diet formulation differences did not significantly affect the growth rate of either bGH-treated or untreated coho at each ration level. Irrespective of the diet–ration combination, bGH administration lead to a significant decline in condition factor.At 56 days, bGH-treated fish had a significantly lower percentage of muscle protein and a significantly higher percentage of muscle water than untreated fish. At present, the use of bGH as a growth promoter for coho salmon is not economical.

scholarly journals Consequences of Piscine orthoreovirus genotype 1 (PRV‐1) infections in Chinook salmon ( Oncorhynchus tshawytscha ), coho salmon ( O. kisutch ) and rainbow trout ( O. mykiss )

2020 ◽  
Vol 43 (7) ◽  
pp. 719-728 ◽  
Author(s):  
Maureen K. Purcell ◽  
Rachel L. Powers ◽  
Torunn Taksdal ◽  
Doug McKenney ◽  
Carla M. Conway ◽  
...  
Keyword(s):  
Rainbow Trout ◽  
Chinook Salmon ◽  
Oncorhynchus Tshawytscha ◽  
Coho Salmon ◽  
Genotype 1

Influence of Bovine Growth Hormone and L-Thyroxine on Growth, Muscle Composition, and Histological Structure of the Gonads, Thyroid, Pancreas, and Pituitary of Coho Salmon (Oncorhynchus kisutch)

1976 ◽  
Vol 33 (7) ◽  
pp. 1585-1603 ◽  
Author(s):  
David A. Higgs ◽  
Edward M. Donaldson ◽  
Helen M. Dye ◽  
J. R. McBride
Keyword(s):  
Growth Hormone ◽  
Phase I ◽  
Phase Ii ◽  
Growth Rates ◽  
Coho Salmon ◽  
Oncorhynchus Kisutch ◽  
Control Fish ◽  
Histological Structure ◽  
Bovine Growth Hormone ◽  
Poor Growth

Groups of underyearling coho salmon (Oncorhynchus kisutch) were acclimated to 10 C well water and a photoperiod of 12 h L:12 h D. Excess ration (Oregon Moist Pellet) was presented daily. Doses of bovine growth hormone (5, 10, 20, 30, or 90 μg bGH/g body wt) and L-thyroxine (0.5, 5, or 30 μg T4/g) were administered over a period of 84 days (phase I) either by injection (via dorsal musculature or peritoneal cavity) or by hormone cholesterol implants into the muscle. Administration frequency of bGH and T4 was such (range 2 times/wk-1 time/3 wk) that fish theoretically received either 10 or 30 μg bGH/g per wk or 1 or 10 μg T4/g per wk. Control fish received either alkaline saline (pH 9.5) or a cholesterol pellet. After cessation of treatment the fish were observed for an additional 84 days (phase II). During phase I, growth rates (weight) for bGH fish (2.0–2.4% per day) and for T4 fish (0.97–1.1% per day) were significantly higher than those of control fish (0.42–0.59% per day). Among bGH fish, dorsal musculature injection (2 times/wk) was significantly more effective than intraperitoneal injection (1 time/2 wk).Increases in weight above control for bGH fish at 84 days ranged from 220 to 369%. Those for T4 fish extended from 47 to 78%. In phase II, control fish growth rates were higher (0.61–0.67% per day) than those for bGH fish (0.47–0.57% per day) and T4 fish (0.32–0.44% per day). Administration of bGH and T4 (high dose) caused a progressive decline in condition factor of fish from the control range. This trend was stopped and reversed in phase II.At 84 days, generally no significant differences were detected among groups for percentages of muscle water. However, some groups had significantly higher (bGH) and others lower (T4) percentages of muscle protein relative to those of control fish. Also, significant increases (T4) and decreases (bGH) in muscle lipid percentages were found. Hormone treatment altered the histological structure of the ovary, thyroid, exocrine (T4) and endocrine (bGH) pancreas, and somatotrop cells (T4) of the pituitary. A poor growth response was noted for two groups of coho administered bGH after acclimation to sea water.

Stimulation of food intake and weight gain in mature female rats by bovine prolactin and bovine growth hormone

1993 ◽  
Vol 264 (6) ◽  
pp. E986-E992 ◽  
Author(s):  
J. C. Byatt ◽  
N. R. Staten ◽  
W. J. Salsgiver ◽  
J. G. Kostelc ◽  
R. J. Collier
Keyword(s):  
Growth Hormone ◽  
Body Weight ◽  
Weight Gain ◽  
Food Intake ◽  
Body Weight Gain ◽  
Mature Female ◽  
Female Rats ◽  
Bovine Growth Hormone ◽  
Female Rat ◽  
Moisture Percentage

Recombinant bovine prolactin (rbPRL) or bovine growth hormone (rbGH) was administered to mature female rats (10/treatment group) by daily subcutaneous injection for 10 days. Doses ranged from 7 to 5,000 micrograms/day (0.03-24 mg/kg body wt). Both rbPRL and rbGH increased body weight gain and food intake, but these parameters were increased at lower doses of rbPRL (7-63 micrograms/day) than rbGH (> 190 micrograms/day). Weight gain and food intake were maximally stimulated by 190 micrograms/day rbPRL, whereas maximal increased weight gain was obtained with the highest dose of rbGH (5,000 micrograms/day). Total carcass protein was increased by both hormones; however, protein as a percentage of body weight was unchanged. Similarly, neither rbPRL nor rbGH changed the percentage of carcass moisture. Percentage of body fat was increased by rbPRL but was decreased by rbGH. Weight of the gastrointestinal tract and kidneys was increased by both hormones, but increases were in proportion to body weight gain. These data confirm that ungulate prolactin is a hyperphagic agent in the female rat. In addition, they suggest that, while prolactin stimulates growth in mature female rats, this growth is probably not via a somatogenic mechanism.

Effects of surgically and gastrically implanted radio transmitters on swimming performance and predator avoidance of juvenile chinook salmon (Oncorhynchus tshawytscha)

1998 ◽  
Vol 55 (4) ◽  
pp. 781-787 ◽  
Author(s):  
Noah S Adams ◽  
Dennis W Rondorf ◽  
Scott D Evans ◽  
Joseph E Kelly ◽  
Russell W Perry
Keyword(s):  
Body Weight ◽  
Chinook Salmon ◽  
Oncorhynchus Tshawytscha ◽  
Swimming Performance ◽  
Smallmouth Bass ◽  
Control Fish ◽  
Entire Study ◽  
Juvenile Chinook Salmon ◽  
Surgical Implants ◽  
Juvenile Chinook

Radiotelemetry data are often used to make inferences about an entire study population; therefore, the transmitter attachment method should be the one that least affects the study animal. Juvenile chinook salmon (Oncorhynchus tshawytscha) <120 mm in fork length (FL) with either gastrically or surgically implanted transmitters had significantly lower critical swimming speeds than control fish 1 and 19-23 days after tagging. For fish >120 mm FL, fish with gastric implants swam as well as controls 1 day but not 19-23 days after tagging. In contrast, fish with surgical implants swam as well as controls 19-23 days but not 1 day after tagging. During predation trials, fish with gastric or surgical implants were eaten by smallmouth bass (Micropterus dolomieu) in significantly greater numbers than controls. We do not recommend implanting transmitters (representing 4.6-10.4% of the fish's body weight) in fish <120 mm FL. Furthermore, surgical implants (representing 2.2-5.6% of the fish's body weight) may be the preferred method for biotelemetry studies of juvenile chinook salmon >120 mm FL.

Comparison of the effect of salmon gonadotropin administered by pellet implantation or injection on sexual development of juvenile male pink salmon (Oncorhynchus gorbuscha)

1978 ◽  
Vol 56 (1) ◽  
pp. 86-89 ◽  
Author(s):  
Colin N. MacKinnon ◽  
Edward M. Donaldson
Keyword(s):  
Body Weight ◽  
Chinook Salmon ◽  
Sexual Development ◽  
Oncorhynchus Tshawytscha ◽  
Pink Salmon ◽  
Mitotic Division ◽  
Oncorhynchus Gorbuscha ◽  
Juvenile Male ◽  
Time Intervals ◽  
Pink Salmon Oncorhynchus Gorbuscha

In juvenile male pink salmon complete maturity was induced by September in the year of hatching by both pellet implantation (once per 3 weeks) and injection (thrice weekly) of 1.0μg of chinook salmon (Oncorhynchus tshawytscha) gonadotropin per gram body weight. Time of onset of mitotic division of spermatogonia and rate of spermatogenesis were accelerated in the precociously mature testes. Similar doses of salmon gonadotropin injected at longer time intervals (once per week and once per 2 weeks) resulted in slower maturation.

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