Plasma gonadotropin, 17β-estradiol, and 17α,20β-dihydroxy-4-pregnen-3-one levels during luteinizing hormone-releasing hormone analogue and gonadotropin induced ovulation in coho salmon (Oncorhynchus kisutch)

1985 ◽  
Vol 63 (4) ◽  
pp. 824-833 ◽  
Author(s):  
Glen Van Der Kraak ◽  
Helen M. Dye ◽  
Edward M. Donaldson ◽  
George A. Hunter

Intraperitoneal injections of des Gly10-(D-Ala6) luteinizing hormone-releasing hormone ethylamide (LH-RHA DAla6) alone and in combination with partially purified chinook salmon gonadotropin (SG-G100) were shown to be highly effective means of inducing ovulation in coho salmon. Two injections of LH-RHA DAla6 72 h apart or LH-RHA DAla6 injected with or 72 h following an injection of SG-G100 induced ovulation in 6–10 days. The induction of ovulation was associated with the duration rather than the initial magnitude of the increase in plasma gonadotropin levels. Plasma 17β-estradiol levels decreased whereas plasma 17α,20β-dihydroxy-4-pregnen-3-one (17α20βP) levels increased in response to elevated plasma gonadotropin levels. The time of ovulation was related to the magnitude and rate of change in plasma 17β-estradiol and 17α20βP levels. Ovulation occurred following a reduction of plasma 17β-estradiol levels to less than 2 ng/mL and this decline preceded or was concomitant with an increase in plasma 17αt20βP levels to 450–500 ng/mL. 17α20βP levels in fish which underwent oocyte maturation but not ovulation were lower (100 ng/mL), suggesting that high levels of 17α20βP may have a direct role in ovulation. Changes in 17β-estradiol production appear to determine the time of ovulation by influencing the magnitude and rate of increase of plasma 17α20βP levels.

1976 ◽  
Vol 54 (3) ◽  
pp. 405-408 ◽  
Author(s):  
M. A. Hirsch ◽  
M. L. Givner

An in vivo method for the determination of biological potency of luteinizing hormone -releasing hormone (LH–RH) antiserum is described. The procedure involves antiserum blockade of LH–RH induced ovulation in immature rats primed with pregnant mare's serum. A modified method for the induction of LH–RH antibodies in rabbits is also detailed.


1982 ◽  
Vol 39 (4) ◽  
pp. 627-632 ◽  
Author(s):  
Stacia A. Sower ◽  
Carl B. Schreck ◽  
Edward M. Donaldson

Coho salmon (Oncorhynchus kisutch) mature and spawn naturally in fresh water. We investigated the feasibility of accelerating maturation and/or ovulation of coho salmon retained in seawater during the spawning season, and compared accelerated ovulation of coho salmon in seawater and in fresh water. Effective inducers of ovulation in salmon held in fresh water were partly purified or purified salmon gonadotropin followed 3 d later by luteinizing hormone releasing hormone analogue (LH-RHa); one injection of salmon pituitary extract (SPE); chum salmon pituitary (PIT) followed at 3 d by PIT; and one injection of 17α-hydroxy-20β-dihydroprogesterone. One injection of chinook SPE; coho SPE followed at 3 d by coho SPE; or partly purified or purified salmon gonadotropin followed at 3 d by LH-RHa were effective but to a much lesser extent in those salmon held in seawater. PIT followed at 3 d by PIT, or one injection of 17α-hydroxy-20β-dihydroprogesterane were ineffective in acceleration of maturation/ovulation of coho salmon retained in seawater. Cortisone or 20β-hydroxyprogesterone, which were only tested in salmon in seawater, also failed to elicit early ovulation compared with controls. We conclude that ovarian responses to the treatments of fish retained in seawater are reduced by osmoregulatory difficulties or high adult mortalities. Thus acceleration of ovulation of coho salmon held in seawater is not feasible at this time and requires further research.Key words: coho salmon, spawning, ovulation, induced breeding, gonadotropin, luteinizing hormone releasing hormone analogue


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