N-METHYL-D,L-ASPARTATE MODULATION OF PITUITARY-HORMONE SECRETION IN THE PIG - ROLE OF OPIOID-PEPTIDES

被引:15
作者
CHANG, WJ
BARB, CR
KRAELING, RR
RAMPACEK, GB
ASANOVICH, KM
机构
[1] USDA ARS,RICHARD B RUSSELL AGR RES CTR,ANIM PHYSIOL UNIT,POB 5677,ATHENS,GA 30613
[2] UNIV GEORGIA,DEPT ANIM & DAIRY SCI,ATHENS,GA 30602
关键词
D O I
10.1016/0739-7240(93)90034-9
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Sixteen ovariectomized (OVX) mature gilts, averaging 139.6 +/- 3.1 kg body weight (BW) were assigned randomly to receive either progesterone (P, 0.85 mg/kg BW, n=8) or com oil vehicle (OIL, n=8) injections im twice daily for 10 d. On the day of experiment, all gilts received either the EAA agonist, N-methyl-d,l-aspartate (NMA; 10 mg/kg BW, iv) alone or NMA plus the EOP antagonist, naloxone (NAL, 1 mg/kg BW, iv), resulting in the following groups of 4 gilts each: OIL-NMA, OIL-NMA-NAL, P-NMA and P-NMA-NAL. Blood samples were collected via jugular cannula every 15 min for 6 hr. All pigs received NMA 5 min following pretreatment with either 0.9% saline or NAL 2 hr after blood collection began and a GnRH challenge 3 hr after NMA. Administration of NMA suppressed (P<0.03) LH secretion in OIL-NMA gilts and treatment with NAL failed to reverse the suppressive effect of NMA on LH secretion in OIL-NMA-NAL gilts. Similar to OIL-NMA gilts, NMA decreased (P<0.03) mean serum LH concentrations in P-NMA gilts. However, in P-NMA-NAL gilts, serum LH concentrations were not changed following treatment. All gilts responded to GnRH with increased (P<0.01) LH secretion. Additionally, administration of NMA increased (P<0.01) growth hormone (GH) and prolactin (PRL) secretion in both OIL-NMA and P-NMA gilts, but this increase in GH and PRL secretion was attenuated (P<0.01) by pretreatment with NAL in OIL-NMA-NAL and P-NMA-NAL gilts. Serum cortisol concentrations increased (P<0.01) in all gilts and the magnitude of the cortisol response was not different among groups. In summary, results of the present study confirmed previous findings that NMA suppresses LH secretion in both oil- and P-treated OVX gilts, but we failed to provide definitive evidence that EOP are involved in the NMA-induced suppression of LH secretion. However, NMA may, in part, activate the EOP system which in turn increased GH and PRL secretion in the gilt.
引用
收藏
页码:305 / 313
页数:9
相关论文
共 32 条
[1]  
[Anonymous], 1982, SAS USERS GUIDE
[2]   DL-2-AMINO-5-PHOSPHONOPENTANOIC ACID, A SPECIFIC N-METHYL-D-ASPARTIC ACID RECEPTOR ANTAGONIST, SUPPRESSES PULSATILE LH-RELEASE IN THE RAT [J].
ARSLAN, M ;
POHL, CR ;
PLANT, TM .
NEUROENDOCRINOLOGY, 1988, 47 (05) :465-468
[3]   POSSIBLE MODULATION OF N-METHYL-D,L-ASPARTIC ACID-INDUCED PROLACTIN-RELEASE BY TESTICULAR-STEROIDS IN THE ADULT MALE RHESUS-MONKEY [J].
ARSLAN, M ;
RIZVI, SSR ;
JAHAN, S ;
ZAIDI, P ;
SHAHAB, M .
LIFE SCIENCES, 1991, 49 (15) :1073-1077
[4]  
Bach F. W., 1992, Society for Neuroscience Abstracts, V18, P500
[5]   N-METHYL-D,L-ASPARTATE STIMULATES GROWTH-HORMONE AND PROLACTIN BUT INHIBITS LUTEINIZING-HORMONE SECRETION IN THE PIG [J].
BARB, CR ;
DEROCHERS, GM ;
JOHNSON, B ;
UTLEY, RV ;
CHANG, WJ ;
RAMPACEK, GB ;
KRAELING, RR .
DOMESTIC ANIMAL ENDOCRINOLOGY, 1992, 9 (03) :225-232
[6]   OPIOID MODULATION OF GONADOTROPIN AND PROLACTIN SECRETION IN DOMESTIC FARM-ANIMALS [J].
BARB, CR ;
KRAELING, RR ;
RAMPACEK, GB .
DOMESTIC ANIMAL ENDOCRINOLOGY, 1991, 8 (01) :15-27
[7]  
BARB CR, 1982, J REPROD FERTIL, V64, P85, DOI 10.1530/jrf.0.0640085
[8]   ENDOCRINE CHANGES IN SOWS EXPOSED TO ELEVATED AMBIENT-TEMPERATURE DURING LACTATION [J].
BARB, CR ;
ESTIENNE, MJ ;
KRAELING, RR ;
MARPLE, DN ;
RAMPACEK, GB ;
RAHE, CH ;
SARTIN, JL .
DOMESTIC ANIMAL ENDOCRINOLOGY, 1991, 8 (01) :117-127
[9]   OPIOID MODULATION OF FSH, GROWTH-HORMONE AND PROLACTIN SECRETION IN THE PREPUBERAL GILT [J].
BARB, CR ;
KRAELING, RR ;
RAMPACEK, GB .
JOURNAL OF ENDOCRINOLOGY, 1992, 133 (01) :13-19
[10]   INFLUENCE OF STAGE OF THE ESTROUS-CYCLE ON ENDOGENOUS OPIOID MODULATION OF LUTEINIZING-HORMONE, PROLACTIN, AND CORTISOL SECRETION IN THE GILT [J].
BARB, CR ;
KRAELING, RR ;
RAMPACEK, GB ;
WHISNANT, CS .
BIOLOGY OF REPRODUCTION, 1986, 35 (05) :1162-1167