Hormone secretion in transgenic rats and electrophysiological activity in their gonadotropin releasing-hormone neurons

被引:3
|
作者
Gay, Vernon L. [2 ]
Hemond, Peter J. [1 ]
Schmidt, Deena [3 ]
O'Boyle, Michael P. [1 ]
Hemond, Zoe [1 ]
Best, Janet [3 ]
O'Farrell, Laura [4 ]
Suter, Kelly J. [1 ,5 ]
机构
[1] Univ Texas San Antonio, Dept Biol, San Antonio, TX USA
[2] Univ Pittsburgh, Sch Med, Dept Cellular & Mol Physiol, Pittsburgh, PA USA
[3] Ohio State Univ, Columbus, OH 43210 USA
[4] Georgia Inst Technol, Atlanta, GA 30332 USA
[5] Univ Texas San Antonio, Inst Neurosci, San Antonio, TX USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2012年 / 303卷 / 02期
基金
美国国家科学基金会;
关键词
luteinizing hormone pulses; electrophysiology; GREEN FLUORESCENT PROTEIN; PULSE-GENERATOR ACTIVITY; LUTEINIZING-HORMONE; RHESUS-MONKEY; ELECTRICAL-ACTIVITY; CASTRATED MALE; GNRH NEURONS; FEMALE MICE; LH; ESTRADIOL;
D O I
10.1152/ajpendo.00157.2012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Gay VL, Hemond PJ, Schmidt D, O'Boyle MP, Hemond Z, Best J, O'Farrell L, Suter KJ. Hormone secretion in transgenic rats and electrophysiological activity in their gonadotropin releasing-hormone neurons. Am J Physiol Endocrinol Metab 303: E243-E252, 2012. First published May 22, 2012; doi:10.1152/ajpendo.00157.2012.-Expression of GFP in GnRH neurons has allowed for studies of individual GnRH neurons. We have demonstrated previously the preservation of physiological function in male GnRH-GFP mice. In the present study, we confirm using biocytin-filled GFP-positive neurons in the hypothalamic slice preparation that GFP-expressing somata, axons, and dendrites in hypothalamic slices from GnRH-GFP rats are GnRH1 peptide positive. Second, we used repetitive sampling to study hormone secretion from GnRH-GFP transgenic rats in the homozygous, heterozygous, and wild-type state and between transgenic and Wistar males after similar to 4 yr of backcrossing. Parameters of hormone secretion were not different between the three genetic groups or between transgenic males and Wistar controls. Finally, we performed long-term recording in as many GFP-identified GnRH neurons as possible in hypothalamic slices to determine their patterns of discharge. In some cases, we obtained GnRH neuronal recordings from individual males in which blood samples had been collected the previous day. Activity in individual GnRH neurons was expressed as total quiescence, a continuous pattern of firing of either low or relatively high frequencies or an intermittent pattern of firing. In males with both intensive blood sampling (at 6-min intervals) and recordings from their GnRH neurons, we analyzed the activity of GnRH neurons with intermittent activity above 2 Hz using cluster analysis on both data sets. The average number of pulses was 3.9 +/- 0.6/h. The average number of episodes of firing was 4.0 +/- 0.6/h. Therefore, the GnRH pulse generator may be maintained in the sagittal hypothalamic slice preparation.
引用
收藏
页码:E243 / E252
页数:10
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