Abstract
1. The effect of human pancreatic growth hormone releasing factor (hpGHRF) on the electrical activity of dissociated rat anterior pituitary cells in culture was studied, using both the cell-attached and whole-cell modes of the patch-clamp recording technique. 2. To avoid possible wash-out of the responses, extracellular records were made from cell-attached patches. Application of hpGHRF to the cells produced rhythmic inward currents through the patches, attributable to rhythmic hyperpolarizations of the cell membrane outside the patch. The amplitude of the current oscillations was 1-8 pA and the frequency 0.05-0.4 Hz. 3. Flooding the cells with K+ ions from a small pipette containing 50 mM or 100 mM-K+ resulted in a reversible attenuation or block of the rhythmic inward currents evoked by hpGHRF, indicating that changes in K+ conductance were involved in the responses. 4. Flooding the cells with a solution containing 10 mM-EGTA blocked these rhythmic inward currents reversibly, suggesting the involvement of Ca2+ in the responses. In addition, responses were blocked by adding Co2+ (5-10 mM) to the bathing medium. The presence of tetrodotoxin (3 microM) had no effect, ruling out the participation of voltage-gated Na+ channels. 5. With whole-cell recording, the resting potential (-41.46 +/- 7.78 mV) and input resistance (5.34 +/- 3.73 G omega) of anterior pituitary cells in culture were found to be similar to those previously reported for pituitary cells and chromaffin cells with the same recording method. 6. In whole-cell experiments, application of hpGHRF (shortly prior to intracellular penetration) evoked rhythmic outward currents, associated with conductance increases, when the cells were clamped at their resting potential. The persistence of these currents in the 'voltage-clamped' cell indicated that the rhythmicity was not related to voltage-dependent phenomena. The currents disappeared within 4 min after breaking into the cell, presumably because of 'washout' of cell constituents into the pipette. 7. The reversal potential (-60 mV) of the hpGHRF-induced currents was negative to the resting potential of the cells (-41 mV), further indicating that hpGHRF would evoke rhythmic hyperpolarizations in unclamped cells, possibly due to periodic increases in K+ conductance. 8. The possible relation of these rhythmic currents to hpGHRF-induced secretion of growth hormone is discussed.
Full text
PDF















Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Adler M., Wong B. S., Sabol S. L., Busis N., Jackson M. B., Weight F. F. Action potentials and membrane ion channels in clonal anterior pituitary cells. Proc Natl Acad Sci U S A. 1983 Apr;80(7):2086–2090. doi: 10.1073/pnas.80.7.2086. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Barinaga M., Bilezikjian L. M., Vale W. W., Rosenfeld M. G., Evans R. M. Independent effects of growth hormone releasing factor on growth hormone release and gene transcription. Nature. 1985 Mar 21;314(6008):279–281. doi: 10.1038/314279a0. [DOI] [PubMed] [Google Scholar]
- Barinaga M., Yamonoto G., Rivier C., Vale W., Evans R., Rosenfeld M. G. Transcriptional regulation of growth hormone gene expression by growth hormone-releasing factor. Nature. 1983 Nov 3;306(5938):84–85. doi: 10.1038/306084a0. [DOI] [PubMed] [Google Scholar]
- Bilezikjian L. M., Vale W. W. Stimulation of adenosine 3',5'-monophosphate production by growth hormone-releasing factor and its inhibition by somatostatin in anterior pituitary cells in vitro. Endocrinology. 1983 Nov;113(5):1726–1731. doi: 10.1210/endo-113-5-1726. [DOI] [PubMed] [Google Scholar]
- Boockfor F. R., Hoeffler J. P., Frawley L. S. Analysis by plaque assays of GH and prolactin release from individual cells in cultures of male pituitaries. Evidence for functional heterogeneity within rat mammotrope and somatotrope populations. Neuroendocrinology. 1986;42(1):64–70. doi: 10.1159/000124250. [DOI] [PubMed] [Google Scholar]
- Brazeau P., Ling N., Esch F., Böhlen P., Mougin C., Guillemin R. Somatocrinin (growth hormone releasing factor) in vitro bioactivity; Ca++ involvement, cAMP mediated action and additivity of effect with PGE2. Biochem Biophys Res Commun. 1982 Nov 30;109(2):588–594. doi: 10.1016/0006-291x(82)91762-4. [DOI] [PubMed] [Google Scholar]
- Brazeau P., Vale W., Burgus R., Ling N., Butcher M., Rivier J., Guillemin R. Hypothalamic polypeptide that inhibits the secretion of immunoreactive pituitary growth hormone. Science. 1973 Jan 5;179(4068):77–79. doi: 10.1126/science.179.4068.77. [DOI] [PubMed] [Google Scholar]
- Colquhoun D., Neher E., Reuter H., Stevens C. F. Inward current channels activated by intracellular Ca in cultured cardiac cells. Nature. 1981 Dec 24;294(5843):752–754. doi: 10.1038/294752a0. [DOI] [PubMed] [Google Scholar]
- Douglas W. W. Stimulus-secretion coupling: the concept and clues from chromaffin and other cells. Br J Pharmacol. 1968 Nov;34(3):451–474. doi: 10.1111/j.1476-5381.1968.tb08474.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Douglas W. W., Taraskevich P. S. Action potentials in gland cells of rat pituitary pars intermedia: inhibition by dopamine, an inhibitor of MSH secretion. J Physiol. 1978 Dec;285:171–184. doi: 10.1113/jphysiol.1978.sp012565. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dubinsky J. M., Oxford G. S. Dual modulation of K channels by thyrotropin-releasing hormone in clonal pituitary cells. Proc Natl Acad Sci U S A. 1985 Jun;82(12):4282–4286. doi: 10.1073/pnas.82.12.4282. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dubinsky J. M., Oxford G. S. Ionic currents in two strains of rat anterior pituitary tumor cells. J Gen Physiol. 1984 Mar;83(3):309–339. doi: 10.1085/jgp.83.3.309. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dufy B., Vincent J. D., Fleury H., Du Pasquier P., Gourdji D., Tixier-Vidal A. Membrane effects of thyrotropin-releasing hormone and estrogen shown by intracellular recording from pituitary cells. Science. 1979 May 4;204(4392):509–511. doi: 10.1126/science.107590. [DOI] [PubMed] [Google Scholar]
- Fenwick E. M., Marty A., Neher E. A patch-clamp study of bovine chromaffin cells and of their sensitivity to acetylcholine. J Physiol. 1982 Oct;331:577–597. doi: 10.1113/jphysiol.1982.sp014393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Findlay I., Petersen O. H. Acetylcholine stimulates a Ca2+-dependent C1- conductance in mouse lacrimal acinar cells. Pflugers Arch. 1985 Mar;403(3):328–330. doi: 10.1007/BF00583609. [DOI] [PubMed] [Google Scholar]
- Frawley L. S., Neill J. D. A reverse hemolytic plaque assay for microscopic visualization of growth hormone release from individual cells: evidence for somatotrope heterogeneity. Neuroendocrinology. 1984 Nov;39(5):484–487. doi: 10.1159/000124025. [DOI] [PubMed] [Google Scholar]
- Gelato M. C., Merriam G. R. Growth hormone releasing hormone. Annu Rev Physiol. 1986;48:569–591. doi: 10.1146/annurev.ph.48.030186.003033. [DOI] [PubMed] [Google Scholar]
- Gershengorn M. C. Mechanism of thyrotropin releasing hormone stimulation of pituitary hormone secretion. Annu Rev Physiol. 1986;48:515–526. doi: 10.1146/annurev.ph.48.030186.002503. [DOI] [PubMed] [Google Scholar]
- Gick G. G., Zeytin F. N., Brazeau P., Ling N. C., Esch F. S., Bancroft C. Growth hormone-releasing factor regulates growth hormone mRNA in primary cultures of rat pituitary cells. Proc Natl Acad Sci U S A. 1984 Mar;81(5):1553–1555. doi: 10.1073/pnas.81.5.1553. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gorman A. L., Thomas M. V. Changes in the intracellular concentration of free calcium ions in a pace-maker neurone, measured with the metallochromic indicator dye arsenazo III. J Physiol. 1978 Feb;275:357–376. doi: 10.1113/jphysiol.1978.sp012194. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guillemin R., Brazeau P., Böhlen P., Esch F., Ling N., Wehrenberg W. B. Growth hormone-releasing factor from a human pancreatic tumor that caused acromegaly. Science. 1982 Nov 5;218(4572):585–587. doi: 10.1126/science.6812220. [DOI] [PubMed] [Google Scholar]
- Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
- Hymer W. C., Evans W. H., Kraicer J., Mastro A., Davis J., Griswold E. Enrichment of cell types from the rat adenohypophysis by sedimentation at unit gravity. Endocrinology. 1973 Jan;92(1):275–287. doi: 10.1210/endo-92-1-275. [DOI] [PubMed] [Google Scholar]
- Igusa Y., Miyazaki S. Effects of altered extracellular and intracellular calcium concentration on hyperpolarizing responses of the hamster egg. J Physiol. 1983 Jul;340:611–632. doi: 10.1113/jphysiol.1983.sp014783. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Igusa Y., Miyazaki S. Periodic increase of cytoplasmic free calcium in fertilized hamster eggs measured with calcium-sensitive electrodes. J Physiol. 1986 Aug;377:193–205. doi: 10.1113/jphysiol.1986.sp016181. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Igusa Y., Miyazaki S., Yamashita N. Periodic hyperpolarizing responses in hamster and mouse eggs fertilized with mouse sperm. J Physiol. 1983 Jul;340:633–647. doi: 10.1113/jphysiol.1983.sp014784. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ingram C. D., Bicknell R. J., Mason W. T. Intracellular recordings from bovine anterior pituitary cells: modulation of spontaneous activity by regulators of prolactin secretion. Endocrinology. 1986 Dec;119(6):2508–2518. doi: 10.1210/endo-119-6-2508. [DOI] [PubMed] [Google Scholar]
- Kidokoro Y. Spontaneous calcium action potentials in a clonal pituitary cell line and their relationship to prolactin secretion. Nature. 1975 Dec 25;258(5537):741–742. doi: 10.1038/258741a0. [DOI] [PubMed] [Google Scholar]
- Labrie F., Gagné B., Lefèvre G. Growth hormone-releasing factor stimulates adenylate cyclase activity in the anterior pituitary gland. Life Sci. 1983 Nov 28;33(22):2229–2233. doi: 10.1016/0024-3205(83)90295-3. [DOI] [PubMed] [Google Scholar]
- Leong D. A., Lau S. K., Sinha Y. N., Kaiser D. L., Thorner M. O. Enumeration of lactotropes and somatotropes among male and female pituitary cells in culture: evidence in favor of a mammosomatotrope subpopulation in the rat. Endocrinology. 1985 Apr;116(4):1371–1378. doi: 10.1210/endo-116-4-1371. [DOI] [PubMed] [Google Scholar]
- Ling N., Esch F., Böhlen P., Brazeau P., Wehrenberg W. B., Guillemin R. Isolation, primary structure, and synthesis of human hypothalamic somatocrinin: growth hormone-releasing factor. Proc Natl Acad Sci U S A. 1984 Jul;81(14):4302–4306. doi: 10.1073/pnas.81.14.4302. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lingle C. J., Sombati S., Freeman M. E. Membrane currents in identified lactotrophs of rat anterior pituitary. J Neurosci. 1986 Oct;6(10):2995–3005. doi: 10.1523/JNEUROSCI.06-10-02995.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Login I. S., Judd A. M., MacLeod R. M. Association of 45Ca2+ mobilization with stimulation of growth hormone (GH) release by GH-releasing factor in dispersed normal male rat pituitary cells. Endocrinology. 1986 Jan;118(1):239–243. doi: 10.1210/endo-118-1-239. [DOI] [PubMed] [Google Scholar]
- Marty A. Ca-dependent K channels with large unitary conductance in chromaffin cell membranes. Nature. 1981 Jun 11;291(5815):497–500. doi: 10.1038/291497a0. [DOI] [PubMed] [Google Scholar]
- Marty A., Tan Y. P., Trautmann A. Three types of calcium-dependent channel in rat lacrimal glands. J Physiol. 1984 Dec;357:293–325. doi: 10.1113/jphysiol.1984.sp015501. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maruyama Y., Peterson O. H. Single-channel currents in isolated patches of plasma membrane from basal surface of pancreatic acini. Nature. 1982 Sep 9;299(5879):159–161. doi: 10.1038/299159a0. [DOI] [PubMed] [Google Scholar]
- Mason W. T., Waring D. W. Electrophysiological recordings from gonadotrophs. Evidence for Ca2+ channels mediated by gonadotrophin-releasing hormone. Neuroendocrinology. 1985 Sep;41(3):258–268. doi: 10.1159/000124186. [DOI] [PubMed] [Google Scholar]
- Mason W. T., Waring D. W. Patch clamp recordings of single ion channel activation by gonadotrophin-releasing hormone in ovine pituitary gonadotrophs. Neuroendocrinology. 1986;43(2):205–219. doi: 10.1159/000124529. [DOI] [PubMed] [Google Scholar]
- Neher E., Sakmann B., Steinbach J. H. The extracellular patch clamp: a method for resolving currents through individual open channels in biological membranes. Pflugers Arch. 1978 Jul 18;375(2):219–228. doi: 10.1007/BF00584247. [DOI] [PubMed] [Google Scholar]
- Owen D. G., Segal M., Barker J. L. A Ca-dependent Cl- conductance in cultured mouse spinal neurones. Nature. 1984 Oct 11;311(5986):567–570. doi: 10.1038/311567a0. [DOI] [PubMed] [Google Scholar]
- Ozawa S., Kimura N. Membrane potential changes caused by thyrotropin-releasing hormone in the clonal GH3 cell and their relationship to secretion of pituitary hormone. Proc Natl Acad Sci U S A. 1979 Nov;76(11):6017–6020. doi: 10.1073/pnas.76.11.6017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ozawa S., Sand O. Electric activity of rat anterior pituitary cells in vitro. Acta Physiol Scand. 1978 Mar;102(3):330–341. doi: 10.1111/j.1748-1716.1978.tb06080.x. [DOI] [PubMed] [Google Scholar]
- Petersen O. H., Maruyama Y. Calcium-activated potassium channels and their role in secretion. Nature. 1984 Feb 23;307(5953):693–696. doi: 10.1038/307693a0. [DOI] [PubMed] [Google Scholar]
- Poulsen J. H., Williams J. A. Spontaneous repetitive hyperpolarisations from cells in the rat adenohypophysis. Nature. 1976 Sep 9;263(5573):156–158. doi: 10.1038/263156a0. [DOI] [PubMed] [Google Scholar]
- Rivier J., Spiess J., Thorner M., Vale W. Characterization of a growth hormone-releasing factor from a human pancreatic islet tumour. Nature. 1982 Nov 18;300(5889):276–278. doi: 10.1038/300276a0. [DOI] [PubMed] [Google Scholar]
- Schettini G., Cronin M. J., Hewlett E. L., Thorner M. O., MacLeod R. M. Human pancreatic tumor growth hormone-releasing factor stimulates anterior pituitary adenylate cyclase activity, adenosine 3',5'-monophosphate accumulation, and growth hormone release in a calmodulin-dependent manner. Endocrinology. 1984 Oct;115(4):1308–1314. doi: 10.1210/endo-115-4-1308. [DOI] [PubMed] [Google Scholar]
- Surprenant A. Correlation between electrical activity and ACTH/beta-endorphin secretion in mouse pituitary tumor cells. J Cell Biol. 1982 Nov;95(2 Pt 1):559–566. doi: 10.1083/jcb.95.2.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Taraskevich P. S., Douglas W. W. Action potentials occur in cells of the normal anterior pituitary gland and are stimulated by the hypophysiotropic peptide thyrotropin-releasing hormone. Proc Natl Acad Sci U S A. 1977 Sep;74(9):4064–4067. doi: 10.1073/pnas.74.9.4064. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vale W., Rivier C., Brown M. Regulatory peptides of the hypothalamus. Annu Rev Physiol. 1977;39:473–527. doi: 10.1146/annurev.ph.39.030177.002353. [DOI] [PubMed] [Google Scholar]
- Wong B. S., Lecar H., Adler M. Single calcium-dependent potassium channels in clonal anterior pituitary cells. Biophys J. 1982 Sep;39(3):313–317. doi: 10.1016/S0006-3495(82)84522-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Woods N. M., Cuthbertson K. S., Cobbold P. H. Repetitive transient rises in cytoplasmic free calcium in hormone-stimulated hepatocytes. Nature. 1986 Feb 13;319(6054):600–602. doi: 10.1038/319600a0. [DOI] [PubMed] [Google Scholar]
- Yellen G. Single Ca2+-activated nonselective cation channels in neuroblastoma. Nature. 1982 Mar 25;296(5855):357–359. doi: 10.1038/296357a0. [DOI] [PubMed] [Google Scholar]
