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. 1993;473(P):72P–123P.

Proceedings of the Physiological Society, 30 June-2 July 1993, University College London Meeting: Communications

Part II

PMCID: PMC1168845

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Selected References

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  1. AXELSSON J., HOEGBERG S. G., TIMMS A. R. THE EFFECT OF REMOVING AND READMITTING GLUCOSE ON THE ELECTRICAL AND MECHANICAL ACTIVITY AND GLUCOSE AND GLYCOGEN CONTENT OF INTESTINAL SMOOTH MUSCLE FROM THE TAENIA COLI OF THE GUINEA PIG. Acta Physiol Scand. 1965 May-Jun;64:28–42. doi: 10.1111/j.1748-1716.1965.tb04151.x. [DOI] [PubMed] [Google Scholar]
  2. Ahmad A. Abolition of postprandial alkaline tide after vagotomy and its use as a screening test in the assessment of vagotomy. Br J Surg. 1986 Nov;73(11):917–919. doi: 10.1002/bjs.1800731124. [DOI] [PubMed] [Google Scholar]
  3. Bauer A. J., Reed J. B., Sanders K. M. Slow wave heterogeneity within the circular muscle of the canine gastric antrum. J Physiol. 1985 Sep;366:221–232. doi: 10.1113/jphysiol.1985.sp015793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bers D. M., Bridge J. H. Relaxation of rabbit ventricular muscle by Na-Ca exchange and sarcoplasmic reticulum calcium pump. Ryanodine and voltage sensitivity. Circ Res. 1989 Aug;65(2):334–342. doi: 10.1161/01.res.65.2.334. [DOI] [PubMed] [Google Scholar]
  5. Bryant S. M., Ryder K. O., Hart G. Effects of neuropeptide Y on cell length and membrane currents in isolated guinea pig ventricular myocytes. Circ Res. 1991 Oct;69(4):1106–1113. doi: 10.1161/01.res.69.4.1106. [DOI] [PubMed] [Google Scholar]
  6. Cavagna G. A., Dusman B., Margaria R. Positive work done by a previously stretched muscle. J Appl Physiol. 1968 Jan;24(1):21–32. doi: 10.1152/jappl.1968.24.1.21. [DOI] [PubMed] [Google Scholar]
  7. Chesnoy-Marchais D., Fritsch J. Voltage-gated sodium and calcium currents in rat osteoblasts. J Physiol. 1988 Apr;398:291–311. doi: 10.1113/jphysiol.1988.sp017043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cooke R., Franks K., Luciani G. B., Pate E. The inhibition of rabbit skeletal muscle contraction by hydrogen ions and phosphate. J Physiol. 1988 Jan;395:77–97. doi: 10.1113/jphysiol.1988.sp016909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Davis P. D., Hill C. H., Keech E., Lawton G., Nixon J. S., Sedgwick A. D., Wadsworth J., Westmacott D., Wilkinson S. E. Potent selective inhibitors of protein kinase C. FEBS Lett. 1989 Dec 18;259(1):61–63. doi: 10.1016/0014-5793(89)81494-2. [DOI] [PubMed] [Google Scholar]
  10. Davis T. M., Burrin J. M., Bloom S. R. Growth hormone (GH) release in response to GH-releasing hormone in man is 3-fold enhanced by galanin. J Clin Endocrinol Metab. 1987 Dec;65(6):1248–1252. doi: 10.1210/jcem-65-6-1248. [DOI] [PubMed] [Google Scholar]
  11. Debnam E. S., Sharp P. A. Acute and chronic effects of pancreatic glucagon on sugar transport across the brush-border and basolateral membranes of rat jejunal enterocytes. Exp Physiol. 1993 Mar;78(2):197–207. doi: 10.1113/expphysiol.1993.sp003680. [DOI] [PubMed] [Google Scholar]
  12. Debnam E. S., Thompson C. S. The effect of fasting on the potential difference across the brush-border membrane of enterocytes in rat small intestine. J Physiol. 1984 Oct;355:449–456. doi: 10.1113/jphysiol.1984.sp015430. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Dimaline R., Sandvik A. K., Evans D., Forster E. R., Dockray G. J. Food stimulation of histidine decarboxylase messenger RNA abundance in rat gastric fundus. J Physiol. 1993 Jun;465:449–458. doi: 10.1113/jphysiol.1993.sp019686. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Edwards F. R., Hirst G. D., Silverberg G. D. Inward rectification in rat cerebral arterioles; involvement of potassium ions in autoregulation. J Physiol. 1988 Oct;404:455–466. doi: 10.1113/jphysiol.1988.sp017299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Eisenberg B. R., Salmons S. The reorganization of subcellular structure in muscle undergoing fast-to-slow type transformation. A stereological study. Cell Tissue Res. 1981;220(3):449–471. doi: 10.1007/BF00216750. [DOI] [PubMed] [Google Scholar]
  16. Fenn W. O. A quantitative comparison between the energy liberated and the work performed by the isolated sartorius muscle of the frog. J Physiol. 1923 Dec 28;58(2-3):175–203. doi: 10.1113/jphysiol.1923.sp002115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Ferenczi M. A., Goldman Y. E., Simmons R. M. The dependence of force and shortening velocity on substrate concentration in skinned muscle fibres from Rana temporaria. J Physiol. 1984 May;350:519–543. doi: 10.1113/jphysiol.1984.sp015216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Goldman Y. E., Hibberd M. G., Trentham D. R. Relaxation of rabbit psoas muscle fibres from rigor by photochemical generation of adenosine-5'-triphosphate. J Physiol. 1984 Sep;354:577–604. doi: 10.1113/jphysiol.1984.sp015394. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Gollvik L., Kellerth J. O., Ulfhake B. The effects of tenotomy and compensatory hypertrophy on the postnatal development of soleus motor units in the cat. Acta Physiol Scand. 1986 Apr;126(4):565–573. doi: 10.1111/j.1748-1716.1986.tb07856.x. [DOI] [PubMed] [Google Scholar]
  20. Greaser M. L., Moss R. L., Reiser P. J. Variations in contractile properties of rabbit single muscle fibres in relation to troponin T isoforms and myosin light chains. J Physiol. 1988 Dec;406:85–98. doi: 10.1113/jphysiol.1988.sp017370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Greene L. A., Tischler A. S. Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. Proc Natl Acad Sci U S A. 1976 Jul;73(7):2424–2428. doi: 10.1073/pnas.73.7.2424. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Gwathmey J. K., Copelas L., MacKinnon R., Schoen F. J., Feldman M. D., Grossman W., Morgan J. P. Abnormal intracellular calcium handling in myocardium from patients with end-stage heart failure. Circ Res. 1987 Jul;61(1):70–76. doi: 10.1161/01.res.61.1.70. [DOI] [PubMed] [Google Scholar]
  23. Harrington W. F. A mechanochemical mechanism for muscle contraction. Proc Natl Acad Sci U S A. 1971 Mar;68(3):685–689. doi: 10.1073/pnas.68.3.685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Harris J., Clarke R. W. An analysis of adrenergic influences on the sural-gastrocnemius reflex of the decerebrated rabbit. Exp Brain Res. 1992;92(2):310–317. doi: 10.1007/BF00227973. [DOI] [PubMed] [Google Scholar]
  25. Holder D. S. Electrical impedance tomography with cortical or scalp electrodes during global cerebral ischaemia in the anaesthetised rat. Clin Phys Physiol Meas. 1992 Feb;13(1):87–98. doi: 10.1088/0143-0815/13/1/008. [DOI] [PubMed] [Google Scholar]
  26. Hu S. L., Yamamoto Y., Kao C. Y. The Ca2+-activated K+ channel and its functional roles in smooth muscle cells of guinea pig taenia coli. J Gen Physiol. 1989 Nov;94(5):833–847. doi: 10.1085/jgp.94.5.833. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Hume J. R., Harvey R. D. Chloride conductance pathways in heart. Am J Physiol. 1991 Sep;261(3 Pt 1):C399–C412. doi: 10.1152/ajpcell.1991.261.3.C399. [DOI] [PubMed] [Google Scholar]
  28. Hwang T. C., Horie M., Nairn A. C., Gadsby D. C. Role of GTP-binding proteins in the regulation of mammalian cardiac chloride conductance. J Gen Physiol. 1992 Apr;99(4):465–489. doi: 10.1085/jgp.99.4.465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Jenkins R., McMahon S. B., Bond A. B., Hunt S. P. Expression of c-Jun as a response to dorsal root and peripheral nerve section in damaged and adjacent intact primary sensory neurons in the rat. Eur J Neurosci. 1993 Jun 1;5(6):751–759. doi: 10.1111/j.1460-9568.1993.tb00539.x. [DOI] [PubMed] [Google Scholar]
  30. Johnson C. D., Rai A. S. Urine acid output as a test of completeness of vagotomy. Br J Surg. 1990 Apr;77(4):417–420. doi: 10.1002/bjs.1800770419. [DOI] [PubMed] [Google Scholar]
  31. Józsa L., Kannus P., Thöring J., Reffy A., Järvinen M., Kvist M. The effect of tenotomy and immobilisation on intramuscular connective tissue. A morphometric and microscopic study in rat calf muscles. J Bone Joint Surg Br. 1990 Mar;72(2):293–297. doi: 10.1302/0301-620X.72B2.2312572. [DOI] [PubMed] [Google Scholar]
  32. Karavolas H. J., Hodges D. R. Neuroendocrine metabolism of progesterone and related progestins. Ciba Found Symp. 1990;153:22–55. doi: 10.1002/9780470513989.ch3. [DOI] [PubMed] [Google Scholar]
  33. Keatinge W. R., Coleshaw S. R., Cotter F., Mattock M., Murphy M., Chelliah R. Increases in platelet and red cell counts, blood viscosity, and arterial pressure during mild surface cooling: factors in mortality from coronary and cerebral thrombosis in winter. Br Med J (Clin Res Ed) 1984 Nov 24;289(6456):1405–1408. doi: 10.1136/bmj.289.6456.1405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Klein C., Cunningham D. A., Paterson D. H., Taylor A. W. Fatigue and recovery contractile properties of young and elderly men. Eur J Appl Physiol Occup Physiol. 1988;57(6):684–690. doi: 10.1007/BF01075989. [DOI] [PubMed] [Google Scholar]
  35. Kline D., Kline J. T. Repetitive calcium transients and the role of calcium in exocytosis and cell cycle activation in the mouse egg. Dev Biol. 1992 Jan;149(1):80–89. doi: 10.1016/0012-1606(92)90265-i. [DOI] [PubMed] [Google Scholar]
  36. Kozlowski R. Z., Twist V. W., Brown A. M., Powell T. Flash photolysis of intracellular caged GTP gamma S increases L-type Ca2+ currents in cardiac myocytes. Am J Physiol. 1991 Nov;261(5 Pt 2):H1665–H1670. doi: 10.1152/ajpheart.1991.261.5.H1665. [DOI] [PubMed] [Google Scholar]
  37. Lakie M., Robson L. G. Thixotropy in frog single muscle fibres. Exp Physiol. 1990 Jan;75(1):123–125. doi: 10.1113/expphysiol.1990.sp003380. [DOI] [PubMed] [Google Scholar]
  38. Lakie M., Robson L. G. Thixotropy: stiffness recovery rate in relaxed frog muscle. Q J Exp Physiol. 1988 Mar;73(2):237–239. doi: 10.1113/expphysiol.1988.sp003137. [DOI] [PubMed] [Google Scholar]
  39. Lovick T. A. Serotonergic influence from nucleus raphe obscurus on neurones in the periaqueductal grey matter in the rat. Brain Res. 1993 Mar 19;606(1):92–98. doi: 10.1016/0006-8993(93)91574-c. [DOI] [PubMed] [Google Scholar]
  40. Malhotra R. K., Wakade A. R. Vasoactive intestinal polypeptide stimulates the secretion of catecholamines from the rat adrenal gland. J Physiol. 1987 Jul;388:285–294. doi: 10.1113/jphysiol.1987.sp016615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Maroudas A., Thomas H. A simple physicochemical micromethod for determining fixed anionic groups in connective tissue. Biochim Biophys Acta. 1970 Jul 21;215(1):214–216. [PubMed] [Google Scholar]
  42. McCarron J. G., Halpern W. Potassium dilates rat cerebral arteries by two independent mechanisms. Am J Physiol. 1990 Sep;259(3 Pt 2):H902–H908. doi: 10.1152/ajpheart.1990.259.3.H902. [DOI] [PubMed] [Google Scholar]
  43. McCarron J. G., McGeown J. G., Reardon S., Ikebe M., Fay F. S., Walsh J. V., Jr Calcium-dependent enhancement of calcium current in smooth muscle by calmodulin-dependent protein kinase II. Nature. 1992 May 7;357(6373):74–77. doi: 10.1038/357074a0. [DOI] [PubMed] [Google Scholar]
  44. Morgan K. G., Muir T. C., Szurszewski J. H. The electrical basis for contraction and relaxation in canine fundal smooth muscle. J Physiol. 1981 Feb;311:475–488. doi: 10.1113/jphysiol.1981.sp013599. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Narici M. V., Bordini M., Cerretelli P. Effect of aging on human adductor pollicis muscle function. J Appl Physiol (1985) 1991 Oct;71(4):1277–1281. doi: 10.1152/jappl.1991.71.4.1277. [DOI] [PubMed] [Google Scholar]
  46. Ozil J. P. The parthenogenetic development of rabbit oocytes after repetitive pulsatile electrical stimulation. Development. 1990 May;109(1):117–127. doi: 10.1242/dev.109.1.117. [DOI] [PubMed] [Google Scholar]
  47. Parker D. F., Round J. M., Sacco P., Jones D. A. A cross-sectional survey of upper and lower limb strength in boys and girls during childhood and adolescence. Ann Hum Biol. 1990 May-Jun;17(3):199–211. doi: 10.1080/03014469000000962. [DOI] [PubMed] [Google Scholar]
  48. Paul S. M., Purdy R. H. Neuroactive steroids. FASEB J. 1992 Mar;6(6):2311–2322. [PubMed] [Google Scholar]
  49. Pelzer D., Pelzer S., McDonald T. F. Properties and regulation of calcium channels in muscle cells. Rev Physiol Biochem Pharmacol. 1990;114:107–207. doi: 10.1007/BFb0031019. [DOI] [PubMed] [Google Scholar]
  50. Robertson B. E., Corry P. R., Nye P. C., Kozlowski R. Z. Ca2+ and Mg-ATP activated potassium channels from rat pulmonary artery. Pflugers Arch. 1992 Jun;421(2-3):94–96. [PubMed] [Google Scholar]
  51. Rose R. D., Rohrlich D. Counting sectioned cells via mathematical reconstruction. J Comp Neurol. 1987 Sep 15;263(3):365–386. doi: 10.1002/cne.902630305. [DOI] [PubMed] [Google Scholar]
  52. Sanguinetti M. C., Jurkiewicz N. K. Two components of cardiac delayed rectifier K+ current. Differential sensitivity to block by class III antiarrhythmic agents. J Gen Physiol. 1990 Jul;96(1):195–215. doi: 10.1085/jgp.96.1.195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Schmitt P., Sandner G., Colpaert F. C., De Witte P. Effects of dorsal raphe stimulation on escape induced by medial hypothalamic or central gray stimulation. Behav Brain Res. 1983 Jun;8(3):289–307. doi: 10.1016/0166-4328(83)90175-4. [DOI] [PubMed] [Google Scholar]
  54. Scott O. M., Vrbová G., Hyde S. A., Dubowitz V. Responses of muscles of patients with Duchenne muscular dystrophy to chronic electrical stimulation. J Neurol Neurosurg Psychiatry. 1986 Dec;49(12):1427–1434. doi: 10.1136/jnnp.49.12.1427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Smith S. H., McCaslin M., Sreenan C., Bishop S. P. Regional myocyte size in two-kidney, one clip renal hypertension. J Mol Cell Cardiol. 1988 Nov;20(11):1035–1042. doi: 10.1016/0022-2828(88)90580-9. [DOI] [PubMed] [Google Scholar]
  56. Sweeney H. L., Kushmerick M. J., Mabuchi K., Sréter F. A., Gergely J. Myosin alkali light chain and heavy chain variations correlate with altered shortening velocity of isolated skeletal muscle fibers. J Biol Chem. 1988 Jun 25;263(18):9034–9039. [PubMed] [Google Scholar]
  57. Takano M., Noma A. Distribution of the isoprenaline-induced chloride current in rabbit heart. Pflugers Arch. 1992 Feb;420(2):223–226. doi: 10.1007/BF00374995. [DOI] [PubMed] [Google Scholar]
  58. Thompson C. S., Debnam E. S. Hyperglucagonaemia: effects on active nutrient uptake by the rat jejunum. J Endocrinol. 1986 Oct;111(1):37–42. doi: 10.1677/joe.0.1110037. [DOI] [PubMed] [Google Scholar]
  59. Thornbury K. D., Hollywood M. A., McHale N. G. Mediation by nitric oxide of neurogenic relaxation of the urinary bladder neck muscle in sheep. J Physiol. 1992;451:133–144. doi: 10.1113/jphysiol.1992.sp019157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Trautwein W., Hescheler J. Regulation of cardiac L-type calcium current by phosphorylation and G proteins. Annu Rev Physiol. 1990;52:257–274. doi: 10.1146/annurev.ph.52.030190.001353. [DOI] [PubMed] [Google Scholar]
  61. Vandervoort A. A., McComas A. J. Contractile changes in opposing muscles of the human ankle joint with aging. J Appl Physiol (1985) 1986 Jul;61(1):361–367. doi: 10.1152/jappl.1986.61.1.361. [DOI] [PubMed] [Google Scholar]
  62. Verge V. M., Xu Z., Xu X. J., Wiesenfeld-Hallin Z., Hökfelt T. Marked increase in nitric oxide synthase mRNA in rat dorsal root ganglia after peripheral axotomy: in situ hybridization and functional studies. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11617–11621. doi: 10.1073/pnas.89.23.11617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Vitullo A. D., Ozil J. P. Repetitive calcium stimuli drive meiotic resumption and pronuclear development during mouse oocyte activation. Dev Biol. 1992 May;151(1):128–136. doi: 10.1016/0012-1606(92)90220-b. [DOI] [PubMed] [Google Scholar]
  64. Wang K., Wright J. Architecture of the sarcomere matrix of skeletal muscle: immunoelectron microscopic evidence that suggests a set of parallel inextensible nebulin filaments anchored at the Z line. J Cell Biol. 1988 Dec;107(6 Pt 1):2199–2212. doi: 10.1083/jcb.107.6.2199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Westra H. G., De Haan A., van Doorn J. E., de Haan E. J. IMP production and energy metabolism during exercise in rats in relation to age. Biochem J. 1986 Nov 1;239(3):751–755. doi: 10.1042/bj2390751. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Whitaker M., Patel R. Calcium and cell cycle control. Development. 1990 Apr;108(4):525–542. doi: 10.1242/dev.108.4.525. [DOI] [PubMed] [Google Scholar]
  67. Windle R. J., Forsling M. L., Guzek J. W. Daily rhythms in the hormone content of the neurohypophysial system and release of oxytocin and vasopressin in the male rat: effect of constant light. J Endocrinol. 1992 May;133(2):283–290. doi: 10.1677/joe.0.1330283. [DOI] [PubMed] [Google Scholar]
  68. Wu S. V., Sumii K., Tari A., Mogard M., Walsh J. H. Regulation of gastric somatostatin gene expression. Metabolism. 1990 Sep;39(9 Suppl 2):125–130. doi: 10.1016/0026-0495(90)90229-6. [DOI] [PubMed] [Google Scholar]
  69. Yang H., Wong H., Walsh J. H., Taché Y. Effect of gastrin monoclonal antibody 28.2 on acid response to chemical vagal stimulation in rats. Life Sci. 1989;45(25):2413–2418. doi: 10.1016/0024-3205(89)90005-2. [DOI] [PubMed] [Google Scholar]
  70. Yasin S. A., Costa A., Besser G. M., Hucks D., Grossman A., Forsling M. L. Melatonin and its analogs inhibit the basal and stimulated release of hypothalamic vasopressin and oxytocin in vitro. Endocrinology. 1993 Mar;132(3):1329–1336. doi: 10.1210/endo.132.3.8440190. [DOI] [PubMed] [Google Scholar]
  71. de Haan A. High-energy phosphates and fatigue during repeated dynamic contractions of rat muscle. Exp Physiol. 1990 Nov;75(6):851–854. doi: 10.1113/expphysiol.1990.sp003468. [DOI] [PubMed] [Google Scholar]
  72. de Haan A., Jones D. A., Sargeant A. J. Changes in velocity of shortening, power output and relaxation rate during fatigue of rat medial gastrocnemius muscle. Pflugers Arch. 1989 Feb;413(4):422–428. doi: 10.1007/BF00584493. [DOI] [PubMed] [Google Scholar]

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