Actions of β-endorphin peptides on the contractions of mouse diaphragm muscle

Peptides

Volumn 18, Issue 1, 1997, Pages 87-92

  Khan, Salim ^a   Smith, Margaret E ^a  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

Author keywords

endorphin; endorphin C terminal peptides; endorphin((1 27)); contractile responses; muscle tension; neuromuscular junction; opioids; skeletal muscle

Indexed keywords

BETA ENDORPHIN; BETA ENDORPHIN DERIVATIVE; BETA ENDORPHIN[1-27]; NALOXONE; OPIATE RECEPTOR; PEPTIDE HORMONE;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DIAPHRAGM MUSCLE; FEMALE; HORMONE ACTION; MOUSE; MUSCLE CONTRACTION; MUSCLE TONE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION;

ANIMALS; BENZYLIDENE COMPOUNDS; BETA-ENDORPHIN; DIAPHRAGM; DIPEPTIDES; ELECTRIC STIMULATION; ENKEPHALIN, D-PENICILLAMINE (2,5)-; ENKEPHALINS; FEMALE; MICE; MICE, INBRED C57BL; MUSCLE CONTRACTION; NALOXONE; NALTREXONE; NARCOTIC ANTAGONISTS; NARCOTICS; NEOSTIGMINE; OLIGOPEPTIDES; PEPTIDE FRAGMENTS;

EID: 0030891057     PISSN: 01969781     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0196-9781(96)00250-1     Document Type: Article

References (25)

1. Carr D. B., Bullen B. A., Skrinar G. S., Arnold M. A., Rosenblatt M., Beitins I. Z., Martin J. B., Mcarthur J. W. Physical conditioning facilitates the exercise-induced secretion of β -endorphin and β -lipotropin in women. N. Engl. J. 05:1981;560-563.
2. Davies D. A., Smith M. E. ACTH(4-10) increases quantal content at the mouse neuromuscular junction. Brain Res. 637:1994;328-330.
3. Evans A. A. L., Hughes S., Smith M. E. Delta opioid peptide receptors in muscles from obese-diabetic and normal mice. Peptides. 16:1995;361-364.
4. Evans C., Keith D., Morrison H., Magenzo K., Edwards R. Cloning of a delta opioid receptor by functional expression. Science. 258:1992;1952-1955.
5. Evans A. A. L., Smith M. E. Distribution of opioid receptors in muscles of lean and obese-diabetic mice. Peptides. 17:1996;629-634.
6. Gutstein H. B., Bronstein D. M., Akil H. β -Endorphin processing and cellular origins in rat spinal cord. Pain. 51:1992;241-247.
7. Haynes L. W., Smith M. E. Induction of endplate specific acetylcholinesterase by β -endorphin C-terminal dipeptide in rat and chick muscle cells. Biochem. Soc. Trans. 13:1985;174-175.
8. Haynes L. W., Smith M. E. Selective inhibition of motor endplate specific acetylcholinesterase by β -endorphin and related peptides. Neuroscience. 7:1982;1007-1013.
9. Haynes L. W., Smith M. E., Li C. H. Structural requirements and species specificity of the inhibition by β -endorphin of heavy acetylcholinesterase from vertebrate skeletal muscle. Mol Pharmacol. 26:1984;45-50.
10. Haynes L. W., Smith M. E., Smyth D. G. Evidence for the neurotrophic regulation of acetylcholinesterase in immature skeletal muscle by β -endorphin. J. Neurochem. 42:1984;1542-1551.
11. Haynes L. W., Smith M. E., Li C. H. The regulation by β -endorphin and related peptides of collagen-tailed acetylcholinesterase forms in skeletal muscles of vertebrates. Stefano G. B. Handbook of comparative aspects of opioid and related neuropeptides mechanisms. II:1986;65-79 CRC Press, Boca Raton, FL.
12. Haynes L. W., Smyth D. G., Zakarian S. Immunocytochemical localisation of lipotropin C-fragment ( β -endorphin) in the developing rat spinal cord. Brain Res. 232:1982;115-128.
13. Hughes S., Smith M. E. Upregulation of the pro-opiomelanocortin gene in motoneurones after nerve section in mice. Mol. Brain Res. 25:1994;41-49.
14. Khan S., Smith M. E. Effect of β -endorphin on the contractile responses in mouse skeletal muscle. Muscle Nerve. 18:1995;1250-1256.
15. Khan S., Smith M. E. Effect of β -endorphin(1-27) and β -endorphin(30-31) on the contractile responses of mouse diaphragm in vitro. J Physiol. 487:1995;163P.
16. Kieffer B., Befort K., Gareriaux-Ruff C., Hirth C. The δ opioid receptor: Isolation of a cDNA by expression cloning and pharmacological characterisation. Proc. Natl. Acad. Sci. USA. 89:1992;12048-12052.
17. Koelle G. B. Enhancement of acetylcholinesterase synthesis by glycylglutamine: An example of a small peptide that regulates differential transcription. Trends Pharmacol. Sci. 9:1988;318-321.
18. Lotwick H. S., Haynes L. W., Ham J. Glycyl-L-glutamine stimulates the accumulation of A12 acetylcholinesterase but not of nicotinic acetylcholine receptors in quail embryonic myotubes by a cyclic-AMP-independent mechanism. J. Neurochem. 54:1990;1122-1129.
19. 2]deltorphin II in mice: Evidence for delta receptor subtypes. J. Pharm. Exp. Ther. 258:1991;583-587.
20. Morley J. S., Hayward C. F., Carter R. J., Shuster S. MPF analogue with high stability to proteolysis. Neuropeptides. 2:1981;109-114.
21. Nicholas P., Li C. H. β -Endorphin(1-27) is a naturally occurring antagonist to etorphine-induced analgesia. Proc. Natl. Acad. Sci. USA. 82:1985;3178-3181.
22. Nyquist-Battie E. C., Hagler K. E., Millington W. R. Glycyl-L-glutamine regulates the expression of asymmetric acetylcholinesterase molecular forms in cultured cardiac postnatal myocytes. J. Mol. Cell Cardiol. 25:1993;1111-1118.
23. 1 antagonist in the mouse spinal cord. Life Sci. 52:1993;769-775.
24. 1 opioid receptors are involved in intraventricular β -endorphin-induced antinociception in the mouse. Life Sci. 52:1993;211-215.
25. Zakarian S., Smyth D. G. Distribution of active and inactive forms of endorphins in rat pituitary and brain. Proc. Natl. Acad. Sci. USA. 76:1979;5972-5976.