Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1970 Apr;38(4):667–687. doi: 10.1111/j.1476-5381.1970.tb09876.x

Mode of action of α-methylnoradrenaline on temperature and oxygen consumption in young chickens

D J Allen, K N Garg, E Marley
PMCID: PMC1702586  PMID: 5445690

Abstract

1. Temperature, oxygen consumption, electromyographic activity, plasma non-esterified fatty acids and blood sugar were estimated in conscious unrestrained young chickens under conditions of thermoneutrality (31° C) and below thermoneutrality (16° C). In some chickens carotid arterial pressure was also recorded.

2. At thermoneutrality, α-methylnoradrenaline lowered temperature and oxygen consumption in intact or chronically vagotomized chicks. α-Methylnoradrenaline was ineffective on temperature in chicks with transection of the brain-stem posterior to the hypothalamus but anterior to the respiratory centre. Hypothermia due to α-methylnoradrenaline was associated with a significant reduction of plasma non-esterified fatty acids but blood sugar was not significantly altered. Lowering of temperature by α-methylnoradrenaline occurred despite vasoconstriction which would hinder heat loss.

3. Temperature and oxygen consumption were reduced by α-methylnoradrenaline in chronically thyroidectomized chicks to the same extent as in intact chicks but recovery did not occur unless the chicks were taken from the metabolism chamber and warmed artificially. In contrast, chronically thyroidectomized chicks given replacement thyroxine were relatively resistant to α-methylnoradrenaline.

4. Oxygen consumption of tissue slices from different parts of the chick's brain, including the diencephalon, was not altered by α-methylnoradrenaline over an extensive dose range. The effects of α-methylnoradrenaline on temperature and oxygen consumption in intact chickens were unlikely, therefore, to be due to depressed metabolism of neurones.

5. In an environment below thermoneutrality (16° C) temperature was considerably reduced and carotid arterial pressure fell 40-50 mmHg. In contrast, electromyographic activity, oxygen consumption and plasma non-esterified fatty acids were markedly raised whereas blood sugar was insignificantly elevated.

6. In experiments at 16° C, α-methylnoradrenaline markedly reduced oxygen consumption although values were still higher than those at thermoneutrality. Temperature fell further, but whereas the reductions in oxygen consumption and temperature were long-lasting, electromyographic activity (shivering) was only transiently diminished. Plasma non-esterified fatty acids were reduced after α-methylnoradrenaline but not significantly so; blood sugar was not significantly altered. The time-course for recovery of oxygen consumption following a-methylnoradrenaline paralleled recovery from its blood pressure effects but the effect on oxygen consumption was not a consequence of the blood pressure changes. The effects of a-methylnoradrenaline on temperature, oxygen consumption and electromyographic activity were similar to those of another central depressant, pentobarbitone.

Full text

PDF
667

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BLASCHKO H. Amine oxidase and amine metabolism. Pharmacol Rev. 1952 Dec;4(4):415–458. [PubMed] [Google Scholar]
  2. CARLSON L. A., LILJEDAHL S. O., VERDY M., WIRSEN C. UNRESPONSIVENESS TO THE LIPID MOBILIZING ACTION OF CATECHOLAMINES IN VIVO AND VITRO IN THE DOMESTIC FOWL. Metabolism. 1964 Mar;13:227–231. doi: 10.1016/0026-0495(64)90102-7. [DOI] [PubMed] [Google Scholar]
  3. DAWKINS M. J., HULL D. BROWN ADIPOSE TISSUE AND THE RESPONSE OF NEW-BORN RABBITS TO COLD. J Physiol. 1964 Aug;172:216–238. doi: 10.1113/jphysiol.1964.sp007414. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. DUNCOMBE W. G. THE COLORIMETRIC MICRO-DETERMINATION OF NON-ESTERIFIED FATTY ACIDS IN PLASMA. Clin Chim Acta. 1964 Feb;9:122–125. doi: 10.1016/0009-8981(64)90004-x. [DOI] [PubMed] [Google Scholar]
  5. Dewhurst W. G., Marley E. Methods for quantifying behaviour and cerebral electrical activity and the effect of drugs under controlled conditions. Br J Pharmacol Chemother. 1965 Dec;25(3):671–681. doi: 10.1111/j.1476-5381.1965.tb01792.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Duncombe W. G. The colorimetric micro-determination of long-chain fatty acids. Biochem J. 1963 Jul;88(1):7–10. doi: 10.1042/bj0880007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. FELDBERG W., MYERS R. D. CHANGES IN TEMPERATURE PRODUCED BY MICRO-INJECTIONS OF AMINES INTO THE ANTERIOR HYPOTHALAMUS OF CATS. J Physiol. 1965 Mar;177:239–245. doi: 10.1113/jphysiol.1965.sp007589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. FELDBERG W., MYERS R. D. EFFECTS ON TEMPERATURE OF AMINES INJECTED INTO THE CEREBRAL VENTRICLES. A NEW CONCEPT OF TEMPERATURE REGULATION. J Physiol. 1964 Sep;173:226–231. doi: 10.1113/jphysiol.1964.sp007454. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. HARRISON T. S. Some factors influencing thyrotropin release in the rabbit. Endocrinology. 1961 Mar;68:466–478. doi: 10.1210/endo-68-3-466. [DOI] [PubMed] [Google Scholar]
  10. HILL J. B., KESSLER G. An automated determination of glucose utilizing a glucose oxidase-peroxidase system. J Lab Clin Med. 1961 Jun;57:970–980. [PubMed] [Google Scholar]
  11. Inman O. R. Nongraded dehydration and low-pressure infiltration for rapid celloidin embedding of brain tissue. Stain Technol. 1968 Mar;43(2):69–73. doi: 10.3109/10520296809115045. [DOI] [PubMed] [Google Scholar]
  12. KEY B. J., MARLEY D. E. The effect of the sympathomimetic amines on behaviour and electrocortical activity of the chicken. Electroencephalogr Clin Neurophysiol. 1962 Feb;14:90–105. doi: 10.1016/0013-4694(62)90011-1. [DOI] [PubMed] [Google Scholar]
  13. MCILWAIN H., BUDDLE H. L. Techniques in tissue metabolism. I. A mechanical chopper. Biochem J. 1953 Feb;53(3):412–420. doi: 10.1042/bj0530412. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. MOORE R. E., UNDERWOOD M. C. THE THERMOGENIC EFFECTS OF NORADRENALINE IN NEW-BORN AND INFANT KITTENS AND OTHER SMALL MAMMALS. A POSSIBLE HORMONAL MECHANSM IN THE CONTROL OF HEAT PRODUCTION. J Physiol. 1963 Sep;168:290–317. doi: 10.1113/jphysiol.1963.sp007193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Marley E., Stephenson J. D. Effects of some catecholamines infused into the hypothalamus of young chickens. Br J Pharmacol. 1969 May;36(1):194P–195P. [PMC free article] [PubMed] [Google Scholar]
  16. Marley E., Stephenson J. D. Intracerebral micro-infusions of amines in young chickens. J Physiol. 1968 May;196(2):116P–117P. [PubMed] [Google Scholar]
  17. SCOPES J. W., TIZARD J. P. The effect of intravenous noradrenaline on the oxygen consumption of new-born mammals. J Physiol. 1963 Feb;165:305–326. doi: 10.1113/jphysiol.1963.sp007058. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Singh A., Reineke E. P., Ringer R. K. Influence of thyroid status of the chick on growth and metabolism, with observations on several parameters of thyroid function. Poult Sci. 1968 Jan;47(1):212–219. doi: 10.3382/ps.0470212. [DOI] [PubMed] [Google Scholar]
  19. TATA J. R., SHELLABARGER C. J. An explanation for the difference between the responses of mammals and birds to thyroxine and tri-iodothyronine. Biochem J. 1959 Aug;72:608–613. doi: 10.1042/bj0720608. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Wekstein D. R., Zolman J. F. Sympathetic control of homeothermy in the young chick. Am J Physiol. 1968 Apr;214(4):908–912. doi: 10.1152/ajplegacy.1968.214.4.908. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES