Letter | Published:

Demonstration of Anti-Depressant or Stimulant Properties of Imipramine in Experimental Animals

Naturevolume 191pages8485 (1961) | Download Citation

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Abstract

IMIPRAMINE (I) is a drug that is related chemically to the major tranquillizers of the phenothiazine group such as chlorpromazine (II). As distinct from chlorpromazine, however, imipramine is claimed to be of considerable value in the treatment of depression, particularly of the endogenous type1–3. Pharmacologically, imipramine has many of the properties of chlorpromazine although it is quantitatively less potent. Thus in the mouse, imipramine, like chlorpromazine, reduces motor activity, prolongs hexobarbitone sleeping time, and causes a fall in rectal temperature4,5. Both imipramine and suitable doses of chlorpromazine counteract the hypothermia, ptosis, bradycardia, and diarrhœa caused by reserpine administration in rats6, and both drugs produce sedation in the cat and dog4. In the curarized cat, both drugs block the electrocortical desynchronization caused by electrical stimulation of the mesencephalic reticular formation4, although it has been suggested7 that this action of imipramine is due to atropine-like properties rather than to chlorpromazine-like sedation. Slight qualitative differences have been observed between chlorpromazine and imipramine in their action on the electrical activity recorded from certain sub-cortical areas in the rabbit. The resemblance between the pharmacological actions of these two drugs has led to the view6 that the differences between the pharmacological effects of chlorpromazine and imipramine are, at present, only quantitative, rather than qualitative. Furthermore, unlike other drugs, such as iproniazid and nialamide, used at present in the treatment of depressive illnesses, imipramine is not an inhibitor of mono-amine oxidase9. There appeared, therefore, to be no pharmacological basis for its important clinical anti-depressant properties.

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References

  1. 1

    Kuhn, R., Schweiz. mea. Wschr., 87, 1135 (1957).

  2. 2

    Azima, H., and Vispo, R. A., Amer. J. Psychiat., 115, 245 (1958).

  3. 3

    Ball, J. R. B., and Kiloh, L. G., Brit. Med. J., ii, 1052 (1959).

  4. 4

    Sigg, E. B., Canad. Psychiat. Assoc., J., 4, S 75 (1959).

  5. 5

    Domenjoz, R., and Theobold, W., Arch. Int. Pharmacodyn., 120, 450 (1959).

  6. 6

    Costa, E., Garattini, S., and Valzelli, L., Experientia, 16, 461 (1960).

  7. 7

    Bradley, P. B., and Key, B. J., Brit. J. Pharmacol., 14, 340 (1959).

  8. 8

    Van Meter, W. G., Owens, H. F., and Himwich, H. E., Canad. Psychiat. Assoc. J., 4, S 113 (1959).

  9. 9

    Pulver, von R., Exer, B., and Herrmann, B., Arzneim.-Forsch., 10, 530 (1960).

  10. 10

    Courvoisier, S., Fournel, J., Ducrot, R., Kolsky, M., and Koetschet, P., Arch. Int. Pharmacodyn., 92, 305 (1953).

  11. 11

    Maffii, G., J. Pharm., Lond., 11, 129 (1959).

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Affiliations

  1. Research Laboratories, May and Baker, Ltd., Dagenham, Essex

    • D. R. MAXWELL
    •  & HELEN T. PALMER

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https://doi.org/10.1038/191084a0

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