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Blood Bromine in the Psychoses

Published online by Cambridge University Press:  19 February 2018

T. J. Hennelly
Affiliation:
Cardiff City Mental Hospital
E. D. Yates
Affiliation:
Biochemical Laboratory, Cardiff City Mental Hospital

Extract

Early investigators differed widely in their estimations of the bromine content of normal blood (1, 2), and it was not until the development of a refined technique by Bernhardt and Ucko (3) that it was generally recognized that blood bromine varied around 1 mgrm. %. These authors gave a range of 1.0 to 1.6 mgrm. %. Their studies, however, were not extensive. During 1931–3 Zondek and Bier (4, 5, 6) published the results of a series of investigations into the bromine content of the blood of normal and psychotic patients. From a study of 150 mentally normal patients they considered that blood bromine usually varied between 0.8 and 1.0 mgrm. %, a range later extended to 0.731.10 mgrm. % as a result of further study. In a large number of psychotics examined by them, values lying within these limits were found with the notable exception that 85%-90% of 60 cases of endogenous manic-depressive psychoses gave figures 40% to 60% below their normal levels (Zondek, 1933) (6). These low figures appeared only to be associated with this psychosis, although of the 16 cases of schizophrenia examined by them, 5 gave figures lower than the normal. They stated that in these 5 cases the mental picture was characterized by more or less marked depression, and they considered the possibility of their ultimately turning out to be manic-depressive in character. In a later paper, three examples are cited of low blood bromine associated with organic brain disease, and thought to be due to interference with a bromine-regulating centre in the brain. The low values found in manic-depressive psychoses were shown to be independent of the phase, and it was stated that values in general were not subject to seasonal variations, to menstrual fluctuations, or to alterations due to variable salt intake.

Type
Part I.—Original Articles
Copyright
Copyright © Royal College of Psychiatrists, 1935 

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References

1 Justus, , Virchow's Arch., 1907, cxc, p. 594.Google Scholar
2 Damiens, , Compt. Rend. Acad., 1920, clxx, p. 930.Google Scholar
3 Bernhardt, and Ucko, , Biochem. Zeitschr., 1926, clxx, p. 459.Google Scholar
4 Zondek, and Bier, , Klin. Woch., 1932, xi, p. 633.CrossRefGoogle Scholar
5 Idem , ibid., 1933, xii, p. 55.Google Scholar
6 Zondek, , ibid., 1933, xii, p. 1411.Google Scholar
7 Uhlman, , ibid., 1932, xi, p. 1310.Google Scholar
8 Ewer, , Zeitschr. klin. Med., 1932, cxxii, p. 244.Google Scholar
9 Schneider, , Chirurg., 1931, iii, No. 13.Google Scholar
10 Klimke, and Holthaus, , Deutsch, med. Wochenschr., 1932, xl, p. 1558.Google Scholar
11 Sacristan, and Peraita, , Arch, de Neurobiol., Jan.–Feb., 1933, xiii.Google Scholar
12 Idem , Klin. Wochenschr., 1933, xii, p. 469.Google Scholar
13 Kuranami, , Journ. Biochem?(Japan), 1932, xv, p. 205.Google Scholar
14 Pincussen, and Roman, , Biochem. Zeitschr., 1929, ccvii, p. 416.Google Scholar
15 Fleischhacker, and Scheiderer, , Monats. Psych. Neur., 1933, 1xxxiv, p. 348.Google Scholar
16 Hahn, , Klin. Wochenschr., 1933, xii, p. 390.Google Scholar
17 Holtz, and Roggenbau, , ibid., 1933, xii, p. 1410.Google Scholar
18 Urechia, and Retezeaunu, , C. R. Soc. Biol., 1933, cxii, p. 411.Google Scholar
19 Idem , ibid., 1934, cxv, p. 312.Google Scholar
20 Guillaumin, and Merejkowsky, , ibid., 1933, xciii, p. 1428.Google Scholar
21 Guillaumin, , Progrès Méd., 1933, xlviii, p. 1.Google Scholar
22 Yates, , Biochem. Journ., 1933, xxvii, p. 1763.Google Scholar
23 Bobtelski, and Rososkaja-Roseinskaja, Zeitschr. anorg. Chem., 1931, cxcix, p. 283.Google Scholar
24 Francis, and Harvey, , Biochem. Journ., 1933, xxvii, p. 1545.Google Scholar
25 Baur, and Oppenheimer, , Arch. Exper. Path. Pharm., 1922, xciv, p. 1.Google Scholar
26 M⊘ller, , ibid., 1932, clxv, p. 244.Google Scholar
27 Damiens, and Blaignan, , Compt. Rend., 1932, cxciv, p. 2077.Google Scholar
28 Harkins, Hastings and Liu, , Journ. Biol. Chem., 1931–2, xciv, p. 681.Google Scholar
29 Kuranami, , Journ. Biochem. (Japan), 1933, xviii, p. 417.CrossRefGoogle Scholar
30 Quastel, and Yates, , Biochem. Journ., 1934, xxviii, p. 1530.Google Scholar
31 Robertson, , Lancet, 1927, p. 322.Google Scholar
32 Close, , Biochem. Journ., 1933, xxvii, p. 967.Google Scholar
33 Parfitt, , Brit. Med. Journ., 1933 (1), p. 1102.Google Scholar
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