LIMITS OF BRAIN TOLERANCE TO DAILY INCREMENTS IN SERUM SODIUM IN CHRONICALLY HYPONATRAEMIC RATS TREATED WITH HYPERTONIC SALINE OR UREA - ADVANTAGES OF UREA

被引:48
作者
SOUPART, A
STENUIT, A
PERIER, O
DECAUX, G
机构
[1] FREE UNIV BRUSSELS,SCH MED,INST INTERDISCIPLINARY RES,B-1050 BRUSSELS,BELGIUM
[2] FREE UNIV BRUSSELS,SCH MED,DEPT NEUROANAT,B-1050 BRUSSELS,BELGIUM
关键词
ANTIDIURETIC HORMONE; CENTRAL PONTINE MYELINOLYSIS; HYPERTONIC SALINE; HYPONATREMIA; UREA;
D O I
10.1042/cs0800077
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
1. At present there is no consensus about the optimal management of hyponatraemia to prevent demyelinating brain lesions. We have evaluated in a large series of rats (n = 136) the protective role of urea for the brain in the treatment of severe chronic hyponatraemia. Urea (group I, n = 51) was compared with hypertonic saline in boluses (group II, n = 46) and with hypertonic saline in divided doses (group III, n = 39). Treatment was administered intraperitoneally over 48 h. The severity of brain lesions was assessed by histological scoring. 2. For 95% of the injured animals treated with hypertonic saline, brain lesions appeared for an absolute increment in serum Na+ concentration (DELTA-S(Na+)) of 20 mmol day-1 1(-1). Above this limit neurological injuries gradually worsened, and beyond a trasition zone (DELTA-S(NA+) greater-than-or-equal-to 20 less-than-or-equal-to 23 mmol day-1 1(-1)) 89% (group III) to 100% (group II) of the animals were injured. This limit can be reached rapidly, as attested by the comparable severity of brain lesions observed in group II (mean DELTA-S(NA+) 1 h after a bolus injection, 19 mmol/1) and in group III (mean DELTA-S(Na+) 1 h after an injection, 2 mmol/l), both groups achieving similar daily DELTA-S(Na+). 3. A correction above the threshold of 20 mmol day-1 1(-1) is as toxic during the first 24 h as during the second day of the treatment. This can be deleterious even if a mildly hyponatraemic level (greater-than-or-equal-to 120 < 129 mmol/l) is achieved after 48 h. The maximum DELTA-S(Na+) over 48 h tolerated by the brain can exceed 30 mmol/l (31-42 mmol/l), with a correction of serum Na+ concentration up to a normonatraemic level, provided that the successive daily DELTA-S(Na+) was not greater than 20 mmol/l. The severity of the pre-existing hyponatraemia does not influence the outcome of the correction phase. 4. We have confirmed the protective effect of urea against the development of brain damage when used to correct hyponatraemia. The threshold of tolerance to daily DELTA-S(Na+) after urea is identical to the limit defined for hypertonic saline, but a further rise in serum Na+ concentration (range of daily DELTA-S(Na+) > 23 less-than-or-equal-to mmol/l) leads to a significantly lower incidence (47%, P < 0.01 compared with group II and P < 0.02 compared with group III) and severity (P < 0.03 compared with group II and P < 0.005 compared with group III) of neurological complications.
引用
收藏
页码:77 / 84
页数:8
相关论文
共 40 条
[11]   TREATMENT OF THE SYNDROME OF INAPPROPRIATE SECRETION OF ANTI-DIURETIC HORMONE BY UREA [J].
DECAUX, G ;
BRIMIOULLE, S ;
GENETTE, F ;
MOCKEL, J .
AMERICAN JOURNAL OF MEDICINE, 1980, 69 (01) :99-106
[12]   UREA FOR LONG-TERM TREATMENT OF SYNDROME OF INAPPROPRIATE SECRETION OF ANTI-DIURETIC HORMONE [J].
DECAUX, G ;
GENETTE, F .
BRITISH MEDICAL JOURNAL, 1981, 283 (6299) :1081-1083
[13]   HYPONATREMIA IN THE SYNDROME OF INAPPROPRIATE SECRETION OF ANTI-DIURETIC HORMONE - RAPID CORRECTION WITH UREA, SODIUM-CHLORIDE, AND WATER RESTRICTION THERAPY [J].
DECAUX, G ;
UNGER, J ;
BRIMIOULLE, S ;
MOCKEL, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1982, 247 (04) :471-474
[14]   USE OF UREA FOR TREATMENT OF WATER-RETENTION IN HYPONATRAEMIC CIRRHOSIS WITH ASCITES RESISTANT TO DIURETICS [J].
DECAUX, G ;
MOLS, P ;
CAUCHI, P ;
DELWICHE, F .
BRITISH MEDICAL JOURNAL, 1985, 290 (6484) :1782-1783
[15]   TREATMENT OF HYPONATREMIC CIRRHOSIS WITH ASCITES RESISTANT TO DIURETICS BY UREA [J].
DECAUX, G ;
MOLS, P ;
CAUCHIE, P ;
FLAMION, B ;
DELWICHE, F .
NEPHRON, 1986, 44 (04) :337-343
[16]   UREA THERAPY FOR INAPPROPRIATE ANTI-DIURETIC HORMONE-SECRETION FROM TUBERCULOUS MENINGITIS [J].
DECAUX, G ;
UNGER, J ;
MOCKEL, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1980, 244 (06) :589-590
[17]   CEREBRAL AND PONTINE MYELINOLYSIS - 2 CASES WITH FLUID AND ELECTROLYTE IMBALANCE AND HYPOTENSION [J].
FINLAYSON, MH ;
SNIDER, S ;
OLIVA, LA ;
GAULT, MH .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1973, 18 (04) :399-409
[18]   ENCEPHALOPATHY AND MYELINOLYSIS AFTER RAPID CORRECTION OF HYPONATREMIA [J].
ILLOWSKY, BP ;
LAURENO, R .
BRAIN, 1987, 110 :855-867
[19]   UREA TRANSPORT IN CENTRAL NERVOUS SYSTEM [J].
KLEEMAN, CR ;
LEVIN, E ;
DAVSON, H .
AMERICAN JOURNAL OF PHYSIOLOGY, 1962, 203 (04) :739-&
[20]   CEREBELLAR DEGENERATION IN THE RAT FOLLOWING RAPID CORRECTION OF HYPONATREMIA [J].
KLEINSCHMIDTDEMASTERS, BK ;
NORENBERG, MD .
ANNALS OF NEUROLOGY, 1981, 10 (06) :561-565