scholarly journals Dose-Response of Sodium Bicarbonate Ingestion Highlights Individuality in Time Course of Blood Analyte Responses

Author(s):  
Rebecca Louise Jones ◽  
Trent Stellingwerff ◽  
Guilherme Giannini Artioli ◽  
Bryan Saunders ◽  
Simon Cooper ◽  
...  

To defend against hydrogen cation accumulation and muscle fatigue during exercise, sodium bicarbonate (NaHCO3) ingestion is commonplace. The individualized dose-response relationship between NaHCO3 ingestion and blood biochemistry is unclear. The present study investigated the bicarbonate, pH, base excess and sodium responses to NaHCO3 ingestion. Sixteen healthy males (23 ± 2 years; 78.6 ± 15.1 kg) attended three randomized order-balanced, nonblinded sessions, ingesting a single dose of either 0.1, 0.2 or 0.3 g·kg-1BM of NaHCO3 (Intralabs, UK). Fingertip capillary blood was obtained at baseline and every 10 min for 1 hr, then every 15 min for a further 2 hr. There was a significant main effect of both time and condition for all assessed blood analytes (p ≤ .001). Blood analyte responses were significantly lower following 0.1 g·kg-1BM compared with 0.2 g·kg-1BM; bicarbonate concentrations and base excess were highest following ingestion of 0.3 g·kg-1BM (p ≤ .01). Bicarbonate concentrations and pH significantly increased from baseline following all doses; the higher the dose the greater the increase. Large interindividual variability was shown in the magnitude of the increase in bicarbonate concentrations following each dose (+2.0–5; +5.1–8.1; and +6.0–12.3 mmol·L-1 for 0.1, 0.2 and 0.3 g·kg-1BM) and in the range of time to peak concentrations (30–150; 40–165; and 75–180 min for 0.1, 0.2 and 0.3 g·kg-1BM). The variability in bicarbonate responses was not affected by normalization to body mass. These results challenge current practices relating to NaHCO3 supplementation and clearly show the need for athletes to individualize their ingestion protocol and trial varying dosages before competition.

Anaesthesia ◽  
1991 ◽  
Vol 46 (11) ◽  
pp. 907-911 ◽  
Author(s):  
L. M. LAMBALK ◽  
A. P. M. WIT ◽  
J. M. K. H. WIERDA ◽  
P. J. HENNIS ◽  
S. AGOSTON

2021 ◽  
Vol 26 ◽  
pp. 100927
Author(s):  
Dorcas Ibukun Akinloye ◽  
Regina Ngozi Ugbaja ◽  
Oluwatosin Adebisi Dosumu ◽  
Samson Adisa Rahman ◽  
Emmanuel Ifeanyichukwu Ugwor ◽  
...  

1970 ◽  
Vol 48 (2) ◽  
pp. 157-165 ◽  
Author(s):  
J. KYNČL ◽  
J. RUDINGER

SUMMARY The rate of excretion of antidiuretic activity in the urine of anaesthetized, water-loaded cats and of rats with familial diabetes insipidus after injection of single doses of lysine vasopressin (LVP) and of the long-acting analogue Nα-glycyl-glycyl-glycyl-[8-lysine]-vasopressin (triglycylvasopressin) has been studied by assays in water-loaded rats. The excreted antidiuretic material in all experiments resembled LVP and differed from triglycylvasopressin in the time course of the recorded response, the slope of the log dose—response relationship, and the index of persistence. The total antidiuretic activity excreted was a fraction of that of the injected LVP but equalled or exceeded the assayable activity of the dose of triglycylvasopressin injected. It is concluded that the excreted antidiuretic activity is due to LVP and that the excreted hormone originates from the triglycylvasopressin by enzymic activation in vivo.


1962 ◽  
Vol 41 (2) ◽  
pp. 268-273 ◽  
Author(s):  
Ralph I. Dorfman

ABSTRACT The stimulating action of testosterone on the chick's comb can be inhibited by the subcutaneous injection of 0.1 mg of norethisterone or Ro 2-7239 (2-acetyl-7-oxo-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydrophenanthrene), 0.5 mg of cortisol or progesterone, and by 4.5 mg of Mer-25 (1-(p-2-diethylaminoethoxyphenyl)-1-phenyl-2-p-methoxyphenyl ethanol). No dose response relationship could be established. Norethisterone was the most active anti-androgen by this test.


Sign in / Sign up

Export Citation Format

Share Document