1991
DOI: 10.1159/000243322
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Rapid Effects of Hypoxia on the Cerebrospinal Fluid Levels of Adenosine and Related Metabolites in Newborn and One-Month-Old Piglets

Abstract: The effect of hypoxia on the levels of adenosine, inosine and hypoxanthine in the cerebrospinal fluid (CSF) was determined by HPLC in newborn (1- to 3-day-old, n = 6) and 1-month-old (n = 5) piglets. Serial CSF samples (q 60 s) were obtained from the cisterna magna during normoxia and a 5-min hypoxia test (PaO2 = 26.5 ± 2.9 Torr). In normoxia, newborns had a lower mean (± SEM) CSF concentration of adenosine (0.72 ± 0.17 vs. 2.60 ± 0.44 μM) and a higher concentration of hypoxanthine (4.88 ± 0.41 vs. … Show more

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Cited by 17 publications
(6 citation statements)
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“…39±41 Caffeine may also block specific adenosine receptors increasing the susceptibility of the cell to hypoxia. 42 A recent literature review evaluating the association between caffeine consumption in pregnancy and IUGR emphasises that there is still a controversy as to whether caffeine is a risk factor for IUGR or not. 43 The author concluded that no study published to date is free of problems.…”
Section: Discussionmentioning
confidence: 99%
“…39±41 Caffeine may also block specific adenosine receptors increasing the susceptibility of the cell to hypoxia. 42 A recent literature review evaluating the association between caffeine consumption in pregnancy and IUGR emphasises that there is still a controversy as to whether caffeine is a risk factor for IUGR or not. 43 The author concluded that no study published to date is free of problems.…”
Section: Discussionmentioning
confidence: 99%
“…Adenosine is a purine nucleoside that has long been established as a potent vasodilator in nearly all vascular beds studied, including the brain (Winn et al 1981a). In addition, plasma and intracerebral adenosine concentrations correlate inversely with arterial oxygen content in the fetal sheep (Kjellmer et al 1989;Koos et al 1994b;Suzuki & Power, 1999), newborn piglet (Laudignon et al 1991) and adult rat (Winn et al 1981b;Van Wylen et al 1986), providing evidence that adenosine is present in vasoactive concentrations during hypoxia. There are also numerous reports on the role of adenosine in regulation of cerebral blood flow during hypoxia in both the adult rat (Morii et al 1987;Simpson & Phillis, 1991;Coney & Marshall, 1998) and newborn piglet (Laudignon et al 1990;Park et al 1995;Bari et al 1998b).…”
mentioning
confidence: 94%
“…1989; Koos et al . 1994 b ; Suzuki & Power, 1999), newborn piglet (Laudignon et al . 1991) and adult rat(Winn et al .…”
mentioning
confidence: 99%
“…Although our experiments do not support the hypothesis that the endogenous opioids mediate the regulated decrease in core temperature during acute hypoxemia in newborn and older guinea pigs, there are a number of other possibilities to consider. It is possible that other neuromodulators, such as histamine or adenosine, which are known to increase during hypoxemia (18,32,36) and which are known to influence thermoregulatory control (20,34), could mediate the regulated decrease in core temperature. Furthermore, as Tamaki and Nakayama (33) have shown that hypoxia increases the activity of warm-sensitive neurons in the preoptic area of the anterior hypothalamus, it is also possible that hypoxemia had a direct effect on these thermosensitive neurons and that this mediates the regulated decrease in core temperature.…”
Section: Discussionmentioning
confidence: 99%
“…Numerous mechanisms have been suggested for the regulated decrease in core temperature during acute hypoxemia, including a direct effect of hypoxemia on thermosensitive neurons in the preoptic area of the anterior hypothalamus (33) as well as the release of various neurotransmitters and/or neuromodulators in the central nervous system [e.g., arginine vasopressin (37), adenosine (18,34,36), histamine (20,32), and endogenous opioids (23)] that influence thermoregulation. Mayfield et al (23) have recently provided evidence that endogenous opioids participate in mediating the decrease in core temperature following acute severe hypoxemia in adult mice, produced by inhalation of 4.5% oxygen for 1.5, 2.0, and 2.5 min separated by 5 min of 21% oxygen.…”
mentioning
confidence: 99%