EFFECT OF SELENIUM ON OTHER
OXIDATIVE-STRESS OR INFLAMMATORY CONDITIONS
There is a growing body of
evidence to suggest that Se can alleviate conditions associated with
high levels of oxidative stress or inflammation. These include asthma (Jahnova
et al. 2002; Shaheen et al. 1999), arthritis (Peretz et
al. 2001), muscular dystrophy (Kurihara et al. 2000), cystic
fibrosis (Kauf et al. 1994), acute pancreatitis (De las Heras
Castano et al. 2000; Vaona et al, 2005), osteoarthritis (Kurz
et al. 2002), acute septicaemia [systemic inflammatory response
syndrome] (Angstwurm et al. 1999) and kwashiorkor (Ashour et
al. 1999). In addition, Schrauzer (1998) discusses the application
of selenium therapy to viral haemorrhagic fever and lymphoedema.
The association of Se with two of these conditions: asthma and acute
septicaemia, are discussed below.
Asthma
Asthma is a condition with
genetic, allergic, environmental, infectious, emotional and nutritional
components. Its underlying pathophysiology is allergic airway
inflammation. Oxidative stress contributes to the inflammatory
component of asthma (Gazdik et al, 2004). Studies have shown an
association between both low Se intake/status and low plasma/serum GPx
activity, and increased asthma risk (Stone et al, 1989; Omland et al,
2002; Qujeq et al, 2003; Shaheen et al, 2004). Supplementation of Se in
asthmatics inhibits the activity of pro-inflammatory adhesion molecules
(Jahnova et al, 2002), substantially improves immunocompetence (Gazdik
et al, 2002a), and enables a reduction in corticosteroid use (Gazdik et
al, 2002b).
People with asthma tend to have
increased oxidative activity, lowered Se status, and decreased GPx
activity. Studies which examine Se deficiency and the preventive and
clinical effects of Se supplementation on asthma, including its
immunostimulatory effects, support the concept of Se supplementation of
asthmatics (Gazdik et al, 2004).
Acute septicaemia
Clinical studies have shown that
patients with systemic inflammatory response syndrome (SIRS) and sepsis
exhibit decreased plasma Se and glutathione peroxidase activity.
Moreover, the degree of Se deficiency correlates with the severity of
the disease and the incidence of mortality. Patients with these
conditions are under severe oxidative stress, while selenoenzymes have
important roles in alleviating this, especially where lipid peroxidation
is involved. Several studies have shown that Se supplementation
improves outcomes for SIRS/sepsis patients (Forceville et al, 2001;
Gartner et al, 2001). In a prospective randomised study, mortality was
reduced from 40% to 15%, using a daily dose of 1000
µg
sodium selenite over 28 days (Zimmermann et al, 1997), while Schrauzer
(1998) reports the finding of another German study of a reduction in
mortality from 70% to 30% in the most seriously ill septicaemia
patients, who had also developed pneumonia. This study used daily
selenite doses from 500 µg,
decreasing by day 7 to 150
µg.
Thus, although these studies are not large, the findings are promising.
Adjuvant Se therapy for these conditions, which are characterised by
such high fatality rates, may become standard practice, especially in
view of widespread resistance to standard antibiotics.
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