INVESTIGATION OF THE IMMUNOMODULATOR EFFECT OF BETA GLUCAN IN THE EXPERIMENTAL INTRAABDOMINAL BACTERIEMIA MODEL WITH STAPHYLOCOCCUS AUREUS
Öz
OBJECTIVE: The purpose of this study is to investigate the immunomodulatory effect of beta glucan in an experimental model of intraabdominal bacteremia induced by S. aureus.
MATERIAL AND METHODS: Thirty Wistar albino rats were randomly divided into four groups. Staphylococcus aureus bacteremia (SAB), treatment with cefazolin, treatment with beta glucan, treatment with both cefazolin and beta glucan groups were constituted respectively. 4 mg/kg beta glucan and 100 mg/kg cefazolin were given after 12x10 8 cfu/ml 1 cc S. aureus was given intraabdominally. After two hours, 0.5 cc blood was drawn and put into blood culture bottles. Levels of Tumor necrosis factor-alpha (TNF-α), interleukin-1 (IL-1), interleukin-6 (IL-6), and Interferon gamma (IFN-γ) were evaluated after 4th, 6th and 8th hours.
RESULTS: According to the biochemical analyses; At the end of the study it was seen that beta glucan increased the level of IFN-γ at 6th hour, but did not at 4th and 8th hours. This increase became more apparent at 6 th hour when it was given with cefazolin. However IFN-γ levels were found to be higher in the group which cefazolin was given than beta glucan was. As the level of serum TNF-α was evaluated, although there was a supression at 8th hour, it was found to be higher in the group which beta glucan was given than the SAB group. Serum IL-1 levels were higher at 4th, 6th and 8th hours in the group beta glucan was given than the SAB group. Although a decline in IL-1 level was detected in the group which cefazolin was added to beta glucan at 8th hour, this level was found to be higher than the SAB group. When the serum IL-6 level was evaluated, an increase in release of IL-6 was found in the group beta glucan was given in the first 8 hours when it was compared with SAB group. When beta glucan was given with cefazolin, it was observed that IL-6 increased to the highest level at 8th hour.
CONCLUSIONS: This experimental intra-abdominal bacteremia model, demonstrated that beta glucan did not supress the production of TNF-α and IL-1, and increased the release of IL- 6 and IFN-γ, especially in the first hours. According to these results, no significant knowledge could be obtained about the benefit of using beta glucan in the treatment of experimental model of intraabdominal bacteremia.
Anahtar Kelimeler
Proje Numarası
Kaynakça
- 1. Gudiol C, Cuervo G, Shaw E, Pujol M, Carratala J. Pharmacotherapeutic options for treating Staphylococcus aureus bacteremia. Expert Opin Pharmacother. 2017;18(18):1947-63.
- 2. Heyland DK, Hopman W, Coo H, Tranmer J. McColl MA. Long-term health-related quality of life in survivors of sepsis. Short Form 36: A valid and reliable measure of health- related quality of life. Crit Care Med. 2000;28:3599–605.
- 3. Holub M, Kluckuva Z, Beneda B. Changes in lymphocytes subpopulations and CD3/DR expression in sepsis. Clin Microbiol Infect. 2000;6:657-60.
- 4. Tsiotou AG, Sakorafas GH, Anagnostopoulos G, Bramis J. Septic shock; current pathogenetic concepts from a clinical perspective. Med Sci Monit. 2005;11:76-5.
- 5. Carrow DJ. Beta-1,3-Glucan as a primary immune activator. Townsend Letter. 1996:6;84-91.
- 6. Mohagheghur N, Dawson M, Hobbs P, et al. Glucans as immunological adjuvants. Adv Exp Med Biol. 1995;383:13-2.
- 7. Sherwood ER, Varma TK, Fram RY, Lın CY, Koutrouvelıs AP, Tolıver-Kınsky TE. Glucan phosphate potentiates endotoxininduced interferon-γ expression in immunocompetent mice, but attenuates induction of endotoxin tolerance. Clinical Science. 2001;101:541–50.
- 8. Russell JA. Management of sepsis. N Engl J Med. 2006;355:1699-713.
Ayrıntılar
Birincil Dil
İngilizce
Konular
Klinik Tıp Bilimleri
Bölüm
Araştırma Makalesi
Yazarlar
Semiha Orhan
*
0000-0003-2617-6197
Türkiye
Tuna Demirdal
0000-0002-9046-5666
Türkiye
Mustafa Kabu
0000-0003-0554-7278
Türkiye
Halit Buğra Koca
0000-0002-5353-3228
Türkiye
Neşe Demirtürk
0000-0002-6186-2494
Türkiye
Yayımlanma Tarihi
17 Ocak 2022
Gönderilme Tarihi
9 Mart 2021
Kabul Tarihi
26 Mayıs 2021
Yayımlandığı Sayı
Yıl 2022 Cilt: 23 Sayı: 1
