Abstract

Zymosan, an immunogenic cell wall extract of Saccharomyces cerevisiae has potential for use as an experimental pyrogen. However, the short-lived sickness responses noted with intraperitoneal and intra-articular administration of zymosan limits investigations on the long-term effectiveness of antipyretic drugs. Thus, there remains a need to establish an alternative route of zymosan administration that could induce long-lived fevers and inflammation. We injected male Sprague Dawley rats (250–300 g) subcutaneously with zymosan (30 or 300 mg/kg) or saline; n = 7–8. We measured core body temperature, cage activity, food intake and body mass for 24 h after injection. Blood and brain samples were collected at 2, 8, and 18 h after injection. Zymosan (300 mg/kg) induced fever, lethargy, and anorexia, which lasted for 24 h. Zymosan-induced sickness responses were accompanied by increased blood plasma levels of interleukin (IL)-6 and tumor necrosis factor (TNF)-α; activation of inflammatory transcription factors (nuclear factor (NF) for IL-6, signal transducer and activator of transcription (STAT)-3, and NF-κB) in the hypothalamus and circumventricular organs; and increased hypothalamic mRNA expression of TNF-α, IL-1β, and IL-6 and rate-limiting enzymes for prostaglandin synthesis. Our results confirm the suitability of subcutaneous administration of zymosan for screening antipyretic and anti-inflammatory drugs in rats.

Highlights

  • Brewer’s yeast, derived from the yeast species Saccharomyces cerevisiae, is used for inducing pyrexia in pharmacological studies screening antipyretic drugs in rats (Vogel 2002; Thangaraj 2016)

  • The magnitude and duration of the increase in body temperature was dependent on the dose of zymosan injected; between 8 and 24 h after injection, rats that received 300 mg/kg had significantly greater body temperatures compared with rats that received 30 mg/kg (p < 0.01, Bonferroni)

  • Our findings show that subcutaneous injection of 300 mg/kg of zymosan increases the concentration of circulating tumor necrosis factor (TNF)-α and IL-6 (Fig. 4) and increases hypothalamic mRNA expression of TNF-α, IL-1β, and IL-6 (Fig. 8)

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Summary

Introduction

Brewer’s yeast, derived from the yeast species Saccharomyces cerevisiae, is used for inducing pyrexia in pharmacological studies screening antipyretic drugs in rats (Vogel 2002; Thangaraj 2016). Despite the potential of Brewer’s yeast to induce fever and inflammation, two responses required for antipyretic screening, there are some ethical considerations that may limit its use as a tool for routine antipyretic screening. These ethical considerations include the use of large volumes and doses of live yeast, which are associated with the development of an abscess and prolonged body mass stunting (Todd 1986; Dangarembizi et al 2018). Because of the potential animal welfare challenges associated with using live yeast as a pyrogen for routine antipyretic screening, there is a requirement to find an alternative fungal pyrogen that can induce reasonably long fevers that allow for antipyretic testing without causing unnecessary pain and suffering to the experimental animals

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