du Plessis I, Mitchell D, Laburn H P, Cartmell T
Brain Function Research Unit, School of Physiology, University of the Witwatersrand Medical School, Johannesburg, South Africa.
Can J Physiol Pharmacol. 2005 Nov;83(11):1007-14. doi: 10.1139/y05-065.
We have investigated the effects of continuous subcutaneous infusion of lipopolysaccharide (LPS), muramyldipeptide (MDP), or saline on abdominal temperature and voluntary activity in unrestrained rats. Both pyrogens were infused via osmotic pumps at a rate of approximately 2 microg.kg-1.min-1 for 7 d. LPS infusion evoked a 3-d and MDP a 1-d elevation in body temperature. Night-time activity was suppressed on days 1 and 2 during LPS infusion and on day 1 of MDP infusion. Body mass was significantly decreased on infusion day 4 in rats receiving either LPS or MDP; however, the rate of weight gain had been restored by day 8 (1 d after cessation of pyrogen infusion). We further tested the body temperature response of the same experimental animals to a single subcutaneous bolus injection (250 microg/kg) of the same pyrogen that had been infused for 7 d, 2 d after cessation of pyrogen infusion (day 9). The fever response in rats receiving a bolus injection of either LPS or MDP was significantly attenuated in rats that had previously been infused with the same pyrogen. These data suggest that tolerance developed to continuous infusion of both Gram-negative and Gram-positive pyrogens, and that mechanisms of tolerance development set in early during the 7-d infusion period of both pyrogens and persisted for at least 2 d after the cessation of pyrogen infusion. We propose that cytokine intermediates were involved or required in inducing these responses to continuous infusion of both LPS and MDP.
我们研究了持续皮下输注脂多糖(LPS)、胞壁酰二肽(MDP)或生理盐水对无束缚大鼠腹部温度和自发活动的影响。两种致热原均通过渗透泵以约2微克·千克⁻¹·分钟⁻¹的速率输注7天。输注LPS引起体温升高3天,输注MDP引起体温升高1天。在输注LPS的第1天和第2天以及输注MDP的第1天,夜间活动受到抑制。接受LPS或MDP输注的大鼠在输注第4天时体重显著下降;然而,到第8天(停止输注致热原后1天)体重增加速率已恢复。我们进一步测试了同一实验动物在停止输注致热原2天后(第9天)对皮下单次推注(250微克/千克)相同致热原的体温反应。在先前已输注相同致热原的大鼠中,接受LPS或MDP推注的大鼠的发热反应显著减弱。这些数据表明,对革兰氏阴性和革兰氏阳性致热原的持续输注均产生了耐受性,并且耐受性发展机制在两种致热原的7天输注期早期就已开始,并在停止输注致热原后至少持续2天。我们提出细胞因子中间体参与或介导了对LPS和MDP持续输注的这些反应。