Madahi Palma-Gómez, Ivan Osnaya, Adriana Balderas, Diana Ortega, Carolina Escobar
a Facultad de Medicina , Universidad Nacional Autónoma de México, UNAM , Mexico City , México.
Chronobiol Int. 2018 Aug;35(8):1153-1167. doi: 10.1080/07420528.2018.1465070. Epub 2018 Apr 24.
Exposure to light at night is a disruptive condition for the adult circadian system, leading to arrhythmicity in nocturnal rodents. Circadian disruption is a risk factor for developing physiological and behavioral alterations, including weight gain and metabolic disease. During early stages of development, the circadian system undergoes a critical period of adjustment, and it is especially vulnerable to altered lighting conditions that may program its function, leading to long-term effects. We hypothesized that during lactation a disrupted light-dark cycle due to light at night may disrupt the circadian system and in the long term induce metabolic disorders. Here we explored in pups, short- and long-term effects of constant light (LL) during lactation. In the short term, LL caused a loss of rhythmicity and a reduction in the immunopositive cells of VIP, AVP, and PER1 in the suprachiasmatic nucleus (SCN). In the short term, the affection on the circadian clock in the pups resulted in body weight gain, loss of daily rhythms in general activity, plasma glucose and triglycerides (TG). Importantly, the DD conditions during development also induced altered daily rhythms in general activity and in the SCN. Exposure to LD conditions after lactation did not restore rhythmicity in the SCN, and the number of immunopositve cells to VIP, AVP, and PER1 remained reduced. In the long term, daily rhythmicity in general activity was restored; however, daily rhythms in glucose and TG remained disrupted, and daily mean levels of TG were significantly increased. Present results point out the programming role played by the LD cycle during early development in the function of the circadian system and on metabolism. This study points out the risk represented by exposure to an altered light-dark cycle during early stages of development.
AVP: arginine vasopressin peptide; CRY: cryptochrome; DD: constant darkness; DM: dorsomedial; LD: light-dark cycle; LL: constant light; NICUs: neonatal intensive care units; P: postnatal days; PER: period; S.E.M.: standard error of the mean; SCN: suprachiasmatic nucleus; TG: triglycerides; VIP: vasointestinal peptide; VL: ventrolateral; ZT: zeitgeber time.
夜间光照对成年生物钟系统是一种干扰性条件,会导致夜间啮齿动物出现节律紊乱。生物钟紊乱是引发生理和行为改变(包括体重增加和代谢疾病)的一个风险因素。在发育早期阶段,生物钟系统会经历一个关键的调整期,并且特别容易受到可能对其功能进行编程的光照条件改变的影响,从而导致长期影响。我们推测在哺乳期,夜间光照导致的昼夜明暗周期紊乱可能会扰乱生物钟系统,并长期诱发代谢紊乱。在此,我们探究了哺乳期持续光照(LL)对幼崽的短期和长期影响。短期内,LL导致视交叉上核(SCN)中VIP、AVP和PER1的免疫阳性细胞节律丧失和减少。短期内,对幼崽生物钟的影响导致体重增加、一般活动、血浆葡萄糖和甘油三酯(TG)的昼夜节律丧失。重要的是,发育期间的持续黑暗(DD)条件也会导致一般活动和SCN中的昼夜节律改变。哺乳期后暴露于昼夜明暗(LD)条件下并不能恢复SCN中的节律,并且VIP、AVP和PER1的免疫阳性细胞数量仍然减少。从长期来看,一般活动的昼夜节律得以恢复;然而,葡萄糖和TG的昼夜节律仍然紊乱,并且TG的日平均水平显著升高。目前的结果指出了昼夜明暗周期在早期发育过程中对生物钟系统功能和新陈代谢所起的编程作用。这项研究指出了发育早期阶段暴露于改变的昼夜明暗周期所代表的风险。
AVP:精氨酸加压素肽;CRY:隐花色素;DD:持续黑暗;DM:背内侧;LD:昼夜明暗周期;LL:持续光照;NICUs:新生儿重症监护病房;P:出生后天数;PER:周期;S.E.M.:平均值的标准误差;SCN:视交叉上核;TG:甘油三酯;VIP:血管活性肠肽;VL:腹外侧;ZT:授时因子时间