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全球有8億人飽受肥胖困擾,預(yù)計(jì)到2025年,肥胖相關(guān)醫(yī)療費(fèi)用將超過(guò)1萬(wàn)億美元。根據(jù)美國(guó)疾病控制與預(yù)防中心數(shù)據(jù),超過(guò)40%的美國(guó)人口受此影響。肥胖是糖尿病、胰島素抵抗、高血壓等代謝性疾病的主要風(fēng)險(xiǎn)因素。

長(zhǎng)期晝夜節(jié)律紊亂(調(diào)控人體大部分活動(dòng)的24小時(shí)生物鐘)與肥胖、糖耐量受損及2型糖尿病等多種疾病密切相關(guān)。晝夜節(jié)律幾乎與所有代謝過(guò)程及能量穩(wěn)態(tài)存在雙向交互作用1。最新研究表明,晝夜節(jié)律通過(guò)調(diào)控代謝相關(guān)酶、激素及轉(zhuǎn)運(yùn)系統(tǒng)的周期性表達(dá)與活性,控制能量穩(wěn)態(tài)?。
主時(shí)鐘與外圍時(shí)鐘
晝夜節(jié)律是與生俱來(lái)的24小時(shí)周期,影響睡眠-覺(jué)醒周期等行為及生理過(guò)程,幫助生物體預(yù)測(cè)并適應(yīng)環(huán)境變化。? 其核心調(diào)控中樞位于下丘腦的視交叉上核(SCN),作為主時(shí)鐘,SCN同步調(diào)控肝臟、肌肉、腸道、心臟及胰腺等外周組織的局部時(shí)鐘。?? 中央與局部晝夜節(jié)律系統(tǒng)形成反饋環(huán)路,共同調(diào)節(jié)能量穩(wěn)態(tài)、激素分泌、心血管健康及體溫等關(guān)鍵功能,SCN是該環(huán)路的核心同步器。
SCN需依賴(lài)外界光暗周期每日重置,以使生物節(jié)律與環(huán)境同步。這一過(guò)程依賴(lài)多種外部信號(hào)(稱(chēng)為“授時(shí)因子”,德語(yǔ)“zeitgeber”意為“時(shí)間給予者”?),包括光照、溫度、進(jìn)食時(shí)間及運(yùn)動(dòng)等。晝夜節(jié)律可能因晚食、夜班、跨時(shí)區(qū)旅行或藥物攝入等因素失調(diào)。當(dāng)生物鐘協(xié)調(diào)時(shí),人體日間攝食、胃腸活動(dòng)及代謝功能增強(qiáng),夜間則減弱以準(zhǔn)備睡眠。? 一旦中樞或外周節(jié)律失調(diào),便可能引發(fā)健康問(wèn)題。

成千上萬(wàn)的生物鐘形成了一個(gè)反饋回路,調(diào)節(jié)著能量穩(wěn)態(tài)等生理過(guò)程。
中樞時(shí)鐘失調(diào)與肥胖
對(duì)中樞時(shí)鐘而言,光照是最重要的觸發(fā)因素。自然光線(xiàn)減弱時(shí),褪黑素分泌增加。褪黑素通過(guò)調(diào)節(jié)中樞及外周節(jié)律相關(guān)基因表達(dá),維持代謝與激素平衡。? 例如,在脂肪組織中,褪黑素通過(guò)調(diào)控碳水化合物與脂質(zhì)代謝相關(guān)基因的節(jié)律性表達(dá),同步代謝與激素功能。? 夜間人工光源等干擾會(huì)破壞中樞時(shí)鐘,抑制褪黑素分泌,導(dǎo)致睡眠問(wèn)題,進(jìn)而改變代謝等外周過(guò)程的節(jié)律。

睡眠不足不僅會(huì)導(dǎo)致吃更多的食物,而且還會(huì)選擇高熱量的食物。
長(zhǎng)期睡眠不足引發(fā)的晝夜節(jié)律紊亂與過(guò)度進(jìn)食及肥胖風(fēng)險(xiǎn)增加密切相關(guān)。?? 研究表明,睡眠限制會(huì)改變饑餓素(ghrelin)與瘦素(leptin)水平,促使個(gè)體攝入更多熱量。饑餓素(促進(jìn)食欲)水平升高,而瘦素(產(chǎn)生飽腹感)水平下降。??
威斯康星睡眠隊(duì)列研究發(fā)現(xiàn),每日僅5小時(shí)睡眠者,晨間瘦素水平降低15%,饑餓素水平升高相似幅度。?? 另一項(xiàng)研究顯示,連續(xù)四晚僅睡4.5小時(shí)的受試者在自助餐中熱量攝入增加14%,且更傾向于選擇高碳水化合物食物。?? 這些結(jié)果表明,短睡眠周期不僅增加進(jìn)食量,還會(huì)促使高熱量食物的選擇,更易導(dǎo)致脂肪堆積。
外周時(shí)鐘失調(diào)與肥胖
人體內(nèi)數(shù)千個(gè)外周時(shí)鐘分布于心臟、胰腺及肝臟等器官,持續(xù)與SCN重新同步。?? 不同于中樞時(shí)鐘依賴(lài)光照,外周時(shí)鐘的主要授時(shí)因子是禁食與進(jìn)食時(shí)間。?? 盡管無(wú)法直接在人類(lèi)中誘導(dǎo)肥胖研究,科學(xué)家通過(guò)動(dòng)物模型揭示了進(jìn)食時(shí)間對(duì)體重的影響。例如,在小鼠正常休息時(shí)段喂食會(huì)擾亂外周時(shí)鐘,導(dǎo)致暴食、瘦素抵抗、體力活動(dòng)減少、肝臟脂肪堆積及肥胖。??
為探究晝夜節(jié)律基因的重要性,研究者敲除或突變小鼠的特定節(jié)律基因,發(fā)現(xiàn)突變小鼠因暴食導(dǎo)致脂肪量較正常小鼠增加35%。?? 這些研究證實(shí),外周節(jié)律失調(diào)會(huì)引發(fā)系統(tǒng)性改變,最終導(dǎo)致肥胖。
授時(shí)因子對(duì)生物鐘及代謝的影響
授時(shí)因子 | 授時(shí)因子 |
晝夜節(jié)律紊亂(輪班、時(shí)差、睡眠障礙) | 糖脂代謝異常、胰島素敏感性↓、炎癥↑、心血管疾病風(fēng)險(xiǎn)↑ |
進(jìn)食模式(早食、間歇性禁食、限時(shí)進(jìn)食) | 血糖、胰島素、GLP-1、甘油三酯、BMI、血壓、體重、β細(xì)胞反應(yīng)性、氧化應(yīng)激、脂肪氧化及膽固醇水平波動(dòng) |
體力活動(dòng)(定時(shí)運(yùn)動(dòng)) | 耗氧量、呼吸交換率、心率、血糖水平及體溫變化 |
改編自Guan和Lazar??
時(shí)間即關(guān)鍵:探索晝夜節(jié)律干預(yù)與療法
研究者通過(guò)解析晝夜節(jié)律與代謝疾病的關(guān)聯(lián),開(kāi)發(fā)潛在干預(yù)手段。運(yùn)動(dòng)、藥物及進(jìn)食時(shí)間等授時(shí)因子是明確的研究目標(biāo),旨在探索其時(shí)間調(diào)控對(duì)健康的影響。

- 時(shí)間運(yùn)動(dòng)學(xué)(Chronoexercise):根據(jù)個(gè)體晝夜節(jié)律優(yōu)化運(yùn)動(dòng)時(shí)間與時(shí)長(zhǎng),以改善代謝疾病及胰島素敏感性。??
- 時(shí)間藥理學(xué)(Chronopharmacology):確定藥物最佳服用時(shí)間以提升療效。?? 例如,通過(guò)檢測(cè)個(gè)體的褪黑素分泌曲線(xiàn)確定“暗光褪黑素起始時(shí)間(DLMO)”,指導(dǎo)治療時(shí)機(jī)。
- 限時(shí)進(jìn)食:動(dòng)物研究表明,熱量限制與間歇性禁食可能通過(guò)提供時(shí)間信號(hào)重置生物鐘,改善代謝健康。??
總結(jié)
肥胖是一種由多通路介導(dǎo)的復(fù)雜疾病。?? 中樞時(shí)鐘(如光污染、睡眠不足)或外周時(shí)鐘(如進(jìn)食時(shí)間紊亂)的直接干擾會(huì)引發(fā)激素分泌與生理過(guò)程的級(jí)聯(lián)效應(yīng),導(dǎo)致暴食及代謝異常,最終增加肥胖風(fēng)險(xiǎn)。通過(guò)尊重生物節(jié)律的固定作息(如定時(shí)運(yùn)動(dòng)、進(jìn)食及用藥),可正向調(diào)控晝夜節(jié)律及其相關(guān)生理過(guò)程。時(shí)間運(yùn)動(dòng)學(xué)與時(shí)間藥理學(xué)等新興領(lǐng)域正探索如何將外部活動(dòng)與生物鐘對(duì)齊,以最大化健康效益。
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檢測(cè)指標(biāo) | 產(chǎn)品貨號(hào) | 產(chǎn)品名稱(chēng) | 規(guī)格 |
胰島素原 | ALP-82-PINHUI-E01 | Intact Proinsulin ELISA | 96 Wells |
ALP-82-PINHUT-E01 | Total Proinsulin ELISA | 96 Wells | |
胰島素 | ALP-80-INSHU-E01.1 | Insulin ELISA | 96 Wells |
ALP-80-INSHU-E10.1 | Insulin ELISA Jumbo Pack (10 Plates) | 10 x 96 Wells | |
ALP-80-INSHUU-E01.1 | Insulin Ultrasensitive EIA (96 Wells), "IVD" | 96 Wells | |
ALP-80-INSHUU-E10 | Ultrasensitive Insulin ELISA Jumbo Pack (10 Plates) | 10 x 96 Wells | |
ALP-80-INSMS-E01 | Mouse Insulin ELISA | 96 Wells | |
ALP-80-INSMS-E10 | Mouse Insulin ELISA Jumbo Pack (10 Plates) | 10 x 96 Wells | |
ALP-80-INSMSH-E01 | Mouse High Range Insulin ELISA | 96 Wells | |
ALP-80-INSMSU-E01 | Mouse Ultrasensitive Insulin ELISA | 96 Wells | |
ALP-80-INSMSU-E10 | Mouse Ultrasensitive Insulin ELISA Jumbo Pack (10 Plates) | 10 x 96 Wells | |
ALP-80-INSRT-E01 | Rat Insulin ELISA | 96 Wells | |
ALP-80-INSRT-E10 | Rat Insulin ELISA Jumbo Pack (10 Plates) | 10 x 96 Wells | |
ALP-80-INSRTH-E01 | Rat High Range Insulin ELISA | 96 Wells | |
ALP-80-INSRTU-E01 | Insulin (Rat) Ultrasensitive, 96w, "RUO" | 96 Wells | |
ALP-80-INSMR-CH01 | Rodent Insulin Chemiluminescence ELISA | 96 Wells | |
ALP-80-INSMR-CH10 | Rodent Insulin Chemiluminescence ELISA Jumbo Pack (10 Plates) | 10 x 96 Wells | |
ALP-80-INSBO-E01 | Bovine Insulin ELISA | 96 Wells | |
ALP-80-INSHU-CH01 | Insulin Chemiluminescence ELISA | 96 Wells | |
ALP-80-INSHU-CH10 | Insulin Chemiluminescence ELISA Jumbo Pack (10 Plates) | 10 x 96 Wells | |
C-肽 | ALP-80-CPTHU-E01.1 | C-Peptide ELISA | 96 Wells |
ALP-80-CPTHU-E10 | C-Peptide ELISA Jumbo Pack (10 Plates) | 10 x 96 Wells | |
ALP-80-CPTMS-E01 | C-Peptide (Mouse) ELISA, 96 wells, "RUO" | 96 Wells | |
ALP-80-CPTRT-E01 | C-Peptide (Rat) ELISA, 96 wells, "RUO" | 96 Wells | |
ALP-80-CPTHU-CH01 | C-Peptide Chemiluminescence ELISA | 96 Wells | |
ALP-80-CPTHU-CH05 | C-Peptide Chemiluminescence ELISA Lab Pack (5 Plates) | 5 x 96 Wells | |
胰高血糖素 | ALP-11-GLUHU-E01 | Glucagon ELISA | 96 Wells |
ALP-48-GLUHUU-E01 | Glucagon Ultrasensitive EIA, 96w, "RUO" | 96 Wells | |
脂聯(lián)素 | ALP-22-ADPMS-E01 | Mouse Total Adiponectin ELISA, 96-wells, RUO | 96 Wells |
ALP-22-ADPRT-E01 | Adiponectin (Rat) ELISA, 96 wells, "RUO" | 96 Wells | |
ALP-80-ADPHU-E01 | Human HMW &Total Adiponectin ELISA, 96 wells, "RUO" | 96 Wells | |
瘦素 | ALP-11-LEPHU-E01 | Leptin ELISA "RUO" | 96 Wells |
ALP-22-BLEPHU-E01 | Bioactive Leptin ELISA | 96 Wells | |
ALP-22-LEPHUU-E01 | Leptin Ultrasensitive ELISA, 96 wells, "RUO" | 96 Wells | |
ALP-22-LEPMS-E01 | Mouse/Rat Leptin EIA (96 wells), "RUO" | 96 Wells | |
GIP | ALP-48-AGIPHU-E01 | Active GIP ELISA | 96 Wells |
ALP-48-AGIPMS-E01 | Mouse Active GIP ELISA | 96 Wells | |
ALP-48-AGIPRT-E01 | Rat Active GIP ELISA | 96 Wells | |
ALP-48-GIPHU-E01 | Total GIP ELISA | 96 Wells | |
ALP-48-GIPMS-E01 | Mouse Total GIP ELISA | 96 Wells | |
ALP-48-GIPRT-E01 | Rat Total GIP ELISA | 96 Wells | |
GLP-1 | ALP-43-GP1HU-E01 | GLP-1 (Active 7-36) ELISA, 96 wells "RUO" | 96 Wells |
ALP-43-GPTHU-E01 | GLP-1 (7-36 and 9-36) ELISA, 96 wells | 96 Wells | |
ALP-80-GLP1A-CH01 | Active GLP-1 (7-36) amide Chemiluminescence ELISA | 96 Wells | |
GLP-2 | ALP-48-GP2HU-E01.1 | GLP-2 EIA "RUO" | 96 Wells |
ALP-48-GP2MS-E01 | GLP-2 (Mouse) EIA "RUO" | 96 Wells | |
ALP-48-GP2RT-E01 | GLP-2 (Rat) EIA "RUO" | 96 Wells | |
PYY | ALP-48-PYYHU-E01.1 | PYY EIA, "RUO" | 96 Wells |
ALP-48-PYYRT-E01.1 | PYY (Rat) EIA "RUO" | 96 Wells |
參考文獻(xiàn)
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