Denigma cartographies changes from the molecular level to whole physiology which occur in defined contrasts such as aging and dietary as well as genetic lifespan-extending interventions:
ID | name | taxid | reference | pmid | tissue | comparision | start | stop | gender | description |
---|---|---|---|---|---|---|---|---|---|---|
72 | IGF2 level changes | 9606 | — | 3322823 | plasma | age | — | — | — | Circulating IGF2 reaches âadultâ levels early in childhood, and changes are relatively small as a function of increasing age [3322823]. |
54 | DHEA decreases | 9544 | Lane et al., 1997 | 9215277 | serum | Age | 5 year | 26 year | males/females | Males and female rhesus monkeys exhibit a steady, age-related decline in serum DHEAS. The proportional age-related loss of DHEAS in rhesus moneys is over twice the rate of decline observed in humans [9215277]. |
55 | DHEA deline slows | 9544 | Lane et al., 199 | 9215277 | serum | diet | DR | — | males/females | DR slows postmaturational decline in serum DHEAS levels form the age of 6.5 to 9.5 [9215277]. |
52 | DHEA decreases | 9606 | Hinson and Raven, 1999 | 10495400 | serum | age | 25 year | 85 year | males/females | DHEAS (Dehydroepiandrosterone sulphate) is the most abundant circulating steroid secreted by adrenal glands. Duo to its position int the steroid cascade DHEA act like kind of âthe mother steroidâ (Regelson et al., 1994). DHEA reaches its highest levels at age 20-24. Its serum concentration declines with increasing age after 25 years and diminishes about 95% by 85 years. DHEA deficiency syndrome is a new term for old age [10495400]. |
53 | DHEA increases | 9606 | Hinson and Raven, 1999 | 10495400 | serum | age | 10 year | 20 year | males/females | DHEA reaches its highest levels at age 20-24 [10495400]. |
1 | ROS production increases | 4932 | Laun et al., 2001 | 11251834 | — | Age | young | old | — | — |
85 | Cell proliferation decreases | 10116 | — | 11744049 | — | Diet | — | — | — | 24 month DR in rats inhibits cell proliferation in glandular stomach and liver tissue [11744049]. |
41 | Mitochondrial dysfunction increases | 9606 | Petersen et al., 2003 | 12750520 | muscle | Age | — | — | — | Aging is accompanied by an increase in mitochondrial dysfunction in muscle of humans [12750520]. |
67 | Bone loss | 10090 | — | 13678781 | bone | age | 42 week | 104 week | male | In young mice the rapid growth is marked by substantial increase in bone size, mineral mass and mechanical properties. Maturation occurring between 12 and 42 weeks of age was characterized with the maintenance of bone mass and mechanical properties. From the peak levels, mice aged for 104 weeks exhibited decreased whole femur mass, percentage of mineralization diminished whole bone stiffness, energy to fracture and decreased cortical thickness. Periosteal perimeter and, consequently the cross-sectional moments of inertia continued to increase through 104 weeks, compensating for cortical thinning and increased brittleness due to decreased mineralization and stiffness. The shape of the mid-diaphysis became increasingly less elliptical in aged mice. After 52 weeks excessive endocortical resorption appeared, indicating a shift in normal mechanisms regulating bone shape and locating, suggestive of remodelling [13678781]. |
38 | HDL increases | 9606 | Fontana et al., 2004 | 15096581 | Plasma | Diet | Chronic DR | — | — | — |
39 | AMP/ATP increases | 6239 | Apfeld et al., 2004 | 15574588 | whole body | Age | 4 day | 18 day | Hemaphrodite | AMP/ATP ratio in living animals increases from <0.1 at day 4 of adulthood to 0.8 at day 18 (an age near the maximum lifespan of the population). Linear regression indicates a strong correlation between AMP/ATP ratio and life expectancy. |
40 | Accumulation of lipofuscin-like fluorescent pigment | 6239 | Apfeld et al., 2004 | 15574588 | intestine | Age | 1 day | 7 day | Hemaphrodite | A lipofuscin-like fluorescent pigment accumulates in an age-dependent manner in the intestine (Garigan et al., 2002; Herndon et al., 2002). It accumulates at a faster rate in aak-2 mutant, which have a shortened lifespan [15574588]. |
81 | elt-5 expression increases | 6239 | 17608836 | 17608836 | — | age | — | — | — | Expression of elt-5 increases with during devleopment and aging [17608836]. |
82 | elt-6 expression increases | 6239 | — | 17608836 | — | age | — | — | — | Expression of elt-6 increases during devleopment and aging [17608836]. |
83 | elt-3 expression increases | 6239 | — | 17608836 | — | age | — | — | — | Expression of elt-3 increases during devleopment and aging [17608836]. |
51 | DHEA increases | 9606 | Willcox et al., 2007 | 17986602 | serum | diet | Okinawa | — | — | Okinawa aged 65-plus have relatively high DHEA levels. |
124 | Reduced expression of autophagy genes | 7227 | — | 18059160 | neural | age | old | young | — | The expression of several autophagy genes is reduced in neural tissues as a normal part of aging [18059160]. |
125 | Insoluble ubiquitinated proteins accumulate | 7227 | — | 18059160 | neuronal | age | old | young | — | Insoluble ubiquitinated proteins, markers of neuronal aging and degeneration, accumulate with aging in concomitantly with the age-dependent suppression of autopagy [18059160]. |
130 | Melatonin decreases | — | — | 18212404 | — | age | old | young | — | Melatonin level decrease with age [reviewed in 18212404]. |
79 | Vacuolar membrane deteriorates | 4932 | — | 18690010 | — | age | — | — | — | The vacuolar membrane deteriorates as judged by Vac8 localisation at or before generations 6-7. At generation 6-7, cells begin to exhibit large round vacoules and vacoules with invaginated vacoular membranes [18690010]. |
69 | Loss of subcutaneous adipose skin layer | 10090 | — | 19013273 | skin | age | 5 | 165 | — | With increasing age the subcutaneous adipose layer becomes thinner (5-12 weeks vs. 123-165 weeks) and this loss is associated with increased risk of skin injuries and infections [19013273]. |
101 | Enhanced mitochondrial function | 7227 | Zid et al. 2009 | 19804760 | — | diet | DR | AL | — | Flies upon DR have enhanced mitochondrial function, which is mediated by enhanced mRNA translation of nuclear-encoded mitochondrial mRNAs in a d4E-BP dependent manner [19804760] |
62 | Fertility declines | 6239 | — | 20041217 | whole body | age | — | — | females | Fertility and reproduction sharply decline in early/mide-adulthood, folloed by a long post-reproductuve period, followed by a long-post-reproductive period [6,7 in 20041217]. |
2 | Downregulation of exo-3 | 6239 | Schlotterer et al., 2010 | 20346071 | Whole body | Age | — | — | — | — |
103 | Decreased stem cell activity | — | — | 20504968 | — | age | — | — | — | Advanced age is associated with decreased stem cell activity [20504968]. |
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