Wissenschaftliche Referenzen: Mikrohacks – Hormone, Zellenergie & Longevity
Hormone, Zellenergie & Longevity.
Die Quellen zu jeder Karte.
Dieses Verzeichnis dokumentiert die Fachliteratur, auf die sich die Karten dieses Decks stützen. Es ist nach Kartenthemen geordnet: Zu jedem Thema finden Sie die zugehörigen Publikationen mit direktem Link zur Originalquelle. Relevante inhaltliche Aussagen sollen auf überprüfbare, in Fachzeitschriften begutachtete Arbeiten zurückführbar sein. Allgemein bekannte Aussagen werden hier nicht belegt.
Die aufgeführten Quellen dienen der wissenschaftlichen Einordnung und der Nachvollziehbarkeit. Sie stellen keine medizinische Beratung dar und ersetzen nicht das Gespräch mit Ärztin oder Arzt. Die Nennung einer Studie ist keine Heil- oder Wirkungsaussage.
Stand: August 2026 · 149 Quellenangaben
Wichtigste Grundlagen
Themen: empfohlener Bewegungsumfang, Schlafdauer, soziale Einbindung, Lebenssinn, Ernährungsqualität, Rolle der Mitochondrien.
Bull, F. C., et al. (2020). World Health Organization 2020 guidelines on physical activity and sedentary behaviour. British Journal of Sports Medicine, 54(24), 1451–1462.
Shailendra, P., et al. (2022). Resistance training and mortality risk: a systematic review and meta-analysis. American Journal of Preventive Medicine, 63(2), 277–285.
Hirshkowitz, M., et al. (2015). National Sleep Foundation's updated sleep duration recommendations. Sleep Health, 1(4), 233–243. https://doi.org/10.1016/j.sleh.2015.10.004
Holt-Lunstad, J., et al. (2015). Loneliness and social isolation as risk factors for mortality. Perspectives on Psychological Science, 10(2), 227–237. https://doi.org/10.1177/1745691614568352
Holt-Lunstad, J., et al. (2010). Social relationships and mortality risk. PLOS Medicine, 7(7), e1000316. https://doi.org/10.1371/journal.pmed.1000316
Cohen, R., et al. (2016). Purpose in life and its relationship to all-cause mortality and cardiovascular events. Psychosomatic Medicine, 78(2), 122–133. https://doi.org/10.1097/PSY.0000000000000274
Lane, M. M., et al. (2024). Ultra-processed food exposure and adverse health outcomes. BMJ, 384, e077310. https://doi.org/10.1136/bmj-2023-077310
Barbaresko, J., et al. (2024). Ultra-processed food consumption and human health. Critical Reviews in Food Science and Nutrition, 65(11), 1999–2007. https://doi.org/10.1080/10408398.2024.2317877
Brand, M. D., et al. (2013). The role of mitochondrial function and cellular bioenergetics in ageing and disease. British Journal of Dermatology, 169(Suppl. 2), 1–8. https://doi.org/10.1111/bjd.12208
Lanza, I. R., et al. (2010). Mitochondrial function as a determinant of life span. Pflügers Archiv – European Journal of Physiology, 459(2), 277–289.
↑ Zum VerzeichnisBiologische Steuerung
Themen: Allostase und Ressourcenpriorisierung unter Belastung, niedriggradige chronische Entzündung, Omega-3 und Zellmembranfunktion.
McEwen, B. S., et al. (2003). The concept of allostasis in biology and biomedicine. Hormones and Behavior, 43(1), 2–15. https://doi.org/10.1016/S0018-506X(02)00024-7
Chrousos, G. P. (2009). Stress and disorders of the stress system. Nature Reviews Endocrinology, 5(7), 374–381. https://doi.org/10.1038/nrendo.2009.106
Franceschi, C., et al. (2014). Chronic inflammation (inflammaging) and its potential contribution to age-associated diseases. The Journals of Gerontology: Series A, 69(Suppl. 1), S4–S9. https://doi.org/10.1093/gerona/glu057
Liao, Y., et al. (2022). Possible antidepressant mechanisms of omega-3 polyunsaturated fatty acids acting on the central nervous system. Frontiers in Psychiatry, 13, 933704. https://doi.org/10.3389/fpsyt.2022.933704
↑ Zum VerzeichnisCholecalciferol (Sonnenhormon & Gen-Regulator)
Themen: VDR und Genregulation, breitengrad- und saisonabhängiger Bedarf, DGE- und EFSA-Richtwerte, Magnesium als Kofaktor, Vitamin K2 und Kalziumverteilung.
Bouillon, R., et al. (2019). Skeletal and extraskeletal actions of vitamin D. Endocrine Reviews, 40(4), 1109–1151. https://doi.org/10.1210/er.2018-00126
Zmijewski, M. A. (2019). Vitamin D and human health. International Journal of Molecular Sciences, 20(1), 145. https://doi.org/10.3390/ijms20010145
Cashman, K. D., et al. (2008). Estimation of the dietary requirement for vitamin D in healthy adults. The American Journal of Clinical Nutrition, 88(6), 1535–1542. https://doi.org/10.3945/ajcn.2008.26594
EFSA Panel on Dietetic Products, Nutrition and Allergies. (2012). Scientific opinion on the tolerable upper intake level of vitamin D. EFSA Journal, 10(7), 2813. https://doi.org/10.2903/j.efsa.2012.2813
Uwitonze, A. M., et al. (2018). Role of magnesium in vitamin D activation and function. Journal of the American Osteopathic Association, 118(3), 181–189. https://doi.org/10.7556/jaoa.2018.037
Schurgers, L. J., et al. (2008). Matrix Gla-protein: the calcification inhibitor in need of vitamin K. Thrombosis and Haemostasis, 100(4), 593–603. https://doi.org/10.1160/TH08-02-0087
↑ Zum VerzeichnisSchilddrüsenhormone (Stoffwechsel-Taktgeber)
Themen: Schilddrüsenhormone im Energiestoffwechsel, T4-zu-T3-Umwandlung und reverse T3, Schilddrüse und Lipidstoffwechsel, Ferritin und Schilddrüsenfunktion.
Mullur, R., et al. (2014). Thyroid hormone regulation of metabolism. Physiological Reviews, 94(2), 355–382. https://doi.org/10.1152/physrev.00030.2013
Warner, M. H., et al. (2010). Mechanisms behind the non-thyroidal illness syndrome: an update. Journal of Endocrinology, 205(1), 1–13. https://doi.org/10.1677/JOE-09-0412
Liu, H., et al. (2022). Update on dyslipidemia in hypothyroidism. Endocrine Connections, 11(2), e210002. https://doi.org/10.1530/EC-21-0002
Shin, D.-J., et al. (2003). Thyroid hormone regulation and cholesterol metabolism connected through SREBP-2. Journal of Biological Chemistry, 278(36), 34114–34118. https://doi.org/10.1074/jbc.M305417200
Soriguer, F., et al. (2011). Iron deficiency is associated with hypothyroxinemia and hypotriiodothyroninemia (Di@bet.es study). https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919900/
Garofalo, V., et al. (2023). Relationship between iron deficiency and thyroid function: a systematic review and meta-analysis. Nutrients, 15(22), 4790. https://doi.org/10.3390/nu15224790
↑ Zum VerzeichnisInsulin (Energieverteilung & Fettspeicherung)
Themen: Insulinwirkung und Insulinresistenz, Essig und postprandiale Glukoseantwort, HOMA-IR als Messgröße.
Petersen, M. C., et al. (2018). Mechanisms of insulin action and insulin resistance. Physiological Reviews, 98(4), 2133–2223. https://doi.org/10.1152/physrev.00063.2017
Shishehbor, F., et al. (2017). Vinegar consumption can attenuate postprandial glucose and insulin responses. Diabetes Research and Clinical Practice, 127, 1–9. https://doi.org/10.1016/j.diabres.2017.01.021
Matthews, D. R., et al. (1985). Homeostasis model assessment: insulin resistance and β-cell function. Diabetologia, 28(7), 412–419. https://doi.org/10.1007/BF00280883
Tang, Q., et al. (2015). Optimal cut-off values for the HOMA-IR and the metabolic syndrome. Drug Discoveries & Therapeutics, 9(6), 380–385. https://doi.org/10.5582/ddt.2015.01207
↑ Zum VerzeichnisCortisol (Dauerstress & Energiebereitstellung)
Themen: zirkadianer Cortisol-Rhythmus und Cortisol Awakening Response, Folgen chronischer Belastung, Vitamin C in der Nebenniere, langsame Atmung und Parasympathikus.
Adam, E. K., et al. (2017). Diurnal cortisol slopes and mental and physical health outcomes. Psychoneuroendocrinology, 83, 25–41. https://doi.org/10.1016/j.psyneuen.2017.05.018
Clow, A., et al. (2010). The cortisol awakening response: more than a measure of HPA axis function. Neuroscience & Biobehavioral Reviews, 35(1), 97–103. https://doi.org/10.1016/j.neubiorev.2009.12.011
Chrousos, G. P. (2009). Stress and disorders of the stress system. Nature Reviews Endocrinology, 5(7), 374–381. https://doi.org/10.1038/nrendo.2009.106
Patak, P., et al. (2009). Vitamin C is an important cofactor for both adrenal cortex and adrenal medulla. Endocrine Research, 30(4), 871–875. https://doi.org/10.1081/ERC-200044126
Zaccaro, A., et al. (2018). How breath-control can change your life: a systematic review on psychophysiological correlates of slow breathing. Frontiers in Human Neuroscience, 12, 353. https://doi.org/10.3389/fnhum.2018.00353
↑ Zum VerzeichnisAdrenalin (Akut-Alarm & Kampf/Flucht)
Themen: Akut-Stressreaktion auf psychosoziale Reize, Tauchreflex und Herzfrequenz, kognitive Neubewertung (Reappraisal), langsame Ausatmung.
Chrousos, G. P. (2009). Stress and disorders of the stress system. Nature Reviews Endocrinology, 5(7), 374–381. https://doi.org/10.1038/nrendo.2009.106
Panneton, W. M. (2013). The mammalian diving response: an enigmatic reflex to preserve life? Physiology, 28(5), 284–297. https://doi.org/10.1152/physiol.00020.2013
Brooks, A. W. (2014). Get excited: reappraising pre-performance anxiety as excitement. Journal of Experimental Psychology: General, 143(3), 1144–1158. https://doi.org/10.1037/a0035325
Zaccaro, A., et al. (2018). How breath-control can change your life. Frontiers in Human Neuroscience, 12, 353. https://doi.org/10.3389/fnhum.2018.00353
↑ Zum VerzeichnisDopamin (Antrieb & Zielverfolgung)
Themen: Belohnungssystem und Rezeptorsensitivität, Belohnungsvorhersage und Teilziele, körperliche Aktivität, Kältereiz.
Volkow, N. D., et al. (2017). The dopamine motive system: implications for drug and food addiction. Nature Reviews Neuroscience, 18(12), 741–752. https://doi.org/10.1038/nrn.2017.130
Schultz, W. (1998). Predictive reward signal of dopamine neurons. Journal of Neurophysiology, 80(1), 1–27. https://doi.org/10.1152/jn.1998.80.1.1
Marques, A., et al. (2021). Bidirectional association between physical activity and dopamine across adulthood. Brain Sciences, 11(7), 829. https://doi.org/10.3390/brainsci11070829
Šramek, P., et al. (2000). Human physiological responses to immersion into water of different temperatures. European Journal of Applied Physiology, 81(5), 436–442. https://doi.org/10.1007/s004210050065
↑ Zum VerzeichnisNoradrenalin (Wachheit & Fokus)
Themen: Locus-coeruleus-Aktivität und Aufmerksamkeit (umgekehrte U-Kurve), Tageslicht und Aktivierung, Kältereiz.
Aston-Jones, G., et al. (2005). An integrative theory of locus coeruleus–norepinephrine function. Annual Review of Neuroscience, 28, 403–450. https://doi.org/10.1146/annurev.neuro.28.061604.135709
Blume, C., et al. (2019). Effects of light on human circadian rhythms, sleep and mood. Somnologie, 23(3), 147–156. https://doi.org/10.1007/s11818-019-00215-x
Šramek, P., et al. (2000). Human physiological responses to immersion into water of different temperatures. European Journal of Applied Physiology, 81(5), 436–442. https://doi.org/10.1007/s004210050065
↑ Zum VerzeichnisAcetylcholin (Lernen & Gedächtnis)
Themen: Aufmerksamkeit, Enkodierung und Neuroplastizität, Signal-Rausch-Modulation, Gedächtniskonsolidierung im Schlaf, anticholinerge Substanzen.
Hasselmo, M. E. (2006). The role of acetylcholine in learning and memory. Current Opinion in Neurobiology, 16(6), 710–715. https://doi.org/10.1016/j.conb.2006.09.002
Hasselmo, M. E., et al. (2004). High acetylcholine levels set circuit dynamics for attention and encoding. Progress in Brain Research, 145, 207–231. https://doi.org/10.1016/S0079-6123(03)45015-2
Hasselmo, M. E. (1999). Neuromodulation: acetylcholine and memory consolidation. Trends in Cognitive Sciences, 3(9), 351–359. https://doi.org/10.1016/S1364-6613(99)01365-0
Risacher, S. L., et al. (2016). Association between anticholinergic medication use and cognition, brain metabolism, and brain atrophy. JAMA Neurology, 73(6), 721–732. https://doi.org/10.1001/jamaneurol.2016.0580
↑ Zum VerzeichnisGABA (Reizfilter & innere Ruhe)
Themen: GABA als hemmender Neurotransmitter, Vitamin B6 in der GABA-Synthese, Magnesium und NMDA-Modulation, L-Theanin und Alpha-Aktivität, Alkohol und GABA-Rezeptoren.
Petroff, O. A. C. (2002). GABA and glutamate in the human brain. The Neuroscientist, 8(6), 562–573. https://doi.org/10.1177/1073858402238515
Calderón-Ospina, C. A., et al. (2020). B vitamins in the nervous system. CNS Neuroscience & Therapeutics, 26(1), 5–13. https://doi.org/10.1111/cns.13207
Kirkland, A. E., et al. (2018). The role of magnesium in neurological disorders. Nutrients, 10(6), 730. https://doi.org/10.3390/nu10060730
Nobre, A. C., et al. (2008). L-theanine, a natural constituent in tea, and its effect on mental state. Asia Pacific Journal of Clinical Nutrition, 17(Suppl. 1), 167–168. https://pubmed.ncbi.nlm.nih.gov/18296328/
Davies, M. (2003). The role of GABA-A receptors in mediating the effects of alcohol in the central nervous system. Journal of Psychiatry & Neuroscience, 28(4), 263–274. https://pmc.ncbi.nlm.nih.gov/articles/PMC165791/
↑ Zum VerzeichnisSerotonin (Zufriedenheit & innere Stabilität)
Themen: enterale Serotoninproduktion und getrennte Pools, Mikrobiom und kurzkettige Fettsäuren, Tryptophan-Transport ins Gehirn, Kynureninpfad, Omega-3 und Stimmung.
El-Merahbi, R., et al. (2015). The roles of peripheral serotonin in metabolic homeostasis. FEBS Letters, 589(15), 1728–1734. https://doi.org/10.1016/j.febslet.2015.05.054
Reigstad, C. S., et al. (2015). Gut microbes promote colonic serotonin production through short-chain fatty acids. The FASEB Journal, 29(4), 1395–1403. https://doi.org/10.1096/fj.14-259598
Fernstrom, J. D. (2013). Large neutral amino acids: dietary effects on brain neurochemistry and function. Amino Acids, 45(3), 419–430. https://doi.org/10.1007/s00726-012-1330-y
Correia, A. S., et al. (2022). Tryptophan metabolism in depression: serotonin and kynurenine pathways. International Journal of Molecular Sciences, 23(15), 8493. https://doi.org/10.3390/ijms23158493
Larrieu, T., et al. (2018). Food for mood: relevance of nutritional omega-3 fatty acids for depression and anxiety. Frontiers in Physiology, 9, 1047. https://doi.org/10.3389/fphys.2018.01047
↑ Zum VerzeichnisMelatonin (Schlaf-Wach-Rhythmus)
Themen: Zirbeldrüse und innere Uhr, Licht und Melatoninproduktion, antioxidative Eigenschaften, Dosierungsfragen.
Claustrat, B., et al. (2005). The basic physiology and pathophysiology of melatonin. Sleep Medicine Reviews, 9(1), 11–24. https://doi.org/10.1016/j.smrv.2004.08.001
Dumont, M., et al. (2011). Melatonin production and light exposure of rotating night workers. Chronobiology International, 29(2), 203–210. https://doi.org/10.3109/07420528.2011.647177
Reiter, R. J., et al. (2000). Actions of melatonin in the reduction of oxidative stress: a review. Journal of Biomedical Science, 7(6), 444–458. https://doi.org/10.1007/BF02253360
Zhdanova, I. V., et al. (2001). Melatonin treatment for age-related insomnia. The Journal of Clinical Endocrinology & Metabolism, 86(10), 4727–4730. https://doi.org/10.1210/jcem.86.10.7901
↑ Zum VerzeichnisWachstumshormone (Reparatur & Fettverbrennung)
Themen: Tiefschlaf und GH-Ausschüttung, Fasten und GH, Insulin und viszerales Fett als Gegenspieler, Hitze- und Belastungsreize, altersabhängiger Rückgang.
Van Cauter, E., et al. (2000). Interrelationships between growth hormone and sleep. Growth Hormone & IGF Research, 10(Suppl. B), S57–S62. https://doi.org/10.1016/S1096-6374(00)80011-8
Ho, K. Y., et al. (1988). Fasting enhances growth hormone secretion and amplifies its complex rhythms in man. Journal of Clinical Investigation, 81(4), 968–975. https://doi.org/10.1172/JCI113450
Jezova, D., et al. (2009). Growth hormone response to different consecutive stress stimuli in healthy men. Stress, 10(2), 205–211. https://doi.org/10.1080/10253890701292168
Corpas, E., et al. (1993). Human growth hormone and human aging. Endocrine Reviews, 14(1), 20–39. https://doi.org/10.1210/edrv-14-1-20
↑ Zum VerzeichnisDHEA (Stresspuffer & Hormonvorstufe)
Themen: DHEA als antiglukokortikoider Gegenspieler, DHEA-S unter chronischer Belastung, Cortisol-DHEA-Verhältnis, altersabhängiger Rückgang, Glukosestoffwechsel im Muskel.
Kalimi, M., et al. (1994). Anti-glucocorticoid effects of dehydroepiandrosterone (DHEA). Molecular and Cellular Biochemistry, 131(2), 99–104. https://doi.org/10.1007/BF00925945
Lennartsson, A. K., et al. (2022). DHEA-S production capacity in relation to perceived prolonged stress. Stress, 25(1), 105–112. https://doi.org/10.1080/10253890.2021.2024803
do Vale, S., et al. (2014). The relationship between DHEA, working memory and distraction. PLOS ONE, 9(8), e104869. https://doi.org/10.1371/journal.pone.0104869
Baulieu, E. E., et al. (2000). DHEA, DHEA sulfate, and aging: contribution of the DHEAge Study. Proceedings of the National Academy of Sciences, 97(8), 4279–4284. https://doi.org/10.1073/pnas.97.8.4279
Sato, K., et al. (2008). Testosterone and DHEA activate the glucose metabolism-related signaling pathway in skeletal muscle. American Journal of Physiology-Endocrinology and Metabolism, 294(5), E961–E968. https://doi.org/10.1152/ajpendo.00678.2007
↑ Zum VerzeichnisProgesteron (Ruhe & hormonelle Balance)
Themen: Allopregnanolon am GABA-A-Rezeptor, Lutealphase und Zyklusdynamik, Basaltemperatur, Vitex agnus-castus bei PMS.
Bäckström, T., et al. (2014). Allopregnanolone and mood disorders. Progress in Neurobiology, 113, 88–94. https://doi.org/10.1016/j.pneurobio.2013.07.005
Taraborrelli, S. (2015). Physiology, production and action of progesterone. Acta Obstetricia et Gynecologica Scandinavica, 94(Suppl. 161), 8–16. https://doi.org/10.1111/aogs.12771
Verkaik, S., et al. (2017). The treatment of premenstrual syndrome with preparations of Vitex agnus castus. American Journal of Obstetrics and Gynecology, 217(2), 150–166. https://doi.org/10.1016/j.ajog.2017.02.028
↑ Zum VerzeichnisTestosteron (Status & Durchsetzungsfähigkeit)
Themen: Testosteron, Verhalten und körperliche Merkmale; Ursachen niedriger Werte; Zink; Krafttraining; Ernährung und Testosteronspiegel.
Zitzmann, M., et al. (2001). Testosterone levels in healthy men and the relation to behavioural and physical characteristics. European Journal of Endocrinology, 144(3), 183–197. https://doi.org/10.1530/eje.0.1440183
Wrzosek, M., et al. (2020). The causes of adverse changes of testosterone levels in men. Expert Review of Endocrinology & Metabolism, 15(5), 355–362. https://doi.org/10.1080/17446651.2020.1813020
Prasad, A. S., et al. (1997). Zinc status and serum testosterone levels of healthy adults. Nutrition, 12(5), 344–348. https://doi.org/10.1016/S0899-9007(96)80058-X
Volek, J. S., et al. (1997). Testosterone and cortisol in relationship to dietary nutrients and resistance exercise. Journal of Applied Physiology, 82(1), 49–54. https://doi.org/10.1152/jappl.1997.82.1.49
Zamir, A., et al. (2021). Manipulation of dietary intake on changes in circulating testosterone concentrations. Nutrients, 13(10), 3375. https://doi.org/10.3390/nu13103375
↑ Zum VerzeichnisÖstrogene (Zyklusregulation & Neuroplastizität)
Themen: synaptische Plastizität und Neurogenese, Aromatase und Körperfett, Insulinsensitivität und Fettverteilung, endokrin wirksame Umweltstoffe.
Sheppard, P. A. S., et al. (2019). Estrogenic modulation of memory and the structural plasticity of the hippocampus. Molecular Brain, 12, 86. https://doi.org/10.1186/s13041-019-0442-7
Lizcano, F., et al. (2014). Estrogen deficiency and the origin of obesity during menopause. BioMed Research International, 2014, 757461. https://doi.org/10.1155/2014/757461
Mauvais-Jarvis, F., et al. (2013). The role of estrogens in control of energy balance and glucose homeostasis. Endocrine Reviews, 34(3), 309–338. https://doi.org/10.1210/er.2012-1055
Diamanti-Kandarakis, E., et al. (2009). Endocrine-disrupting chemicals: an Endocrine Society scientific statement. Endocrine Reviews, 30(4), 293–342. https://doi.org/10.1210/er.2009-0002
↑ Zum VerzeichnisOxytocin (Bindung & Sicherheit)
Themen: Oxytocin und Stressdämpfung bei sozialer Sicherheit, kardiovaskuläre Effekte, Kontext- und Personenabhängigkeit, Gruppendynamik.
Uvnäs-Moberg, K. (1998). Oxytocin may mediate the benefits of positive social interaction and emotions. Psychoneuroendocrinology, 23(8), 819–835. https://doi.org/10.1016/S0306-4530(98)00056-0
Bartz, J. A., et al. (2011). Social effects of oxytocin in humans: context and person matter. Trends in Cognitive Sciences, 15(7), 301–309. https://doi.org/10.1016/j.tics.2011.05.002
De Dreu, C. K. W., et al. (2011). Oxytocin promotes human ethnocentrism. Proceedings of the National Academy of Sciences, 108(4), 1262–1266. https://doi.org/10.1073/pnas.1015316108
↑ Zum VerzeichnisEndorphine (Schmerz & Belastungstoleranz)
Themen: körpereigene Opioidpeptide (POMC/β-Lipotropin), intensive Belastung und β-Endorphin, soziales Lachen und Schmerzschwelle.
Chrétien, M., et al. (1979). From β-lipotropin to β-endorphin and „pro-opio-melanocortin". Canadian Journal of Biochemistry, 57(9), 1111–1121. https://doi.org/10.1139/o79-143
Heitkamp, H. C., et al. (1993). β-endorphin and adrenocorticotropic hormone production during marathon and incremental exercise. European Journal of Applied Physiology and Occupational Physiology, 66(3), 269–274. https://doi.org/10.1007/BF00235105
Dunbar, R. I. M., et al. (2012). Social laughter is correlated with an elevated pain threshold. Proceedings of the Royal Society B, 279(1731), 1161–1167. https://doi.org/10.1098/rspb.2011.1373
↑ Zum VerzeichnisEndocannabinoide (Stress-Puffer & Ausgleichsregler)
Themen: Fettsäureherkunft und Omega-6-zu-Omega-3-Verhältnis, Bewegung und Anandamid, Immun- und Entzündungsregulation.
Banni, S., et al. (2010). Effect of dietary fat on endocannabinoids and related mediators. Molecular Nutrition & Food Research, 54(1), 82–92. https://doi.org/10.1002/mnfr.200900516
Hansen, H. S., et al. (2008). Endocannabinoids and nutrition. Journal of Neuroendocrinology, 20(Suppl. 1), 94–99. https://doi.org/10.1111/j.1365-2826.2008.01687.x
Fuss, J., et al. (2015). A runner's high depends on cannabinoid receptors in mice. Proceedings of the National Academy of Sciences, 112(42), 13105–13108. https://doi.org/10.1073/pnas.1514996112
Pandey, R., et al. (2009). Endocannabinoids and immune regulation. Pharmacological Research, 60(2), 85–92. https://doi.org/10.1016/j.phrs.2009.03.019
↑ Zum VerzeichnisDarm-Mikrobiom (Regulationsdrehkreuz)
Themen: Mikrobiom in Gesundheit und Krankheit, kurzkettige Fettsäuren und Darm-Hirn-Achse, Östrobolom und Östrogen-Recycling.
Young, V. B. (2017). The role of the microbiome in human health and disease: an introduction for clinicians. BMJ, 356, j831. https://doi.org/10.1136/bmj.j831
Pflughoeft, K. J., et al. (2012). Human microbiome in health and disease. Annual Review of Pathology: Mechanisms of Disease, 7, 99–122. https://doi.org/10.1146/annurev-pathol-011811-132421
Dalile, B., et al. (2019). The role of short-chain fatty acids in microbiota–gut–brain communication. Nature Reviews Gastroenterology & Hepatology, 16(8), 461–478. https://doi.org/10.1038/s41575-019-0157-3
Ervin, S. M., et al. (2019). Gut microbial β-glucuronidases reactivate estrogens as components of the estrobolome. Journal of Biological Chemistry, 294(49), 18586–18599. https://doi.org/10.1074/jbc.RA119.010950
↑ Zum VerzeichnisMitochondrien versorgen
Themen: mitochondriale Funktion und Bioenergetik, B-Vitamine als Kofaktoren der Energieproduktion.
San-Millán, I. (2023). The key role of mitochondrial function in health and disease. Antioxidants, 12(4), 782. https://doi.org/10.3390/antiox12040782
Mukherjee, S., et al. (2023). The role of B vitamins in protecting mitochondrial function. In Molecular Nutrition and Mitochondria (S. 167–193). Academic Press. https://doi.org/10.1016/B978-0-323-90256-4.00019-5
↑ Zum VerzeichnisMitochondrien-Neubildung
Themen: Ausdauertraining und mitochondriale Biogenese (PGC-1α), Trainingsdosis, Krafttraining im Vergleich.
Abrego-Guandique, D. M., et al. (2025). The impact of exercise on mitochondrial biogenesis in skeletal muscle: a systematic review and meta-analysis. Biomolecular Concepts, 16(1), 20250055. https://doi.org/10.1515/bmc-2025-0055
Bishop, D. J., et al. (2014). Can we optimise the exercise training prescription to maximise improvements in mitochondria function and content? Biochimica et Biophysica Acta – General Subjects, 1840(4), 1266–1275. https://doi.org/10.1016/j.bbagen.2013.10.012
Groennebaek, T., et al. (2017). Impact of resistance training on skeletal muscle mitochondrial biogenesis, content, and function. Frontiers in Physiology, 8, 713. https://doi.org/10.3389/fphys.2017.00713
↑ Zum VerzeichnisMitochondrien pflegen
Themen: reaktive Sauerstoffspezies und Alterung, Tiefschlaf und mitochondriale Reparatur, B-Vitamine, Advanced Glycation End-Products.
Brand, M. D., et al. (2013). The role of mitochondrial function and cellular bioenergetics in ageing and disease. British Journal of Dermatology, 169(Suppl. 2), 1–8. https://doi.org/10.1111/bjd.12208
Sarnataro, R. (2025). Neurobiology of mitochondrial dynamics in sleep. The Journal of Physiology. https://doi.org/10.1113/JP288054
Mukherjee, S., et al. (2023). The role of B vitamins in protecting mitochondrial function. In Molecular Nutrition and Mitochondria (S. 167–193). Academic Press. https://doi.org/10.1016/B978-0-323-90256-4.00019-5
Patel, S. H., et al. (2019). Advanced glycation end-products suppress mitochondrial function and proliferative capacity. Scientific Reports, 9(1), 12614. https://doi.org/10.1038/s41598-019-49062-8
↑ Zum VerzeichnisMitochondrien pflegen – Smoothie
Themen: Polyphenole und Mitochondrienfunktion, funktionelle Lebensmittel und gesundes Altern, mitochondriale DNA-Kopienzahl, Kakao-Inhaltsstoffe.
Gibellini, L., et al. (2015). Natural compounds modulating mitochondrial functions. Evidence-Based Complementary and Alternative Medicine, 2015, 527209. https://doi.org/10.1155/2015/527209
Navarro-Hortal, M. D., et al. (2023). Molecular bases for the use of functional foods in the management of healthy aging. Critical Reviews in Food Science and Nutrition, 63(33), 11967–11986. https://doi.org/10.1080/10408398.2022.2098244
Kim, M. B., et al. (2024). Targeting mitochondrial dysfunction by bioactive food components. Journal of Lipid and Atherosclerosis, 13(3), 306–327. https://doi.org/10.12997/jla.2024.13.3.306
Perri, M. R., et al. (2026). Modulation of mitochondrial DNA copy number: therapeutic potential of phytochemicals and plant extracts. Archives of Pharmacal Research. https://doi.org/10.1007/s12272-026-01620-1
Chidambaram, S. B., et al. (2018). Cocoa beans improve mitochondrial biogenesis via PPARγ/PGC1α dependent signalling. Nutritional Neuroscience, 23(6), 471–480. https://doi.org/10.1080/1028415X.2018.1521088
↑ Zum VerzeichnisAußenreize zur Mitochondrienaktivierung
Themen: passive Hitze (Sauna) und Hitzeschockproteine, Kälte und braunes Fettgewebe, Photobiomodulation (Rot- und Nahinfrarotlicht).
Laukkanen, J. A., et al. (2024). The multifaceted benefits of passive heat therapies for extending the healthspan. Temperature, 11(1), 27–51. https://doi.org/10.1080/23328940.2023.2300623
Blondin, D. P., et al. (2014). Increased brown adipose tissue oxidative capacity in cold-acclimated humans. The Journal of Clinical Endocrinology & Metabolism, 99(3), E438–E446. https://doi.org/10.1210/jc.2013-3901
Hamblin, M. R. (2018). Mechanisms and mitochondrial redox signaling in photobiomodulation. Photochemistry and Photobiology, 94(2), 199–212. https://doi.org/10.1111/php.12864
↑ Zum VerzeichnisSupplements für Mitochondrien – Basis
Themen: Magnesium im Energiestoffwechsel, Vitamin D und mitochondriale Funktion, B-Vitamine.
Liu, M., et al. (2025). Magnesium homeostasis and magnesium transporters in human health. Nutrients, 17(5), 920. https://doi.org/10.3390/nu17050920
Sinha, A., et al. (2013). Improving the vitamin D status of vitamin D deficient adults is associated with improved mitochondrial oxidative function in skeletal muscle. The Journal of Clinical Endocrinology & Metabolism, 98(3), E509–E513. https://doi.org/10.1210/jc.2012-3592
Depeint, F., et al. (2006). Mitochondrial function and toxicity: role of the B vitamin family on mitochondrial energy metabolism. Chemico-Biological Interactions, 163(1–2), 94–112. https://doi.org/10.1016/j.cbi.2006.04.014
↑ Zum VerzeichnisSupplements für Mitochondrien – Fortgeschritten
Themen: Kreatin für Kraft und Kognition, Coenzym Q10 in der Atmungskette, PQQ und Biogenese, Acetyl-L-Carnitin, N-Acetylcystein, Lutein und Zeaxanthin, Alpha-Liponsäure.
Kazeminasab, F., et al. (2025). The effects of creatine supplementation on upper- and lower-body strength and power. Nutrients, 17(17), 2748. https://doi.org/10.3390/nu17172748
Xu, C., et al. (2024). The effects of creatine supplementation on cognitive function in adults. Frontiers in Nutrition, 11, 1424972. https://doi.org/10.3389/fnut.2024.1424972
Hernández-Camacho, J. D., et al. (2018). Coenzyme Q10 supplementation in aging and disease. Frontiers in Physiology, 9, 44. https://doi.org/10.3389/fphys.2018.00044
Chowanadisai, W., et al. (2010). Pyrroloquinoline quinone stimulates mitochondrial biogenesis through CREB phosphorylation and increased PGC-1α expression. Journal of Biological Chemistry, 285(1), 142–152. https://doi.org/10.1074/jbc.M109.030130
Jones, L. L., et al. (2010). Acylcarnitines: role in brain. Progress in Lipid Research, 49(1), 61–75. https://doi.org/10.1016/j.plipres.2009.08.004
Medved, I., et al. (2004). N-acetylcysteine enhances muscle cysteine and glutathione availability and attenuates fatigue during prolonged exercise. Journal of Applied Physiology, 97(4), 1477–1485. https://doi.org/10.1152/japplphysiol.00371.2004
Merry, T. L., et al. (2016). Do antioxidant supplements interfere with skeletal muscle adaptation to exercise training? The Journal of Physiology, 594(18), 5135–5147. https://doi.org/10.1113/JP270654
Bernstein, P. S., et al. (2016). Lutein, zeaxanthin, and meso-zeaxanthin: the basic and clinical science underlying carotenoid-based nutritional interventions against ocular disease. Progress in Retinal and Eye Research, 50, 34–66. https://doi.org/10.1016/j.preteyeres.2015.10.003
Age-Related Eye Disease Study 2 (AREDS2) Research Group. (2013). Lutein + zeaxanthin and omega-3 fatty acids for age-related macular degeneration. JAMA, 309(19), 2005–2015. https://doi.org/10.1001/jama.2013.4997
Shay, K. P., et al. (2009). Alpha-lipoic acid as a dietary supplement: molecular mechanisms and therapeutic potential. Biochimica et Biophysica Acta – General Subjects, 1790(10), 1149–1160. https://doi.org/10.1016/j.bbagen.2009.07.026
↑ Zum VerzeichnisSystemische Steuerung der Zellenergie
Themen: Stress und mitochondriale Effizienz, Schilddrüse und Energieumsatz. Zu Mitophagie und Urolithin A siehe „Stoffwechsel verbessern".
Picard, M., et al. (2018). Psychological stress and mitochondria: a systematic review. Psychosomatic Medicine, 80(2), 141–153. https://doi.org/10.1097/PSY.0000000000000545
Cioffi, F., et al. (2022). Bioenergetic aspects of mitochondrial actions of thyroid hormones. Cells, 11(6), 997. https://doi.org/10.3390/cells11060997
↑ Zum VerzeichnisStoffwechsel verbessern
Themen: Fasten und metabolischer Switch (mTOR, Autophagie, AMPK), Sirtuine und NAD⁺, Urolithin A und Mitophagie.
de Cabo, R., et al. (2019). Effects of intermittent fasting on health, aging, and disease. New England Journal of Medicine, 381(26), 2541–2551. https://doi.org/10.1056/NEJMra1905136
Kincaid, B., et al. (2013). Forever young: SIRT3 – a shield against mitochondrial meltdown, aging, and neurodegeneration. Frontiers in Aging Neuroscience, 5, 48. https://doi.org/10.3389/fnagi.2013.00048
Ryu, D., et al. (2016). Urolithin A induces mitophagy and prolongs lifespan in C. elegans and increases muscle function in rodents. Nature Medicine, 22(8), 879–888. https://doi.org/10.1038/nm.4132
Andreux, P. A., et al. (2019). The mitophagy activator urolithin A is safe and induces a molecular signature of improved mitochondrial and cellular health in humans. Nature Metabolism, 1(6), 595–603. https://doi.org/10.1038/s42255-019-0073-4
↑ Zum VerzeichnisMolekulare Schalter
Themen: mTOR und AMPK als Wachstums- und Energiesensoren, NRF2 und antioxidative Enzyme (Sulforaphan), Sirtuine und DNA-Reparatur.
de Cabo, R., et al. (2019). Effects of intermittent fasting on health, aging, and disease. New England Journal of Medicine, 381(26), 2541–2551. https://doi.org/10.1056/NEJMra1905136
Holmström, K. M., et al. (2016). The multifaceted role of Nrf2 in mitochondrial function. Current Opinion in Toxicology, 1, 80–91. https://doi.org/10.1016/j.cotox.2016.10.002
Kincaid, B., et al. (2013). Forever young: SIRT3 – a shield against mitochondrial meltdown, aging, and neurodegeneration. Frontiers in Aging Neuroscience, 5, 48. https://doi.org/10.3389/fnagi.2013.00048
↑ Zum VerzeichnisVerbreitete ungünstige Genvarianten I
Themen: MTHFR C677T und Folatstoffwechsel, PEMT und Cholinbedarf, APOE4 und Fettstoffwechsel, CYP1A2 und Koffeinabbau, Glutathion-Peroxidasen und Selen.
Liew, S.-C., et al. (2015). Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism: epidemiology, metabolism and associated diseases. European Journal of Medical Genetics, 58(1), 1–10. https://doi.org/10.1016/j.ejmg.2014.10.004
Tan, X., et al. (2016). PEMT gene rs7946 polymorphism plays a role in risk of non-alcoholic fatty liver disease. Pharmacogenetics and Genomics, 26(2), 88–95. https://doi.org/10.1097/FPC.0000000000000193
Carvalho-Wells, A. L., et al. (2012). APOE genotype influences triglyceride and C-reactive protein responses to altered dietary fat intake. The American Journal of Clinical Nutrition, 96(6), 1447–1453. https://doi.org/10.3945/ajcn.112.043240
Cornelis, M. C., et al. (2006). Coffee, CYP1A2 genotype, and risk of myocardial infarction. JAMA, 295(10), 1135–1141. https://doi.org/10.1001/jama.295.10.1135
Lubos, E., et al. (2011). Glutathione peroxidase-1 in health and disease: from molecular mechanisms to therapeutic opportunities. Antioxidants & Redox Signaling, 15(7), 1957–1997. https://doi.org/10.1089/ars.2010.3586
↑ Zum VerzeichnisVerbreitete ungünstige Genvarianten II
Themen: NOS3 und Stickstoffmonoxid, DAO/AOC1 und Histaminabbau, COMT Val158Met und Catecholamine, MAOA und Monoamine, SOD2 und mitochondriale Radikalabwehr.
Oliveira-Paula, G. H., et al. (2016). Endothelial nitric oxide synthase: from biochemistry and gene structure to clinical implications of NOS3 polymorphisms. Gene, 575(2, Pt 3), 584–599. https://doi.org/10.1016/j.gene.2015.09.061
Comas-Basté, O., et al. (2020). Histamine intolerance: the current state of the art. Biomolecules, 10(8), 1181. https://doi.org/10.3390/biom10081181
Hernaus, D., et al. (2013). COMT Val158Met genotype selectively alters prefrontal [18F]fallypride displacement and subjective feelings of stress. PLOS ONE, 8(6), e65662. https://doi.org/10.1371/journal.pone.0065662
Kolla, N. J., et al. (2020). The role of monoamine oxidase A in the neurobiology of aggressive, antisocial, and violent behavior. Progress in Neurobiology, 194, 101875. https://doi.org/10.1016/j.pneurobio.2020.101875
Flynn, J. M., et al. (2013). SOD2 in mitochondrial dysfunction and neurodegeneration. Free Radical Biology and Medicine, 62, 4–12. https://doi.org/10.1016/j.freeradbiomed.2013.05.027
↑ Zum VerzeichnisMonitoring & Biofeedback (Schlaf)
Themen: Genauigkeit kommerzieller Wearables beim Schlaftracking.
Robbins, R., et al. (2024). Accuracy of three commercial wearable devices for sleep tracking in healthy adults. Sensors, 24(20), 6532. https://doi.org/10.3390/s24206532
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