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Pollen Alters Amino Acid Levels in the Honey Bee Brain and This Relationship Changes With Age and Parasitic Stress

https://doi.org/10.3389/fnins.2020.00231

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Limits on volume changes in the mushroom bodies of the honey bee brain

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Foraging experience, glomerulus volume, and synapse number: A stereological study of the honey bee antennal lobe

inferredcites →https://doi.org/10.1006/hbeh.2002.1806openalex-snapshot

Juvenile Hormone and Octopamine in the Regulation of Division of Labor in Honey Bee Colonies

inferredcites →https://doi.org/10.1007/978-3-642-02624-9_4openalex-snapshot

Honeybee cognition

inferredcites →https://doi.org/10.1007/s00265-002-0457-3openalex-snapshot

How honeybees ( Apis mellifera L.) change their broodcare behaviour in response to non-foraging conditions and poor pollen conditions

inferredcites →https://doi.org/10.1007/s002650050442openalex-snapshot

Effects of colony food shortage on behavioral development in honey bees

inferredcites →https://doi.org/10.1007/s003590050347openalex-snapshot

Biogenic amines and division of labor in honey bee colonies

inferredcites →https://doi.org/10.1007/s003590050348openalex-snapshot

Biogenic amines and division of labor in honey bee colonies: behaviorally related changes in the antennal lobes and age-related changes in the mushroom bodies

inferredcites →https://doi.org/10.1007/s003590100226openalex-snapshot

Cannibalism and early capping: strategy of honeybee colonies in times of experimental pollen shortages

inferredcites →https://doi.org/10.1007/s00726-009-0269-0openalex-snapshot

Amino acids: metabolism, functions, and nutrition

inferredcites →https://doi.org/10.1007/s13592-018-0617-8openalex-snapshot

Transcriptional and physiological responses of hypopharyngeal glands in honeybees (Apis mellifera L.) infected by Nosema ceranae

inferredcites →https://doi.org/10.1016/0022-1910(89)90121-2openalex-snapshot

Influence of diet, age and colony condition upon intestinal proteolytic activity and size of the hypopharyngeal glands in the honeybee (Apis mellifera L.)

inferredcites →https://doi.org/10.1016/0022-2011(69)90098-6openalex-snapshot

Histological comparisons of the development of hypopharyngeal glands in healthy and Nosema-infected worker honey bees

inferredcites →https://doi.org/10.1016/0022-2011(71)90002-4openalex-snapshot

Ultrastructural changes in the hypopharyngeal glands of worker honey bees infected by Nosema apis

inferredcites →https://doi.org/10.1016/0304-3940(95)11913-hopenalex-snapshot

Neurogenesis is absent in the brains of adult honey bees and does not explain behavioral neuroplasticity

inferredcites →https://doi.org/10.1016/j.anbehav.2004.03.017openalex-snapshot

Worker nutrition and division of labour in honeybees

inferredcites →https://doi.org/10.1016/j.chom.2018.05.018openalex-snapshot

Parasite Sensing of Host Nutrients and Environmental Cues

inferredcites →https://doi.org/10.1016/j.gdata.2016.09.010openalex-snapshot

Brain transcriptomes of honey bees ( Apis mellifera ) experimentally infected by two pathogens: Black queen cell virus and Nosema ceranae

inferredcites →https://doi.org/10.1016/j.ibmb.2016.10.005openalex-snapshot

Differential proteomics reveals novel insights into Nosema–honey bee interactions

inferredcites →https://doi.org/10.1016/j.jinsphys.2010.03.017openalex-snapshot

The effect of diet on protein concentration, hypopharyngeal gland development and virus load in worker honey bees (Apis mellifera L.)

inferredcites →https://doi.org/10.1016/j.jinsphys.2013.12.005openalex-snapshot

The role of serotonin in feeding and gut contractions in the honeybee

inferredcites →https://doi.org/10.1016/j.jinsphys.2015.11.016openalex-snapshot

Transcriptional, translational, and physiological signatures of undernourished honey bees (Apis mellifera) suggest a role for hormonal factors in hypopharyngeal gland degradation

inferredcites →https://doi.org/10.1016/j.jinsphys.2016.01.004openalex-snapshot

Effects of pollen dilution on infection of Nosema ceranae in honey bees

inferredcites →https://doi.org/10.1016/j.jinsphys.2018.07.002openalex-snapshot

Connecting the nutrient composition of seasonal pollens with changing nutritional needs of honey bee (Apis mellifera L.) colonies

inferredcites →https://doi.org/10.1016/j.jip.2006.11.001openalex-snapshot

Experimental infection of Apis mellifera honeybees with Nosema ceranae (Microsporidia)

inferredcites →https://doi.org/10.1016/j.jip.2008.12.001openalex-snapshot

Energetic stress in the honeybee Apis mellifera from Nosema ceranae infection

inferredcites →https://doi.org/10.1016/j.jip.2010.12.005openalex-snapshot

Pathological effects of the microsporidium Nosema ceranae on honey bee queen physiology (Apis mellifera)

inferredcites →https://doi.org/10.1016/j.jip.2014.07.002openalex-snapshot

Differential proteomic analysis of midguts from Nosema ceranae-infected honeybees reveals manipulation of key host functions

inferredcites →https://doi.org/10.1016/j.lmot.2014.10.007openalex-snapshot

The effects of acute stress on learning and memory in bumblebees

inferredcites →https://doi.org/10.1016/j.neubiorev.2011.07.002openalex-snapshot

Stress effects on memory: An update and integration

inferredcites →https://doi.org/10.1016/s0021-9673(98)00721-3openalex-snapshot

Hydrolysis and amino acid composition analysis of proteins

inferredcites →https://doi.org/10.1016/s0149-7634(02)00012-xopenalex-snapshot

Effects of prenatal protein malnutrition on the hippocampal formation

inferredcites →https://doi.org/10.1016/s0896-6273(00)80073-2openalex-snapshot

Inhibition of Nitric Oxide Synthase Impairs a Distinct Form of Long-Term Memory in the Honeybee, Apis mellifera

inferredcites →https://doi.org/10.1038/364238a0openalex-snapshot

Selective neuroanatomical plasticity and division of labour in the honeybee

inferredcites →https://doi.org/10.1038/nature23009openalex-snapshot

Nutrient sensing modulates malaria parasite virulence

inferredcites →https://doi.org/10.1051/apido:2000130openalex-snapshot

Pollen quality of fresh and 1-year-old single pollen diets for worker honey bees (Apis melliferaL.)

inferredcites →https://doi.org/10.1073/pnas.0800630105openalex-snapshot

Insulin signaling is involved in the regulation of worker division of labor in honey bee colonies

inferredcites →https://doi.org/10.1073/pnas.1517375112openalex-snapshot

Omega-3 deficiency impairs honey bee learning

inferredcites →https://doi.org/10.1080/0005772x.2003.11099566openalex-snapshot

The amazing mini-brain: lessons from a honey bee

inferredcites →https://doi.org/10.1080/00218839.1967.11100176openalex-snapshot

The Rate of Pollen Consumption by Newly Emerged Honeybees

inferredcites →https://doi.org/10.1093/jisesa/iev142openalex-snapshot

The Appropriate Supplementary Level of Tryptophan in the Diet of Apis mellifera (Hymenoptera: Apidae) Worker Bees

inferredcites →https://doi.org/10.1097/00001756-199702100-00042openalex-snapshot

The effects of age on olfactory learning and memory in the honey bee Apis mellifera

inferredcites →https://doi.org/10.1101/lm.40001openalex-snapshot

Massed and Spaced Learning in Honeybees: The Role of CS, US, the Intertrial Interval, and the Test Interval

inferredcites →https://doi.org/10.1111/imb.12190openalex-snapshot

Nosema ceranae alters a highly conserved hormonal stress pathway in honeybees

inferredcites →https://doi.org/10.1146/annurev.en.15.010170.001043openalex-snapshot

Honey Bee Nutrition

inferredcites →https://doi.org/10.1146/annurev.ento.010908.164537openalex-snapshot

Honey Bees as a Model for Vision, Perception, and Cognition

inferredcites →https://doi.org/10.1159/000067788openalex-snapshot

A Role for Octopamine in Honey Bee Division of Labor

inferredcites →https://doi.org/10.1159/000111474openalex-snapshot

Juvenile Hormone, Behavioral Maturation, and Brain Structure in the Honey Bee

inferredcites →https://doi.org/10.1186/1471-2164-14-451openalex-snapshot

Genome sequencing and comparative genomics of honey bee microsporidia, Nosema apis reveal novel insights into host-parasite interactions

inferredcites →https://doi.org/10.1186/1471-2164-14-799openalex-snapshot

Chronic parasitization by Nosema microsporidia causes global expression changes in core nutritional, metabolic and behavioral pathways in honey bee workers (Apis mellifera)

inferredcites →https://doi.org/10.1186/1471-2164-15-134openalex-snapshot

Transcriptional markers of sub-optimal nutrition in developing Apis mellifera nurse workers

inferredcites →https://doi.org/10.1186/1472-6785-13-25openalex-snapshot

Ecto- and endoparasite induce similar chemical and brain neurogenomic responses in the honey bee (Apis mellifera)

inferredcites →https://doi.org/10.1242/jeb.086694openalex-snapshot

Nitric oxide affects short-term olfactory memory in the antennal lobe ofManduca Sexta

inferredcites →https://doi.org/10.1242/jeb.161489openalex-snapshot

Nosema ceranae parasitism impacts olfactory learning and memory and neurochemistry in honey bees (Apis mellifera)

inferredcites →https://doi.org/10.1242/jeb.173336openalex-snapshot

Eating when ill is risky: immune defense impairs food detoxification in the caterpillar,Manduca sexta

inferredcites →https://doi.org/10.1371/journal.pone.0025371openalex-snapshot

Dopamine and Octopamine Influence Avoidance Learning of Honey Bees in a Place Preference Assay

inferredcites →https://doi.org/10.1371/journal.pone.0058165openalex-snapshot

Physiological and Behavioral Changes in Honey Bees (Apis mellifera) Induced by Nosema ceranae Infection

inferredcites →https://doi.org/10.1371/journal.pone.0072016openalex-snapshot

Influence of Pollen Nutrition on Honey Bee Health: Do Pollen Quality and Diversity Matter?

inferredcites →https://doi.org/10.1371/journal.pone.0132014openalex-snapshot

Characterizing the Impact of Commercial Pollen Substitute Diets on the Level of Nosema spp. in Honey Bees (Apis mellifera L.)

inferredcites →https://doi.org/10.1371/journal.pone.0187726openalex-snapshot

Dietary amino acid and vitamin complex protects honey bee from immunosuppression caused by Nosema ceranae

inferredcites →https://doi.org/10.1523/jneurosci.21-16-06395.2001openalex-snapshot

Experience- and Age-Related Outgrowth of Intrinsic Neurons in the Mushroom Bodies of the Adult Worker Honeybee

inferredcites →https://doi.org/10.1603/ec13520openalex-snapshot

Spore Loads May Not be Used Alone as a Direct Indicator of the Severity of Nosema ceranae Infection in Honey Bees Apis mellifera (Hymenoptera:Apidae)

inferredcites →https://doi.org/10.3389/fnhum.2013.00097openalex-snapshot

The role of nutrition in children's neurocognitive development, from pregnancy through childhood

inferredcites →https://doi.org/10.3389/fnsys.2014.00059openalex-snapshot

The role of nitric oxide in memory is modulated by diurnal time

inferredcites →https://doi.org/10.3896/ibra.1.52.1.14openalex-snapshot

Standard methods forNosemaresearch

inferredcites →https://doi.org/10.3896/ibra.1.52.4.10openalex-snapshot

Miscellaneous standard methods forApis melliferaresearch

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4482323openalex-extracted

Studies on the Effect of Nonthermally-Treated Pollen on Colony Reproductive Output in Commercial Bumblebees (Bombus Terrestris)

inferred← citeshttps://doi.org/10.1007/s00216-024-05368-9openalex-snapshot

Application of a robust MALDI mass spectrometry approach for bee pollen investigation

inferred← citeshttps://doi.org/10.1007/s00265-023-03299-6openalex-snapshot

Bumblebee cognitive abilities are robust to changes in colony size

inferred← citeshttps://doi.org/10.1016/j.aspen.2022.101967openalex-snapshot

Comparison of physicochemical properties of pollen substitute diet for honey bee (Apis mellifera)

inferred← citeshttps://doi.org/10.1016/j.envadv.2026.100709openalex-snapshot

Interactions between the gut parasite Nosema ceranae and multiple stressors in the honeybee Apis mellifera

inferred← citeshttps://doi.org/10.1016/j.jinsphys.2021.104270openalex-snapshot

Regulation of dopamine production in the brains during sexual maturation in male honey bees

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.165614openalex-snapshot

Studies on the novel effects of electron beam treated pollen on colony reproductive output in commercially-reared bumblebees (Bombus terrestris) for mass pollination applications

inferred← citeshttps://doi.org/10.1038/s41559-022-01840-wopenalex-snapshot

The gut microbiota affects the social network of honeybees

inferred← citeshttps://doi.org/10.1038/s41598-025-96649-5openalex-snapshot

Unravelling pollen diet and microbiome influence on honey bee health

inferred← citeshttps://doi.org/10.1039/d2mo00046fopenalex-snapshot

Metabolomic analysis of honey bee ( Apis mellifera L.) response to glyphosate exposure

inferred← citeshttps://doi.org/10.1093/jee/toae176openalex-snapshot

Effect of artificial sugar supplement on the lifespan and learning memory ability of honey bee (Apis cerana) worker bee offspring

inferred← citeshttps://doi.org/10.1098/rspb.2024.3078openalex-snapshot

A nutritionally complete pollen-replacing diet protects honeybee colonies during stressful commercial pollination—requirement for isofucosterol

inferred← citeshttps://doi.org/10.1101/2024.09.22.614346openalex-snapshot

Peasants at the queen’s table?: The microbiome’s dynamics throughout swarming preparation in honey bees ( Apis mellifera )

inferred← citeshttps://doi.org/10.1111/1365-2435.14143openalex-snapshot

Macronutrient balance has opposing effects on cognition and survival in honey bees

inferred← citeshttps://doi.org/10.1111/ejn.15265openalex-snapshot

Peripheral taste detection in honey bees: What do taste receptors respond to?

inferred← citeshttps://doi.org/10.1128/mbio.01131-22openalex-snapshot

Community Dynamics in Structure and Function of Honey Bee Gut Bacteria in Response to Winter Dietary Shift

inferred← citeshttps://doi.org/10.1242/jeb.250057openalex-snapshot

The impact of landscape complexity and composition on honey bee visual learning

inferred← citeshttps://doi.org/10.1242/jeb.251673openalex-snapshot

Age-related differences in learning, memory and brain plasticity in workers of the common wasp, Vespula vulgaris

inferred← citeshttps://doi.org/10.2478/aoas-2025-0119openalex-snapshot

The microbiome's dynamics throughout swarming preparation in honey bees ( Apis mellifera )

inferred← citeshttps://doi.org/10.26717/bjstr.2023.51.008044openalex-snapshot

Changes in Amino Acid Pool in Rats with Brain Ischemia

inferred← citeshttps://doi.org/10.3389/fsufs.2024.1411410openalex-snapshot

Dietary foundations for pollinators: nutritional profiling of plants for bee health

inferred← citeshttps://doi.org/10.3390/insects13110985openalex-snapshot

Changes in Vitellogenin (Vg) and Stress Protein (HSP 70) in Honey Bee (Apis mellifera anatoliaca) Groups under Different Diets Linked with Physico-Chemical, Antioxidant and Fatty and Amino Acid Profiles

inferred← citeshttps://doi.org/10.3390/insects14010037openalex-snapshot

Hemolymph Metabolism Analysis of Honey Bee (Apis mellifera L.) Response to Different Bee Pollens

inferred← citeshttps://doi.org/10.3390/insects17060632openalex-snapshot

Metabolic and Gut Microbiome Responses to Paraquat Exposure in Apis mellifera Under Laboratory Conditions

inferred← citeshttps://doi.org/10.3390/molecules29112605openalex-snapshot

The Key Role of Amino Acids in Pollen Quality and Honey Bee Physiology—A Review

inferred← citeshttps://doi.org/10.5424/sjar/2026242-21783openalex-snapshot

Stored pollen in honeybee (Apis mellifera) colonies reveals foraging preferences and nutritional gaps in rapeseed and apple agroecosystems of southeast Spain

inferred← citeshttps://doi.org/10.58489/2836-8991/005openalex-snapshot

Distribution of the Pool of Amino Acids in The Parietal Lobe of Albino Rats

inferred← citeshttps://doi.org/10.64898/2026.05.11.724417openalex-snapshot

Layered social competition coordinates reproductive hierarchy formation in ants

inferred← citeshttps://doi.org/10.70675/6232fc0cz23a4z4e97z8184z18065d15a6efopenalex-snapshot

Effects of the neuropeptide sNPF on honey bee behaviours (Apis mellifera)

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