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Sulfakinins influence lipid composition and insulin-like peptides level in oenocytes of Zophobas atratus beetles

https://doi.org/10.1007/s00360-021-01398-2

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What this work says

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

inferredcites →https://doi.org/10.1002/arch.21350openalex-snapshot

NONSULFATED SULFAKININ CHANGES METABOLIC PARAMETERS OF INSECT FAT BODY MITOCHONDRIA

inferredcites →https://doi.org/10.1006/bbrc.2002.6459openalex-snapshot

Cloning and Functional Expression of the First Drosophila melanogaster Sulfakinin Receptor DSK-R1

inferredcites →https://doi.org/10.1007/978-1-4684-8062-7openalex-snapshot

Chromatography and Isolation of Insect Hormones and Pheromones

inferredcites →https://doi.org/10.1007/bf00305385openalex-snapshot

Localisation of sulfakinin neuronal pathways in the blowfly Calliphora vomitoria

inferredcites →https://doi.org/10.1007/s00018-015-2063-3openalex-snapshot

Insulin/IGF signaling in Drosophila and other insects: factors that regulate production, release and post-release action of the insulin-like peptides

inferredcites →https://doi.org/10.1007/s00114-003-0402-yopenalex-snapshot

Hydrocarbon synthesis by enzymatically dissociated oenocytes of the abdominal integument of the German Cockroach, Blattella germanica

inferredcites →https://doi.org/10.1007/s00360-011-0563-5openalex-snapshot

New physiological activities of myosuppressin, sulfakinin and NVP-like peptide in Zophobas atratus beetle

inferredcites →https://doi.org/10.1007/s00360-020-01300-6openalex-snapshot

Identification of sulfakinin receptors (SKR) in Tenebrio molitor beetle and the influence of sulfakinins on carbohydrates metabolism

inferredcites →https://doi.org/10.1016/0006-291x(86)91098-3openalex-snapshot

Leucosulfakinin-II, a blocked sulfated insect neuropeptide with homology to cholecystokinin and gastrin

inferredcites →https://doi.org/10.1016/0022-1910(94)00091-topenalex-snapshot

Postembryonic development of Zophobas atratus Fab. (Coleoptera: Tenebrionidae) under crowded or isolated conditions and effects of juvenile hormone analogue applications

inferredcites →https://doi.org/10.1016/0040-8166(88)90033-xopenalex-snapshot

The source of lipids and polyphenols for the insect cuticle: The role of fat body, oenocytes and oenocytoids

inferredcites →https://doi.org/10.1016/0143-4179(89)90038-3openalex-snapshot

Isolation and structure of two gastrin/CCK-like neuropeptides from the American cockroach homologous to the leucosulfakinins

inferredcites →https://doi.org/10.1016/0305-0491(88)90305-7openalex-snapshot

Lipids of the insect cuticle: origin, composition and function

inferredcites →https://doi.org/10.1016/0742-8413(92)90107-iopenalex-snapshot

Isolation, primary structure and synthesis of neomyosuppressin, a myoinhibiting neuropeptide from the grey fleshfly, Neobellieria bullata

inferredcites →https://doi.org/10.1016/j.actatropica.2016.02.021openalex-snapshot

Deltamethrin-mediated survival, behavior, and oenocyte morphology of insecticide-susceptible and resistant yellow fever mosquitos (Aedes aegypti)

inferredcites →https://doi.org/10.1016/j.ibmb.2015.03.008openalex-snapshot

Sulfakinin is an important regulator of digestive processes in the migratory locust, Locusta migratoria

inferredcites →https://doi.org/10.1016/j.jinsphys.2006.10.013openalex-snapshot

Insect satiety: Sulfakinin localization and the effect of drosulfakinin on protein and carbohydrate ingestion in the blow fly, Phormia regina (Diptera: Calliphoridae)

inferredcites →https://doi.org/10.1016/j.jinsphys.2007.04.003openalex-snapshot

RNA interference suggests sulfakinins as satiety effectors in the cricket Gryllus bimaculatus

inferredcites →https://doi.org/10.1016/j.peptides.2004.07.018openalex-snapshot

Aliphatic amino diacid Asu functions as an effective mimic of Tyr(SO3H) in sulfakinins for myotropic and food intake-inhibition activity in insects

inferredcites →https://doi.org/10.1016/j.peptides.2007.01.009openalex-snapshot

The first nonsulfated sulfakinin activity reported suggests nsDSK acts in gut biology

inferredcites →https://doi.org/10.1016/j.peptides.2007.09.020openalex-snapshot

Neuropeptides of the beetle, Tenebrio molitor identified using MALDI-TOF mass spectrometry and deduced sequences from the Tribolium castaneum genome

inferredcites →https://doi.org/10.1016/j.peptides.2013.06.009openalex-snapshot

Conserved residues in RF-NH2 receptor models identify predicted contact sites in ligand–receptor binding

inferredcites →https://doi.org/10.1016/j.peptides.2013.12.011openalex-snapshot

Characterization of sulfakinin receptor 2 and its role in food intake in the red flour beetle, Tribolium castaneum

inferredcites →https://doi.org/10.1016/j.peptides.2014.05.010openalex-snapshot

New metabolic activity of the nonsulfated sulfakinin Zopat-SK-1 in the insect fat body

inferredcites →https://doi.org/10.1016/j.peptides.2015.04.023openalex-snapshot

The activity of the nonsulfated sulfakinin Zopat-SK-1 in the neck-ligated larvae of the beetle Zophobas atratus

inferredcites →https://doi.org/10.1016/j.pneurobio.2006.07.005openalex-snapshot

A review of neurohormone GPCRs present in the fruitfly Drosophila melanogaster and the honey bee Apis mellifera

inferredcites →https://doi.org/10.1016/j.ydbio.2006.10.015openalex-snapshot

Semaphorin 2a secreted by oenocytes signals through plexin B and plexin A to guide sensory axons in the Drosophila embryo

inferredcites →https://doi.org/10.1016/j.yfrne.2007.10.003openalex-snapshot

A genome-wide inventory of neurohormone GPCRs in the red flour beetle Tribolium castaneum

inferredcites →https://doi.org/10.1016/j.ygcen.2013.03.006openalex-snapshot

Characterization of sulfakinin and sulfakinin receptor and their roles in food intake in the red flour beetle Tribolium castaneum

inferredcites →https://doi.org/10.1016/s0022-1910(00)00046-9openalex-snapshot

Sulfakinins reduce food intake in the desert locust, Schistocerca gregaria

inferredcites →https://doi.org/10.1016/s0040-8166(69)80009-1openalex-snapshot

The ultrastructure of the oenocytes in the moltiintermolt cycle of an insect

inferredcites →https://doi.org/10.1016/s0196-9781(02)00152-3openalex-snapshot

In vitro release of digestive enzymes by FMRF amide related neuropeptides and analogues in the lepidopteran insect Opisina arenosella (Walk.)

inferredcites →https://doi.org/10.1038/nature05382openalex-snapshot

Specialized hepatocyte-like cells regulate Drosophila lipid metabolism

inferredcites →https://doi.org/10.1038/s41598-019-49790-xopenalex-snapshot

Identification, Functional Characterization, and Pharmacological Analysis of Two Sulfakinin Receptors in the Medically-Important Insect Rhodnius prolixus

inferredcites →https://doi.org/10.1046/j.0014-2956.2001.02527.xopenalex-snapshot

Screening of antifeedant activity in brain extracts led to the identification of sulfakinin as a satiety promoter in the German cockroach.

inferredcites →https://doi.org/10.1073/pnas.1608295113openalex-snapshot

Cytochrome P450 associated with insecticide resistance catalyzes cuticular hydrocarbon production in Anopheles gambiae

inferredcites →https://doi.org/10.1083/jcb.56.3.870openalex-snapshot

PHENOBARBITAL-INDUCED, MEMBRANE-LIKE SCROLLS IN THE OENOCYTES OF MUSCA DOMESTICA LINNAEUS

inferredcites →https://doi.org/10.1093/nar/gks596openalex-snapshot

Primer3—new capabilities and interfaces

inferredcites →https://doi.org/10.1111/j.1365-2583.2006.00647.xopenalex-snapshot

Anopheles gambiae P450 reductase is highly expressed in oenocytes and in vivo knockdown increases permethrin susceptibility

inferredcites →https://doi.org/10.1111/j.1749-6632.1997.tb46178.xopenalex-snapshot

Insect Myosuppressins and Sulfakinins Stimulate Release of the Digestive Enzyme α‐Amylase in Two Invertebrates: The Scallop Pecten maximus and Insect Rhynchophorus ferrugineus

inferredcites →https://doi.org/10.1126/science.3749893openalex-snapshot

Leucosulfakinin, a Sulfated Insect Neuropeptide with Homology to Gastrin and Cholecystokinin

inferredcites →https://doi.org/10.1146/annurev.nutr.21.1.23openalex-snapshot

F AT M ETABOLISM IN I NSECTS

inferredcites →https://doi.org/10.1186/1471-2091-10-21openalex-snapshot

Contribution of oenocytes and pheromones to courtship behaviour in Drosophila

inferredcites →https://doi.org/10.1186/1471-2105-10-159openalex-snapshot

Transmembrane protein topology prediction using support vector machines

inferredcites →https://doi.org/10.1251/bpo20openalex-snapshot

Semiquantitative RT-PCR analysis to assess the expression levels of multiple transcripts from the same sample

inferredcites →https://doi.org/10.1371/journal.pone.0094502openalex-snapshot

Signaling Properties and Pharmacological Analysis of Two Sulfakinin Receptors from the Red Flour Beetle, Tribolium castaneum

inferredcites →https://doi.org/10.1590/s0074-02762011000300009openalex-snapshot

Insights into the transcriptome of oenocytes from Aedes aegypti pupae

inferredcites →https://doi.org/10.1673/031.010.14116openalex-snapshot

Identification of Myotropic Neuropeptides from the Brain and Corpus Cardiacum-Corpus Allatum Complex of the Beetle,Zophobas atratus

inferredcites →https://doi.org/10.2174/0929866526666190913142115openalex-snapshot

Sulfakinin Signalling Influences Fatty Acid Levels and Composition in Tenebrio Molitor Beetle

inferredcites →https://doi.org/10.2741/3510openalex-snapshot

Plasticity in the effects of sulfated and nonsulfated sulfakinin on heart contractions

inferredcites →https://doi.org/10.3389/fendo.2012.00109openalex-snapshot

Insulin-Producing Cells in the Drosophila Brain also Express Satiety-Inducing Cholecystokinin-Like Peptide, Drosulfakinin

inferredcites →https://doi.org/10.3389/fphys.2021.701203openalex-snapshot

Insulin-Like Peptides and Cross-Talk With Other Factors in the Regulation of Insect Metabolism

inferredcites →https://doi.org/10.3389/neuro.03.003.2007openalex-snapshot

The satiety signaling neuropeptide perisulfakinin inhibits the activity of central neurons promoting general activity

inferredcites →https://doi.org/10.3390/molecules24010017openalex-snapshot

Cholinergic Agonists and Antagonists Have an Effect on the Metabolism of the Beetle Tenebrio Molitor

inferredcites →https://doi.org/10.59674/pbkz40openalex-snapshot

Postępy Biologii Komórki

inferredcites →https://doi.org/10.7554/elife.58019openalex-snapshot

Isolation and transcriptomic analysis of Anopheles gambiae oenocytes enables the delineation of hydrocarbon biosynthesis

What points at this work

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

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Solanaceae Glycoalkaloids Disturb Lipid Homeostasis in Tenebrio Molitor Beetle

inferred← citeshttps://doi.org/10.1007/5584_2025_874openalex-snapshot

The Fat Body: Structure and Functions

inferred← citeshttps://doi.org/10.1007/978-3-032-04842-4_874openalex-snapshot

The Fat Body: Structure and Functions

inferred← citeshttps://doi.org/10.1007/s00018-022-04214-4openalex-snapshot

Cholecystokinin/sulfakinin peptide signaling: conserved roles at the intersection between feeding, mating and aggression

inferred← citeshttps://doi.org/10.1007/s11356-024-35099-4openalex-snapshot

A tomato a day keeps the beetle away – the impact of Solanaceae glycoalkaloids on energy management in the mealworm Tenebrio molitor

inferred← citeshttps://doi.org/10.1016/b978-0-443-23720-1.00004-6openalex-snapshot

Evolutionarily conserved roles of cholecystokinin signaling

inferred← citeshttps://doi.org/10.1016/j.cbpc.2024.110018openalex-snapshot

Modulation of the antioxidant system by glycoalkaloids in the beetle Tenebrio molitor L.

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.114951openalex-snapshot

Plant secondary metabolites as potential bioinsecticides? Study of the effects of plant-derived volatile organic compounds on the reproduction and behaviour of the pest beetle Tenebrio molitor

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120030openalex-snapshot

Bioimaging and distribution of unmodified and polyethylene glycol-modified up-converting SrF2:Yb3+,Er3+ nanoparticles in Tenebrio molitor larvae and their impact on lifespan, moulting, and metabolism

inferred← citeshttps://doi.org/10.1016/j.peptides.2026.171511openalex-snapshot

Sulfakinin neuropeptides and their receptors in insects: Molecular signalling, physiological diversity, and pest management implications

inferred← citeshttps://doi.org/10.1016/j.porgcoat.2026.110408openalex-snapshot

Corrosion inhibition of carbon steel using insect oil: Chemical characterization and long-term performance

inferred← citeshttps://doi.org/10.1021/acschemneuro.5c00053openalex-snapshot

Decoding Neuropeptide Complexity: Advancing Neurobiological Insights from Invertebrates to Vertebrates through Evolutionary Perspectives

inferred← citeshttps://doi.org/10.1186/s40659-025-00621-6openalex-snapshot

Metabolism dynamics in tropical cockroach during a cold-induced recovery period

inferred← citeshttps://doi.org/10.1186/s40659-025-00651-0openalex-snapshot

Insect neuropeptides as agents for pest control: potential and challenges

inferred← citeshttps://doi.org/10.2139/ssrn.6429008openalex-snapshot

Corrosion mitigation of carbon steel using insect oil: chemical characterization and long-term performance

inferred← citeshttps://doi.org/10.3390/metabo13121179openalex-snapshot

Solanaceae Glycoalkaloids Disturb Lipid Metabolism in the Tenebrio molitor Beetle

inferred← citeshttps://doi.org/10.3390/toxins18100410openalex-snapshot

Solasonine Modulates Aldose Reductase Activity in Galleria mellonella (Lepidoptera): Implications for the Polyol Pathway

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