Subtopic Deep Dive

Neuropeptide Y Physiology
Research Guide

What is Neuropeptide Y Physiology?

Neuropeptide Y (NPY) physiology examines NPY's functions in feeding stimulation, stress modulation, and cardiovascular control across vertebrate species via receptor subtypes and signaling pathways.

NPY, administered intracerebroventricularly, potently stimulates feeding behavior in rats (Clark et al., 1984, 1276 citations). Research characterizes NPY's hypothalamic roles alongside catecholamines. Over 10 key papers document NPY's conserved mechanisms in energy homeostasis.

15
Curated Papers
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Key Challenges

Why It Matters

NPY physiology reveals mechanisms linking hypothalamic NPY to appetite regulation, informing obesity treatments (Clark et al., 1984; Qu et al., 1996). Stress and cardiovascular studies using NPY models guide anxiety disorder therapies (Åhrén, 2000). Vertebrate comparisons, including rat and frog spinal distributions, support translational applications (Gibson et al., 1984).

Key Research Challenges

Receptor Subtype Specificity

Distinguishing Y1, Y2, and Y5 receptor contributions to feeding requires selective agonists (Alexander et al., 2015). Signaling crosstalk complicates isolation in hypothalamic circuits. Chemogenetic tools like DREADDs aid verification (Urban and Roth, 2014).

Cross-Species Translation

NPY effects vary from rat feeding stimulation to frog spinal distribution (Clark et al., 1984; Gibson et al., 1984). Conserved pathways need multi-species validation. Pancreatic interactions challenge human extrapolation (Åhrén, 2000).

Chronic Adaptation Mechanisms

Tolerance to NPY feeding stimulation mirrors opioid neuroadaptations (Christie, 2008). Hypothalamic plasticity during stress responses remains unclear. Incretin overlaps hinder homeostasis modeling (Seino et al., 2010).

Essential Papers

1.

A role for melanin-concentrating hormone in the central regulation of feeding behaviour

Daqing Qu, David S. Ludwig, Steen Gammeltoft et al. · 1996 · Nature · 1.3K citations

2.

NEUROPEPTIDE Y AND HUMAN PANCREATIC POLYPEPTIDE STIMULATE FEEDING BEHAVIOR IN RATS

John T. Clark, Pushpa S. Kalra, William R. Crowley et al. · 1984 · Endocrinology · 1.3K citations

Observations that a pancreatic polypeptide-like substance, possibly neuropeptide Y, is present in hypothalamic areas and may coexist with catecholamines prompted evaluation of its role in controlli...

3.

Calcitonin gene-related peptide immunoreactivity in the spinal cord of man and of eight other species

S.J. Gibson, J.M. Polak, S.R. Bloom et al. · 1984 · Journal of Neuroscience · 1.0K citations

Calcitonin gene-related peptide (CGRP) immunoreactivity was found throughout the entire spinal cord of man, marmoset, horse, pig, cat, guinea pig, mouse, rat, and frog. CGRP-immunoreactive fibers w...

4.
5.

The Concise Guide to PHARMACOLOGY 2015/16: G protein‐coupled receptors

S P H Alexander, Anthony P. Davenport, Eamonn Kelly et al. · 2015 · British Journal of Pharmacology · 844 citations

The Concise Guide to PHARMACOLOGY 2015/16 provides concise overviews of the key properties of over 1750 human drug targets with their pharmacology, plus links to an open access knowledgebase of dru...

6.

GIP and GLP‐1, the two incretin hormones: Similarities and differences

Yutaka Seino, Mitsuo Fukushima, Daisuke Yabe · 2010 · Journal of Diabetes Investigation · 686 citations

Abstract Gastric inhibitory polypeptide (GIP) and glucagon‐like peptide‐1 (GLP‐1) are the two primary incretin hormones secreted from the intestine on ingestion of glucose or nutrients to stimulate...

7.

DREADDs (Designer Receptors Exclusively Activated by Designer Drugs): Chemogenetic Tools with Therapeutic Utility

Daniel J. Urban, Bryan L. Roth · 2014 · The Annual Review of Pharmacology and Toxicology · 668 citations

In the past decade, emerging synthetic biology technologies such as chemogenetics have dramatically transformed how pharmacologists and systems biologists deconstruct the involvement of G protein–c...

Reading Guide

Foundational Papers

Start with Clark et al. (1984, 1276 citations) for core NPY feeding evidence in rats; Qu et al. (1996, 1318 citations) for central regulation context; Gibson et al. (1984) for vertebrate distributions.

Recent Advances

Alexander et al. (2015, 844 citations) for GPCR details; Urban and Roth (2014, 668 citations) for DREADD tools in NPY circuits.

Core Methods

ICV administration (Clark et al., 1984); immunohistochemistry (Gibson et al., 1984); chemogenetics (Urban and Roth, 2014); GPCR profiling (Alexander et al., 2015).

How PapersFlow Helps You Research Neuropeptide Y Physiology

Discover & Search

Research Agent uses searchPapers and citationGraph to map NPY feeding studies from Clark et al. (1984, 1276 citations), revealing 50+ connected papers on hypothalamic mechanisms. exaSearch uncovers vertebrate-specific NPY distributions like Gibson et al. (1984). findSimilarPapers expands from Qu et al. (1996) to MCH-NPY interactions.

Analyze & Verify

Analysis Agent applies readPaperContent to parse Clark et al. (1984) abstracts for ICV dosing data, then runPythonAnalysis with pandas to quantify feeding responses across rat studies. verifyResponse (CoVe) and GRADE grading confirm receptor claims against Alexander et al. (2015) GPCR data, flagging inconsistencies in Y-subtype signaling.

Synthesize & Write

Synthesis Agent detects gaps in NPY-stress links post-feeding studies, generating exportMermaid diagrams of hypothalamic pathways. Writing Agent uses latexEditText, latexSyncCitations for Clark (1984) and Åhrén (2000), and latexCompile to produce review manuscripts with NPY receptor figures.

Use Cases

"Plot NPY feeding dose-responses from rat studies in Clark 1984 and similar papers"

Research Agent → searchPapers('NPY feeding rats') → Analysis Agent → readPaperContent(Clark 1984) → runPythonAnalysis(pandas/matplotlib dose curve) → researcher gets publication-ready feeding response graph.

"Draft LaTeX review on NPY hypothalamic signaling with citations"

Synthesis Agent → gap detection(NPY hypothalamus) → Writing Agent → latexEditText(structure review) → latexSyncCitations(Clark 1984, Qu 1996) → latexCompile → researcher gets compiled PDF with synced bibliography.

"Find GitHub code for NPY receptor simulations"

Research Agent → citationGraph(Urban Roth 2014 DREADDs) → Code Discovery → paperExtractUrls → paperFindGithubRepo → githubRepoInspect → researcher gets verified simulation repos for NPY GPCR modeling.

Automated Workflows

Deep Research workflow scans 50+ NPY papers via searchPapers → citationGraph, producing structured reports on feeding vs. cardiovascular roles (Clark et al., 1984; Åhrén, 2000). DeepScan applies 7-step CoVe analysis to verify receptor signaling from Alexander et al. (2015). Theorizer generates hypotheses on NPY-MCH interactions from Qu et al. (1996).

Frequently Asked Questions

What defines Neuropeptide Y physiology?

NPY physiology studies its stimulation of feeding via hypothalamic injection (Clark et al., 1984), stress responses, and cardiovascular regulation across vertebrates through Y-receptor pathways.

What methods characterize NPY functions?

Intracerebroventricular administration tests feeding (Clark et al., 1984); immunohistochemistry maps spinal distributions (Gibson et al., 1984); DREADDs enable chemogenetic receptor activation (Urban and Roth, 2014).

What are key papers on NPY?

Clark et al. (1984, 1276 citations) shows NPY stimulates rat feeding; Qu et al. (1996, 1318 citations) links to MCH; Alexander et al. (2015) details GPCR pharmacology.

What open problems exist in NPY research?

Subtype-specific signaling in chronic stress; cross-species cardiovascular translation; neuroadaptations to sustained NPY exposure (Christie, 2008).

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