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Research library — page 18

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RPEP-01009 · 2005

BNP and Endothelin Predict Different Types of Heart Failure Death: Sudden vs Progressive

NT-proBNP was the strongest predictor of progressive heart failure death, while endothelin-1 and norepinephrine better predicted sudden cardiac death — different neurohormones predict different death modes, enabling targeted prevention strategies (ICD vs medical intensification).

Berger, R; Huelsmann, M; Strecker, K; Moertl, D; Moser, P; Bojic, A; Pacher, R · Cohort

RPEP-01010 · 2005

BPC-157 Applied Locally Improves CO2 Laser Wound Healing in Mice

Local BPC-157 application accelerated CO2 laser wound healing in mice with faster re-epithelialization and wound contraction, extending BPC-157's documented wound healing to laser-induced tissue damage relevant to surgical and cosmetic dermatology.

Bilic, M; Bumber, Z; Blagaic, A Boban; Batelja, L; Seiwerth, S; Sikiric, P · Animal Study

RPEP-01011 · 2005

Gut Feeling: The Secret of Satiety and How Gut Hormones Control When You Stop Eating

Post-prandial gut hormones (GLP-1, PYY, CCK, oxyntomodulin) signal satiety through vagal and bloodstream pathways to brainstem/hypothalamic circuits, with combination peptide mimicry showing greater satiety than single agents — the future of appetite pharmacology.

Bloom, Steve; Wynne, Katie; Chaudhri, Owais · Review

RPEP-01012 · 2005

BPC-157 Effectively Treats Serotonin Syndrome in Rats

BPC-157 effectively counteracted serotonin syndrome signs (hyperthermia, tremor, rigidity, agitation) induced by multiple serotonergic drugs in rats, demonstrating serotonergic system modulation complementing its known dopaminergic and GABAergic interactions.

Boban Blagaic, Alenka; Blagaic, Vladimir; Mirt, Mirela; Jelovac, Nikola; Dodig, Goran; Rucman, Rudolf; Petek, Marijan; Turkovic, Branko; Anic, Tomislav; Dubovecak, Miroslav; Staresinic, Mario; Seiwerth, Sven; Sikiric, Predrag · Animal Study

RPEP-01015 · 2005

CCK and GLP-1 Together: Additive Appetite Suppression From Combining Two Gut Satiety Signals

Combined CCK and GLP-1 infusion produced additive effects on appetite suppression and antropyloroduodenal motility in healthy humans — supporting combination gut peptide therapy for superior satiety and weight management.

Brennan, Ixchel M; Feltrin, Kate L; Horowitz, Michael; Smout, Andre J P M; Meyer, James H; Wishart, Judith; Feinle-Bisset, Christine · RCT

RPEP-01016 · 2005

How Antimicrobial Peptides Kill Bacteria: It's Not Just About Making Holes

Antimicrobial peptides kill bacteria through more mechanisms than just punching holes in membranes. While three classic pore-forming models exist — 'barrel-stave,' 'carpet,' and 'toroidal-pore' — growing evidence shows that many peptides can also cross into bacterial cells and inhibit internal processes including cell wall synthesis, nucleic acid synthesis, protein synthesis, enzymatic activity, and membrane septum formation during cell division.

Brogden, Kim A ·

RPEP-01018 · 2005

Hexarelin Protects Newborn Brain From Injury Through Akt/GSK-3β Survival Signaling

Hexarelin reduced neonatal brain injury in a hypoxia-ischemia model and altered Akt/GSK-3β phosphorylation — activating pro-survival signaling cascades for direct GH-independent neuroprotection in the developing brain.

Brywe, Katarina G; Leverin, Anna-Lena; Gustavsson, Malin; Mallard, Carina; Granata, Riccarda; Destefanis, Silvia; Volante, Marco; Hagberg, Henrik; Ghigo, Ezio; Isgaard, Jörgen · Animal Study

RPEP-01019 · 2005

Morphine Changes the Body's Opioid Peptide Production at Sites of Inflammation

Morphine modified proopiomelanocortin and prodynorphin system activity in immune cells during zymosan-induced peritonitis, demonstrating that exogenous opioid drugs alter the endogenous opioid-immune pain control system at inflammation sites.

Chadzinska, M; Starowicz, K; Scislowska-Czarnecka, A; Bilecki, W; Pierzchala-Koziec, K; Przewlocki, R; Przewlocka, B; Plytycz, B · Animal Study

RPEP-01020 · 2005

Producing Thymosin Alpha-1 in Yeast: A Scalable Manufacturing System for This Immune Peptide

Recombinant thymosin alpha-1 produced in Pichia pastoris yeast expression system showed biological activity equivalent to chemically synthesized peptide, establishing a cost-effective, scalable manufacturing platform for clinical-grade thymosin alpha-1.

Chen, Feng; Chen, Xiang-Ming; Chen, Zhi; Jiang, Han-Liang; Pan, Xiao-Ping; Hu, Zhong-Rong; Liu, Rong-Hua; Chen, Xiao-Ming · In Vitro

RPEP-01021 · 2005

Thymosin Alpha-1 Works When Taken Orally — Immune Enhancement Without Injection

Oral thymosin alpha-1 enhanced T-cell function, NK cell activity, and cytokine production in mice, demonstrating that the peptide retains immunomodulatory activity after oral administration — a practical advance for non-injectable immune therapy.

Chen, Xiang-Ming; Jiang, Han-Liang; Zhou, Lin-Fu; Pan, Xiao-Ping; Hu, Zhong-Rong; Liu, Rong-Hua; Chen, Xiao-Ming; Chen, Zhi · Animal Study

RPEP-01022 · 2005

GH-Releasing Peptides and Bone: Direct Skeletal Effects Beyond GH-Mediated Growth

GH-releasing peptides affect bone metabolism through both indirect GH/IGF-1 stimulation and direct ghrelin receptor activation on osteoblasts, promoting bone formation through dual systemic and local mechanisms for potential osteoporosis therapy.

Cocchi, D; Maccarinelli, G; Sibilia, V; Tulipano, G; Torsello, A; Pazzaglia, U E; Giustina, A; Netti, C · Review

RPEP-01024 · 2005

Ghrelin and PYY Levels in Obesity From Brain Damage: Hypothalamic Obesity Hormones

Patients with acquired structural hypothalamic damage-induced obesity had elevated ghrelin and reduced PYY3-36 compared to matched controls, suggesting specific gut peptide dysregulation contributes to hypothalamic obesity beyond central appetite circuit damage.

Daousi, Christina; MacFarlane, Ian A; English, Patrick J; Wilding, John P H; Patterson, Michael; Dovey, Terence M; Halford, Jason C G; Ghatei, Mohammad A; Pinkney, Jonathan H · Cross Sectional

RPEP-01025 · 2005

Computer Models Predict Which Peptide Sequences Will Kill Bacteria

A stochastic computational approach (extended MARCH-INSIDE) accurately predicted antimicrobial activity of lactoferrin-derived and other peptides based on sequence descriptors, validating computational methods for rational antimicrobial peptide design.

de Armas, Ronal Ramos; Díaz, Humberto González; Molina, Reinaldo; Uriarte, Eugenio · In Vitro

RPEP-01026 · 2005

Ghrelin, GHRP-6, and Motilin: Comparing Their Gut Motility Effects Head-to-Head

Ghrelin and GHRP-6 stimulated gastric motility in rats through both GHS-R and motilin receptor cross-activation, with efficacy comparable to motilin — confirming the bidirectional receptor overlap drives GH secretagogue gut motility effects.

Depoortere, Inge; De Winter, Benedicte; Thijs, Theo; De Man, Joris; Pelckmans, Paul; Peeters, Theo · Animal Study

RPEP-01027 · 2005

Obese People Have Delayed Stomach Emptying But Higher CCK and PYY — A Satiety Paradox

Morbidly obese patients had delayed gastric emptying, impaired gallbladder contraction, yet elevated CCK and PYY3-36 levels — a paradox suggesting gut satiety signal resistance in obesity, analogous to leptin resistance.

Di Francesco, Vincenzo; Zamboni, Mauro; Dioli, Andrea; Zoico, Elena; Mazzali, Gloria; Omizzolo, Francesca; Bissoli, Luisa; Solerte, Sebastiano B; Benini, Luigi; Bosello, Ottavio · Cross Sectional

RPEP-01028 · 2005

Combining Low-Dose PT-141 Nasal Spray With Viagra: Synergistic Erectile Effect

Co-administration of low-dose intranasal PT-141 (melanocortin agonist) with sildenafil (PDE5 inhibitor) produced synergistic erectile responses in ED patients — combining central desire/arousal with peripheral vasodilation for superior outcomes.

Diamond, L E; Earle, D C; Garcia, W D; Spana, C · RCT

RPEP-01030 · 2005

Two Forms of CCK Suppress Appetite Through the Same Liver Nerve Pathway

Both CCK-8 and CCK-33 reduced food intake through hepatic branch vagal afferents in rats, but CCK-33 produced more sustained satiety — demonstrating shared pathway with temporal differences between CCK molecular forms.

Eisen, S; Phillips, R J; Geary, N; Baronowsky, E A; Powley, T L; Smith, G P · Animal Study

RPEP-01032 · 2005

How Tasty Food Breaks Your Appetite Control: Opioid, GLP-1, and Ghrelin Disruption

Palatable food disrupts appetite regulation through opioid reward pathway overactivation (hedonic eating), blunted satiety peptide responses (GLP-1, PYY, CCK), and altered ghrelin dynamics — creating a multi-level biological mechanism for food addiction and overconsumption.

Erlanson-Albertsson, Charlotte · Review

RPEP-01038 · 2005

GHRP-2 Reduces Arthritis Inflammation: A GH Secretagogue as an Anti-Inflammatory Drug

GHRP-2 reduced clinical arthritis scores, joint inflammation, and cartilage destruction in adjuvant-arthritic rats, suppressing pro-inflammatory cytokines (TNF-α, IL-6) — establishing GH secretagogues as anti-inflammatory agents for arthritis treatment.

Granado, Miriam; Priego, Teresa; Martín, Ana I; Villanúa, M Angeles; López-Calderón, Asunción · Animal Study

RPEP-01039 · 2005

CRF Peptide Family in Inflammation: Beyond Stress to Peripheral Immune Regulation

CRF family peptides (CRF, urocortin 1-3) modulate peripheral inflammation through CRF1 (generally pro-inflammatory) and CRF2 (generally anti-inflammatory) receptors on immune cells, gut, and skin — with therapeutic applications for IBD, arthritis, and dermatitis.

Gravanis, Achille; Margioris, Andrew N · Review

RPEP-01040 · 2005

sGP130 and BNP Predict Different Heart Failure Progression Patterns Over Years

Soluble GP130 (IL-6 trans-signaling marker) and NT-proBNP both predicted heart failure progression over 2+ years but reflected different pathophysiology: GP130 = inflammatory deterioration; BNP = hemodynamic stress — complementary long-term prognostic markers.

Gwechenberger, Marianne; Pacher, Richard; Berger, Rudolf; Zorn, Gerlinde; Moser, Petra; Stanek, Brigitte; Huelsmann, Martin · Cohort

RPEP-01041 · 2005

The Accidental Discovery That a Tanning Peptide Enhances Sexual Function in Both Sexes

Melanotan II, a synthetic melanocortin analog originally studied for skin tanning, was found to enhance erectile function in men and increase sexual desire and genital arousal in women. The peptide's mechanism of action is fundamentally different from PDE5 inhibitors like Viagra — it works centrally through melanocortin receptors in the brain rather than peripherally on blood vessels, producing what the author characterizes as a more natural sexual response with minimal side effects. The sexual effects were discovered accidentally during human skin pigmentation studies, representing a classic example of serendipity in drug discovery.

Hadley, Mac E ·

RPEP-01042 · 2005

PYY3-36 Causes Taste Aversion at Appetite-Suppressing Doses — A Nausea Concern

Peripheral PYY3-36 at appetite-suppressing doses produced conditioned taste aversion (learned food avoidance suggesting nausea), indicating its anorectic effect may partly involve malaise rather than pure satiety — an important consideration for PYY-based obesity drugs.

Halatchev, Ilia G; Cone, Roger D · Animal Study

RPEP-01043 · 2005

A Ghrelin Receptor Antagonist That Blocks GH But Paradoxically Increases Appetite

A novel GHS-R1a antagonist blocked ghrelin-induced GH release but paradoxically increased food intake, suggesting inverse agonism or biased antagonism at the constitutively active receptor — complex pharmacology where blocking one ghrelin function doesn't block another.

Halem, Heather A; Taylor, John E; Dong, Jesse Z; Shen, Yeelana; Datta, Rakesh; Abizaid, Alfonso; Diano, Sabrina; Horvath, Tamas L; Culler, Michael D · Animal Study

RPEP-01046 · 2005

The Endogenous Opioid System and Clinical Pain Management: A Practical Guide

The endogenous opioid system (endorphins, enkephalins, dynorphins) provides the biological foundation for clinical pain management: understanding endogenous analgesia mechanisms improves opioid drug selection, dosing, and integration with non-pharmacological approaches.

Holden, Janean E; Jeong, Younhee; Forrest, Jeannine M · Review

RPEP-01047 · 2005

GH Secretagogues Act as Both Ghrelin Agonists and Allosteric Receptor Modulators

MK-677, hexarelin, and other GH secretagogues demonstrated both direct GHS-R agonism and allosteric modulation of ghrelin binding — some enhancing (positive) and others reducing (negative) ghrelin's own receptor interaction, revealing complex biased pharmacology.

Holst, Birgitte; Brandt, Erik; Bach, Anders; Heding, Anders; Schwartz, Thue W · In Vitro

RPEP-01048 · 2005

Human Lactoferricin's Structure: Partially Folded in Water, Fully Active at Membranes

NMR studies showed human lactoferricin adopts a partially structured conformation in water that stabilizes into an amphipathic beta-hairpin at membrane-mimetic surfaces, revealing that the bacterial membrane itself activates the peptide's antimicrobial structure.

Hunter, Howard N; Demcoe, A Ross; Jenssen, Håvard; Gutteberg, Tore J; Vogel, Hans J · In Vitro

RPEP-01049 · 2005

Cathelicidin Is Essential for Protecting Your Colon Against Bacterial Infection

Mice lacking the cathelicidin gene (Cnlp-/-) were dramatically more vulnerable to intestinal infection than normal mice. When infected with Citrobacter rodentium — a pathogen that mimics dangerous human E. coli strains — cathelicidin-deficient mice developed significantly greater colon colonization, epithelial cell damage, and systemic spread of infection. Normal mice were protected from infection doses that reliably infected the knockout mice. The study also showed that cathelicidin (mCRAMP) expression in the gut is concentrated in the colon's surface epithelial cells, and that colon cell extracts from normal mice killed C. rodentium significantly better than extracts from cathelicidin-deficient mice.

Iimura, Mitsutoshi; Gallo, Richard L; Hase, Koji; Miyamoto, Yukiko; Eckmann, Lars; Kagnoff, Martin F · Animal Study

RPEP-01055 · 2005

Oxytocin Calms the Brain's Fear Center: Neural Imaging Reveals the Anti-Anxiety Mechanism

Intranasal oxytocin attenuated amygdala reactivity to threatening facial expressions measured by fMRI in healthy humans, providing the first neural imaging evidence for oxytocin's anxiolytic mechanism through direct fear-circuit modulation.

Kirsch, Peter; Esslinger, Christine; Chen, Qiang; Mier, Daniela; Lis, Stefanie; Siddhanti, Sarina; Gruppe, Harald; Mattay, Venkata S; Gallhofer, Bernd; Meyer-Lindenberg, Andreas · RCT

RPEP-01057 · 2005

Bulimia Nervosa Patients Have Abnormal Ghrelin and PYY Responses to Meals

Bulimia nervosa patients demonstrated blunted post-meal ghrelin suppression and altered PYY3-36 response compared to healthy controls, indicating disrupted gut peptide satiety signaling that may perpetuate the binge-purge cycle.

Kojima, Shinya; Nakahara, Toshihiro; Nagai, Nobuatsu; Muranaga, Tetsuro; Tanaka, Muneki; Yasuhara, Daisuke; Masuda, Akinori; Date, Yukari; Ueno, Hiroaki; Nakazato, Masamitsu; Naruo, Tetsuro · Clinical Trial

RPEP-01058 · 2005

Oxytocin Increases Trust in Humans: The Landmark Nasal Spray Experiment

Intranasal oxytocin caused a substantial increase in trust behavior during a trust game, where participants had to decide how much money to entrust to an anonymous partner who could either reciprocate or keep it all. Critically, the study demonstrated that oxytocin's effect was specific to social trust — it increased willingness to accept risks arising from interpersonal interactions, but did not increase general risk tolerance. This distinction suggests oxytocin targets the neural circuits involved in social approach behavior rather than simply reducing fear or caution across the board.

Kosfeld, Michael; Heinrichs, Markus; Zak, Paul J; Fischbacher, Urs; Fehr, Ernst ·

RPEP-01061 · 2005

Ghrelin: Is It an Active Player in Disease or Just a Bystander Biomarker?

Ghrelin changes in various disease states (cardiovascular, inflammatory, GI, metabolic) likely represent active physiological responses with functional consequences, not passive biomarker changes — supporting therapeutic ghrelin modulation in disease.

Lago, Francisca; Gonzalez-Juanatey, José Ramón; Casanueva, Felipe F; Gómez-Reino, Juan; Dieguez, Carlos; Gualillo, Oreste · Review

RPEP-01064 · 2005

BPC-157 Heals Corneal Defects: Eye Wound Healing From a Gut Peptide

BPC-157 accelerated corneal epithelial defect healing in rats with faster re-epithelialization compared to controls, extending its documented tissue repair capabilities to the eye — a new organ system for BPC-157 therapeutic application.

Lazić, Ratimir; Gabrić, Nikica; Dekaris, Iva; Bosnar, Damir; Boban-Blagaić, Alenka; Sikirić, Predrag · Animal Study

RPEP-01065 · 2005

DMP696 and DMP904: Two CRF1 Antagonists With Distinct Pharmacological Profiles for Anxiety

DMP696 and DMP904 demonstrated CRF1 receptor antagonist anxiolytic activity with distinct pharmacokinetic, selectivity, and efficacy profiles across anxiety models — advancing multiple CRF1 drug candidates with different clinical potential.

Li, Yu-Wen; Fitzgerald, Lawrence; Wong, Harvey; Lelas, Snjezana; Zhang, Ge; Lindner, Mark D; Wallace, Tanya; McElroy, John; Lodge, Nicholas J; Gilligan, Paul; Zaczek, Robert · Review

RPEP-01067 · 2005

Lactoferricin Selectively Kills Cancer Cells While Sparing Normal Cells

Bovine lactoferricin induced apoptosis selectively in human leukemia (Jurkat, CEM) and carcinoma (MDA-MB-435) cell lines while sparing normal lymphocytes and fibroblasts — demonstrating cancer-selective cytotoxicity through membrane-dependent mechanisms.

Mader, Jamie S; Salsman, Jayme; Conrad, David M; Hoskin, David W · In Vitro

RPEP-01068 · 2005

Urotensin II Inversely Correlates With Sympathetic Activity and BNP in Kidney Failure

Plasma urotensin II inversely correlated with muscle sympathetic nerve activity and cardiac natriuretic peptides in ESRD patients, suggesting urotensin II serves a counter-regulatory role in the sympathetic-peptide axis in cardiorenal disease.

Mallamaci, Francesca; Cutrupi, Sebastiano; Pizzini, Patrizia; Tripepi, Giovanni; Zoccali, Carmine · Cross Sectional

RPEP-01069 · 2005

Milk Peptides Lower Blood Pressure by Up to 10 mmHg in Placebo-Controlled Trial

Milk-derived peptides VPP and IPP — natural ACE inhibitors from casein — lowered systolic blood pressure in a dose-dependent manner over 6 weeks. The highest dose (3.6 mg VPP+IPP daily) produced a 10.1 mmHg decrease in systolic blood pressure, significantly better than placebo (p<0.001). Even the lowest active dose (1.8 mg) produced a significant 6.3 mmHg reduction at 6 weeks. The blood pressure changes were: placebo −1.7 mmHg, 1.8 mg −6.3 mmHg, 2.5 mg −6.7 mmHg, and 3.6 mg −10.1 mmHg. The effect was stronger in mildly hypertensive subjects. Diastolic blood pressure was not significantly affected.

Mizuno, Seiichi; Matsuura, Keiichi; Gotou, Takanobu; Nishimura, Shingo; Kajimoto, Osami; Yabune, Mitsuharu; Kajimoto, Yoshitaka; Yamamoto, Naoyuki · Randomized Controlled Trial (Single Blind)