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Research library — page 10

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RPEP-00519 · 1999

3D Structure of a Plant Peptide That Inhibits HIV Reveals How It Works

Circulin A's 3D structure reveals a cyclic cystine knot fold with exposed hydrophobic and positively charged surface patches, providing a structural basis for its membrane-disrupting anti-HIV activity.

Daly, N L; Koltay, A; Gustafson, K R; Boyd, M R; Casas-Finet, J R; Craik, D J · In Vitro

RPEP-00522 · 1999

Growth Hormone Peptides Do More Than Release GH: Cardiovascular, Appetite, and Sleep Effects

GH secretagogues have clinically significant non-endocrine effects including cardiovascular protection, orexigenic (appetite-stimulating) activity, sleep architecture improvement, and potential anti-aging properties mediated by widespread GHS receptor distribution.

Ghigo, E; Arvat, E; Broglio, F; Giordano, R; Gianotti, L; Muccioli, G; Papotti, M; Graziani, A; Bisi, G; Deghenghi, R; Camanni, F · Review

RPEP-00524 · 1999

How Thymus Peptides Connect the Immune System, Hormones, and Aging

The thymic-pituitary axis forms a bidirectional neuroendocrine circuit that deteriorates with age, contributing to immunosenescence. Thymic peptide supplementation may restore immune-endocrine homeostasis in aging.

Goya, R G; Bolognani, F · Review

RPEP-00525 · 1999

Evidence That Aging Disrupts the Thymus-Pituitary Hormone Connection

Aging causes progressive disruption of the pituitary-thymic bidirectional circuit: reduced thymic peptide production, altered pituitary hormone output, and impaired integration between immune and endocrine systems, creating a self-reinforcing decline.

Goya, R G; Brown, O A; Bolognani, F · Review

RPEP-00526 · 1999

Oral GHRP-2 Successfully Releases Growth Hormone in Young Goats

Oral GHRP-2 (5-10 mg/kg) stimulated significant GH release in 1-month-old goats (peak at 15 min) but not in 3-month-old goats, demonstrating age-dependent oral peptide bioavailability in ruminants.

Hashizume, T; Kawai, M; Ohtsuki, K; Ishii, A; Numata, M · Animal Study

RPEP-00529 · 1999

BPC-157 Prevents Tolerance and Physical Dependence From Chronic Diazepam Use in Rats

BPC-157 co-administration with chronic diazepam (10 days) prevented tolerance development, maintained anticonvulsant efficacy, and reduced withdrawal seizure severity at both 10 μg/kg and 10 ng/kg doses in rats.

Jelovac, N; Sikiric, P; Rucman, R; Petek, M; Perovic, D; Marovic, A; Anic, T; Seiwerth, S; Mise, S; Pigac, B; Duplancie, B; Turkovic, B; Dodig, G; Prkacin, I; Stancic-Rokotov, D; Zoricic, I; Aralica, G; Sebecic, B; Ziger, T; Slobodnjak, Z · Animal Study

RPEP-00530 · 1999

Ipamorelin Increases Bone Growth Rate in a Dose-Dependent Manner in Rats

Ipamorelin (18-450 μg/day SC, three daily injections for 15 days) increased longitudinal bone growth rate and body weight dose-dependently in rats, with sustained GH release throughout the treatment period.

Johansen, P B; Nowak, J; Skjaerbaek, C; Flyvbjerg, A; Andreassen, T T; Wilken, M; Orskov, H · Animal Study

RPEP-00537 · 1999

Thymosin Beta-4 Accelerates Wound Healing by Up to 61% in Rats

Thymosin beta-4 (Tβ4) applied topically or intraperitoneally to full-thickness wounds in rats accelerated skin regrowth by 42% at day 4 and up to 61% at day 7 compared to saline controls. Treated wounds also contracted at least 11% more than controls by day 7. The peptide increased collagen deposition and new blood vessel formation in the wound. In lab assays, thymosin beta-4 stimulated keratinocyte (skin cell) migration 2–3-fold at doses as low as 10 picograms — an extraordinarily small amount.

Malinda, K M; Sidhu, G S; Mani, H; Banaudha, K; Maheshwari, R K; Goldstein, A L; Kleinman, H K ·

RPEP-00539 · 1999

Designing Circular Peptide Drugs That Block HIV Protease

High-resolution crystal structures of seven macrocyclic HIV protease inhibitors revealed specific binding interactions, demonstrating how cyclic peptide scaffolds can achieve potent enzyme inhibition with improved drug properties.

Martin, J L; Begun, J; Schindeler, A; Wickramasinghe, W A; Alewood, D; Alewood, P F; Bergman, D A; Brinkworth, R I; Abbenante, G; March, D R; Reid, R C; Fairlie, D P · In Vitro

RPEP-00541 · 1999

GHRP-2 Maintains Growth Hormone Release in Children Taking Prednisone

GHRP-2 preserved GH secretory response in 8 children during prednisone therapy, maintaining GH release levels comparable to pre-treatment baseline, suggesting GHRP-2 bypasses glucocorticoid-induced somatostatin excess.

Meacham, L R; Culler, F L; Abdul-Latif, H; Sullivan, K M; Bowers, C Y · Clinical Trial

RPEP-00543 · 1999

How Your Body Activates Peptide Hormones: The Enzymes PC1 and PC2 Explained

PC1 and PC2 follow markedly different activation pathways. PC1 undergoes rapid propeptide cleavage in the endoplasmic reticulum and is further activated by a carboxyl-terminal processing event. PC2, by contrast, has much longer folding times, exits the ER without propeptide cleavage, and requires association with the neuroendocrine-specific protein 7B2 to become catalytically active. The 7B2 protein is internally cleaved into a 21-kDa fragment and a 31-residue carboxy-terminal peptide once the complex reaches the trans-Golgi network. PC2 propeptide removal occurs later in secretory granules, likely through autocatalysis, but without prior 7B2 encounter, PC2 cannot generate an active enzyme. A 36-residue internal segment of 7B2 appears to mediate the critical conformational changes.

Muller, L; Lindberg, I · Review

RPEP-00551 · 1999

BPC-157 Protects the Stomach From Damage Caused by the Diabetes Drug Alloxan

BPC-157 significantly attenuated alloxan-induced gastric lesions in rats (200 mg/kg SC) and mice (400 mg/kg IP), reducing lesion severity and accelerating healing over the observation period.

Petek, M; Sikiric, P; Anic, T; Buljat, G; Separovic, J; Stancic-Rokotov, D; Seiwerth, S; Grabarevic, Z; Rucman, R; Mikus, D; Zoricic, I; Prkacin, I; Sebecic, B; Ziger, T; Coric, V; Turkovic, B; Aralica, G; Rotkvic, I; Mise, S; Hahn, V · Animal Study

RPEP-00552 · 1999

Sermorelin for Children with Growth Hormone Deficiency: Diagnosis and Treatment Review

Sermorelin, a 29-amino-acid synthetic GHRH analog, serves two clinical roles in children: as a diagnostic test for growth hormone deficiency (via single IV dose of 1 μg/kg) and as a treatment (via daily subcutaneous injection of 30 μg/kg at bedtime). As a diagnostic tool, it produced fewer false positives than other provocative tests. As a treatment, it significantly increased height velocity sustained over 12 months, with limited data suggesting benefits persist through 36 months. However, sermorelin cannot detect hypothalamic-origin GH deficiency (since it acts at the pituitary level), and its growth-promoting effects appear somewhat less robust than direct growth hormone (somatropin) therapy at equivalent doses.

Prakash, A; Goa, K L · Review

RPEP-00554 · 1999

How Oral MK-677 Increases IGF-1: Direct GH Stimulation Plus Independent Mechanisms in Dogs

MK-677 increased IGF-1 through both GH-dependent and GH-independent mechanisms, and elevated cortisol through direct adrenal stimulation rather than ACTH, revealing multi-target pharmacology beyond simple GH secretagogue activity.

Schleim, K D; Jacks, T; Cunningham, P; Feeney, W; Frazier, E G; Niebauer, G W; Zhang, D; Chen, H; Smith, R G; Hickey, G · Animal Study

RPEP-00555 · 1999

BPC-157 Heals Bone Defects in Rabbits as Effectively as Growth Factors

BPC-157 promoted segmental bone defect healing in rabbits with osteogenic activity comparable to IGF-1 and TGF-beta, demonstrating significant bone regeneration through angiogenic and osteoblast-stimulating mechanisms.

Sebecić, B; Nikolić, V; Sikirić, P; Seiwerth, S; Sosa, T; Patrlj, L; Grabarević, Z; Rucman, R; Petek, M; Konjevoda, P; Jadrijević, S; Perović, D; Slaj, M · Animal Study

RPEP-00558 · 1999

BPC-157 Shows Protective Effects in Mouse Models of Parkinson's Disease

BPC-157 attenuated both MPTP- and haloperidol-induced Parkinson's-like symptoms in mice while simultaneously protecting against gastric lesions caused by these parkinsongenic agents.

Sikiric, P; Marovic, A; Matoz, W; Anic, T; Buljat, G; Mikus, D; Stancic-Rokotov, D; Separovic, J; Seiwerth, S; Grabarevic, Z; Rucman, R; Petek, M; Ziger, T; Sebecic, B; Zoricic, I; Turkovic, B; Aralica, G; Perovic, D; Duplancic, B; Lovric-Bencic, M; Rotkvic, I; Mise, S; Jagic, V; Hahn, V · Animal Study

RPEP-00559 · 1999

BPC-157's Stomach Protection Lasts Long After the Drug Is Gone

BPC-157 provided long-lasting cytoprotection lasting days after administration in gastrectomized rats with duodenal ulcers and reflux esophagitis, significantly outlasting ranitidine and sucralfate.

Sikiric, P; Jadrijevic, S; Seiwerth, S; Sosa, T; Deskovic, S; Perovic, D; Aralica, G; Grabarevic, Z; Rucman, R; Petek, M; Jagic, V; Turkovic, B; Ziger, T; Rotkvic, I; Mise, S; Zoricic, I; Sebecic, B; Patrlj, L; Kocman, B; Sarlija, M; Mikus, D; Separovic, J; Hanzevacki, M; Gjurasin, M; Miklic, P · Animal Study

RPEP-00560 · 1999

BPC-157 Promotes New Blood Vessel and Tissue Growth Better Than Standard Ulcer Drugs

BPC-157 promoted significantly more angiogenesis and granulation tissue formation than H2-blockers, omeprazole, or sucralfate, identifying its primary healing mechanism as enhanced new tissue growth rather than acid suppression.

Sikiric, P; Separovic, J; Anic, T; Buljat, G; Mikus, D; Seiwerth, S; Grabarevic, Z; Stancic-Rokotov, D; Pigac, B; Hanzevacki, M; Marovic, A; Rucman, R; Petek, M; Zoricic, I; Ziger, T; Aralica, G; Konjevoda, P; Prkacin, I; Gjurasin, M; Miklic, P; Artukovic, B; Tisljar, M; Bratulic, M; Mise, S; Rotkvic, I · Animal Study

RPEP-00562 · 1999

BPC-157 Uniquely Protects Against Both External and Internal Stomach Irritants

BPC-157 maintained cytoprotective activity even when prostaglandin synthesis was blocked by indomethacin, unlike standard anti-ulcer agents, indicating prostaglandin-independent protective mechanisms for adaptive cytoprotection against endogenous irritants.

Sikirić, P; Seiwerth, S; Desković, S; Grabarević, Z; Marović, A; Rucman, R; Petek, M; Konjevoda, P; Jadrijević, S; Sosa, T; Perović, D; Aralica, G; Turković, B · Animal Study

RPEP-00563 · 1999

The Complete Landscape of Growth Hormone Releasing Compounds and Their Receptors

Structurally diverse GH secretagogues (peptides and non-peptides) all converge on the GHS receptor, whose cloning predicted the existence of a natural ligand — later identified as ghrelin — with widespread physiological roles beyond GH release.

Smith, R G; Palyha, O C; Feighner, S D; Tan, C P; McKee, K K; Hreniuk, D L; Yang, L; Morriello, G; Nargund, R; Patchett, A A; Howard, A D · Review

RPEP-00564 · 1999

MK-677 Raises Leptin But Doesn't Reduce Body Fat in Obese Men

MK-677 increased serum leptin levels independent of body fat changes, increased testosterone, and had no effect on thyroid hormones in obese males, revealing metabolic effects dissociated from fat mass changes.

Svensson, J; Carlsson, B; Carlsson, L M; Jansson, J O; Bengtsson, B A · RCT

RPEP-00565 · 1999

MK-677 Improves Cholesterol Profile in Obese Men But Raises Some Lipids Too

MK-677 produced mixed lipoprotein effects in obese males: beneficial increases in HDL and decreases in Lp(a), but also unfavorable increases in total cholesterol, LDL, and triglycerides over 8 weeks.

Svensson, J; Jansson, J O; Ottosson, M; Johannsson, G; Taskinen, M R; Wiklund, O; Bengtsson, B A · RCT

RPEP-00569 · 1999

Why ICU Patients Waste Muscle and How GH Peptides Could Fix It

Critical illness causes biphasic GH axis disruption; GH secretagogues + TRH restore physiological pulsatile GH secretion more safely than direct GH replacement, which increased mortality in a large clinical trial.

Van den Berghe, G · Review

RPEP-00570 · 1999

GHRP-2 Synchronizes Three Different Hormone Pulses in Critically Ill Patients

Continuous GHRP-2 infusion synchronized the pulsatile release of GH, TSH, and prolactin in critically ill patients, revealing a common hypothalamic regulatory mechanism that can be pharmacologically reactivated.

Van den Berghe, G; Wouters, P; Bowers, C Y; de Zegher, F; Bouillon, R; Veldhuis, J D · Clinical Trial

RPEP-00571 · 1999

The Heart and Blood Vessels Produce More Adrenomedullin During Sepsis

Adrenomedullin was locally upregulated in cardiac and aortic endothelial and smooth muscle cells during both early (hyperdynamic) and late (hypodynamic) sepsis stages, establishing cardiovascular tissue as a primary source.

Zhou, M; Chaudry, I H; Wang, P · Animal Study