RPEP-00341 · 1995SQ 28603 potentiated both ANP effects in monkeys (increased plasma ANP, sodium excretion) and BNP effects in hypertensive rats (blood pressure lowering, renal responses).
Seymour, A A; Abboa-Offei, B E; Smith, P L; Mathers, P D; Asaad, M M; Rogers, W L · Animal Study
RPEP-00342 · 1995N- or C-terminus modified dynorphin and beta-endorphin selectively blocked excitatory opioid receptor functions, dramatically enhancing the pain-relieving effects of opioid agonists.
Shen, K F; Crain, S M · In Vitro
RPEP-00344 · 1995DSIP administration produced marked changes in substance P, beta-endorphin, and corticosterone levels in both the hypothalamus and blood plasma. These changes persisted at both 1 hour and 24 hours after injection, indicating a prolonged cascade of molecular effects. The response pattern differed between Wistar rats and August rats — two strains with different baseline resistance to emotional stress. DSIP stimulated stress-resistance mechanisms more strongly in Wistar rats than in August rats, which are already more stress-resistant.
Sudakov, K V; Coghlan, J P; Kotov, A V; Salieva, R M; Polyntsev YuV; Koplik, E V ·
RPEP-00345 · 1995Beta-endorphin in the MPOA dose-dependently impaired male rat sexual behavior, prevented by naloxone, while other opioid peptides were less effective at equivalent doses.
van Furth, W R; van Emst, M G; van Ree, J M · Animal Study
RPEP-00346 · 1995Phorbol ester induced a concentration- and time-dependent increase in prodynorphin mRNA in cardiac myocytes, peaking at 4 hours and mediated through protein kinase C.
Ventura, C; Pintus, G; Vaona, I; Bennardini, F; Pinna, G; Tadolini, B · In Vitro
RPEP-00348 · 1995IGF-1 had a half-life of only 2 minutes in the duodenum and ileum, but casein protein significantly protected it from degradation in the gut.
Xian, C J; Shoubridge, C A; Read, L C · Animal Study
RPEP-00349 · 1995Fulminant hepatic failure significantly altered Met-enkephalin, Leu-enkephalin, dynorphin A, and beta-endorphin levels in multiple brain regions and plasma.
Yurdaydin, C; Li, Y; Ha, J H; Jones, E A; Rothman, R; Basile, A S · Animal Study
RPEP-00350 · 1995Opioid peptide levels in respiratory brainstem regions change significantly between young and older piglets, and prenatal cocaine exposure disrupts this developmental pattern.
Zhang, C; Moss, I R · Animal Study
RPEP-00351 · 1995Dynorphin peptides activate a cloned orphan receptor with high sequence homology to opioid receptors, functioning as its endogenous ligands via G protein-coupled potassium channel activation.
Zhang, S; Yu, L · In Vitro
RPEP-00352 · 1996GHRP-2 was considerably more potent than GHRP-6 at stimulating GH release through PKC-dependent pathways, and both caused crosstalk with the cAMP pathway in gsp oncogene-expressing tumors.
Adams, E F; Lei, T; Buchfelder, M; Bowers, C Y; Fahlbusch, R · In Vitro
RPEP-00353 · 1996GHRPs stimulate growth hormone release through a receptor distinct from GHRH, acting at both the pituitary and hypothalamic level, with consistent effects demonstrated across species and administration routes.
Argente, J; García-Segura, L M; Pozo, J; Chowen, J A · Review
RPEP-00354 · 1996Three CRF receptor subtypes (CRF1, CRF2alpha, CRF2beta) and a CRF-binding protein coordinate stress responses, and newly developed non-peptide CRF antagonists show therapeutic promise.
Behan, D P; Grigoriadis, D E; Lovenberg, T; Chalmers, D; Heinrichs, S; Liaw, C; De Souza, E B · Review
RPEP-00355 · 1996Endogenous opioid peptides in cerebral perivascular nerves and CSF actively regulate cerebral blood flow through opiate receptors, with concentrations changing in response to perfusion pressure and oxygen tension.
Benyó, Z; Wahl, M · Review
RPEP-00356 · 1996Multiple gastrointestinal peptide hormone levels were significantly altered during acute hepatic cytonecrosis and returned toward normal during liver regeneration.
Budillon, G; Cuomo, R; Taccone, W; Panico, G; Pumpo, R; Iaquinto, G; Manzillo, G · Cross Sectional
RPEP-00357 · 1996Daily oral MK-677 significantly stimulated the GH-IGF-1 axis in healthy elderly adults aged 64-81, raising levels toward those seen in younger individuals.
Chapman, I M; Bach, M A; Van Cauter, E; Farmer, M; Krupa, D; Taylor, A M; Schilling, L M; Cole, K Y; Skiles, E H; Pezzoli, S S; Hartman, M L; Veldhuis, J D; Gormley, G J; Thorner, M O · RCT
RPEP-00358 · 1996Bedtime MK-677 at 25 mg for 7 days significantly increased 24-hour GH profiles and IGF-1 in young men without altering adrenocortical function.
Copinschi, G; Van Onderbergen, A; L'Hermite-Balériaux, M; Mendel, C M; Caufriez, A; Leproult, R; Bolognese, J A; De Smet, M; Thorner, M O; Van Cauter, E · RCT
RPEP-00360 · 1996Cecropin B was the most potent antimicrobial peptide against B. pertussis, with cecropins generally outperforming magainins, defensins, and protamine.
Fernandez, R C; Weiss, A A · In Vitro
RPEP-00361 · 1996ANP, BNP, and cGMP were compared as screening markers for asymptomatic and symptomatic left ventricular dysfunction, with potential utility for early detection.
Friedl, W; Mair, J; Thomas, S; Pichler, M; Puschendorf, B · Cross Sectional
RPEP-00363 · 1996Antimicrobial peptide effectiveness against Brucella abortus depended significantly on bacterial surface structure, with rough mutants showing different susceptibility patterns than smooth strains.
Halling, S M · In Vitro
RPEP-00364 · 1996Plasma adrenomedullin concentrations were extremely elevated in septic ICU patients compared to healthy controls, correlating with disease severity.
Hirata, Y; Mitaka, C; Sato, K; Nagura, T; Tsunoda, Y; Amaha, K; Marumo, F · Cross Sectional
RPEP-00366 · 1996Conditioned enhancement of NK cell activity depends on mu-opioid receptor activation, with beta-endorphin and met-enkephalin as the key mediating peptides.
Hsueh, C M; Chen, S F; Huang, H J; Ghanta, V K; Hiramoto, R N · Animal Study
RPEP-00367 · 1996Chronic intracerebroventricular beta-endorphin infusion significantly enhanced in vivo NK cell cytotoxicity and altered splenic and peripheral blood lymphocyte phenotypes.
Jonsdottir, I H; Johansson, C; Asea, A; Hellstrand, K; Thorén, P; Hoffmann, P · Animal Study
RPEP-00368 · 1996KP-102 induces c-fos expression specifically in the arcuate nucleus, and this occurs even in hypophysectomized rats, confirming a direct hypothalamic site of action.
Kamegai, J; Hasegawa, O; Minami, S; Sugihara, H; Wakabayashi, I · Animal Study
RPEP-00370 · 1996Hexarelin maintained GH-releasing efficacy with repeated administration, and hexarelin plus GHRH produced a synergistic GH response exceeding individual effects.
Massoud, A F; Hindmarsh, P C; Matthews, D R; Brook, C G · RCT
RPEP-00372 · 1996NPY mediates analgesia and hyperalgesia through distinct receptor subtypes, alongside established roles in blood pressure regulation and anxiety modulation.
Munglani, R; Hudspith, M J; Hunt, S P · Review
RPEP-00373 · 1996Orphanin FQ/nociceptin suppressed dopamine release in the nucleus accumbens, acting opposite to classical opioids which typically increase dopamine in this reward-related region.
Murphy, N P; Ly, H T; Maidment, N T · Animal Study
RPEP-00374 · 1996Mu, delta, and kappa opioid receptors in cardiac sarcolemma activate pertussis toxin-sensitive G proteins and inhibit adenylyl cyclase, confirming a complete opioid signaling pathway in the heart.
Niroomand, F; Mura, R A; Piacentini, L; Kübler, W · In Vitro
RPEP-00375 · 1996Plasma BNP may increase proportionally more than ANP after acute myocardial infarction and chronic heart failure, potentially offering superior diagnostic and prognostic value.
Omland, T; Aakvaag, A; Bonarjee, V V; Caidahl, K; Lie, R T; Nilsen, D W; Sundsfjord, J A; Dickstein, K · Cohort
RPEP-00376 · 1996Pardaxin possesses high antibacterial activity, and engineered variants achieved potent bacterial killing while reducing harmful effects on mammalian cells.
Oren, Z; Shai, Y · In Vitro
RPEP-00377 · 1996Endogenous opioid peptides contribute to post-tetanic inhibition of gut muscle contractions, and peptidase inhibitors enhance this effect by protecting naturally released peptides from degradation.
Ozaki, M; Masuda, Y; Yamamoto, H · In Vitro
RPEP-00379 · 1996The GH secretagogue receptor was solubilized as a ~255 kDa receptor-ligand-G-protein complex from porcine pituitary, confirming it is distinct from the GHRH receptor.
Pomés, A; Pong, S S; Schaeffer, J M · In Vitro
RPEP-00380 · 1996A specific high-affinity G-protein-linked receptor for GH secretagogues was identified, operating through a distinct signaling pathway from GHRH.
Pong, S S; Chaung, L Y; Dean, D C; Nargund, R P; Patchett, A A; Smith, R G · In Vitro
RPEP-00381 · 1996Combination thymosin alpha-1 (1 mg twice weekly) and lymphoblastoid interferon was tested as a strategy to improve sustained response rates in chronic hepatitis C over interferon monotherapy.
Rasi, G; DiVirgilio, D; Mutchnick, M G; Colella, F; Sinibaldi-Vallebona, P; Pierimarchi, P; Valli, B; Garaci, E · RCT
RPEP-00383 · 1996BPC-157 provided strong gastroprotection against four distinct injury types (stress, ethanol, NSAID, capsaicin neurotoxicity), suggesting a broad protective mechanism involving sensory nerve pathways.
Sikirić, P; Seiwerth, S; Grabarević, Z; Rucman, R; Petek, M; Jagić, V; Turković, B; Rotkvić, I; Mise, S; Zoricić, I; Gjurasin, M; Konjevoda, P; Separović, J; Ljubanović, D; Artuković, B; Bratulić, M; Tisljar, M; Jurina, L; Buljat, G; Miklić, P; Marović, A · Animal Study
RPEP-00384 · 1996BPC-157 demonstrated both prophylactic and therapeutic effects in bile duct ligation-induced pancreatitis, also improving concomitant gastric and duodenal lesions.
Sikirić, P; Seiwerth, S; Grabarević, Z; Rucman, R; Petek, M; Jagić, V; Turković, B; Rotkvić, I; Mise, S; Zoricić, I; Jurina, L; Konjevoda, P; Hanzevacki, M; Ljubanović, D; Separović, J; Gjurasin, M; Bratulić, M; Artuković, B; Jelovac, N; Buljat, G · Animal Study
RPEP-00385 · 1996Proenkephalin-derived peptides increase hippocampal excitability via mu/delta receptors, while prodynorphin-derived peptides decrease it via kappa receptors, providing opposing regulation of memory circuits.
Simmons, M L; Chavkin, C · Review
RPEP-00386 · 1996GH secretagogues act through a novel receptor at dual sites (hypothalamus and pituitary) to amplify natural pulsatile GH release rather than creating continuous artificial elevation.
Smith, R G; Pong, S S; Hickey, G; Jacks, T; Cheng, K; Leonard, R; Cohen, C J; Arena, J P; Chang, C H; Drisko, J; Wyvratt, M; Fisher, M; Nargund, R; Patchett, A · Review
RPEP-00388 · 1996Approximately 40% of cardiac ganglion cells contained dynorphin A immunoreactivity, and opioid peptides were found in parasympathetic, sympathetic, and sensory cardiac nerves.
Steele, P A; Aromataris, E C; Riederer, B M · Animal Study
RPEP-00389 · 1996Peptidase inhibitors significantly prolonged the antinociceptive effect of intrathecally administered dynorphin A (0.5-2 nmol) and dynorphin B (2-8 nmol) in the formalin test.
Tan-No, K; Taira, A; Sakurada, T; Inoue, M; Sakurada, S; Tadano, T; Sato, T; Sakurada, C; Nylander, I; Silberring, J; Terenius, L; Kisara, K · Animal Study
RPEP-00391 · 1996GHRP-2 maintained GH-releasing efficacy in critically ill patients despite blunted responses to GHRH, suggesting a preserved alternative pathway for GH stimulation.
Van den Berghe, G; de Zegher, F; Bowers, C Y; Wouters, P; Muller, P; Soetens, F; Vlasselaers, D; Schetz, M; Verwaest, C; Lauwers, P; Bouillon, R · RCT
RPEP-00392 · 1996NEP inhibition with thiorphan significantly potentiated the blood pressure-lowering, hormonal, and renal effects of all three natriuretic peptides (ANP, BNP, CNP) in hypertensive transgenic rats.
Wegner, M; Ganten, D; Stasch, J P · Animal Study
RPEP-00393 · 1996NEP activity is increased in volume-overload heart failure, potentially accelerating the breakdown of protective natriuretic peptides even as the heart produces more of them.
Wegner, M; Hirth-Dietrich, C; Stasch, J P · Animal Study
RPEP-00394 · 1996Ad libitum access to a high-fat/sucrose diet significantly increased hypothalamic dynorphin peptide and mRNA levels compared to standard diet, suggesting opioid peptide-mediated overeating.
Welch, C C; Kim, E M; Grace, M K; Billington, C J; Levine, A S · Animal Study
RPEP-00395 · 1996GHRP-2 increased intracellular cAMP (like GHRH) while GHRP-6 released GH without raising cAMP, revealing partially different mechanisms despite similar GH-releasing outcomes.
Wu, D; Chen, C; Zhang, J; Bowers, C Y; Clarke, I J · In Vitro
RPEP-00396 · 1996BNP was superior to both C-terminal ANP and N-terminal ANP for detecting left ventricular systolic dysfunction, diastolic dysfunction, and ventricular hypertrophy.
Yamamoto, K; Burnett, J C; Jougasaki, M; Nishimura, R A; Bailey, K R; Saito, Y; Nakao, K; Redfield, M M · Cross Sectional
RPEP-00397 · 1997GHRP-2 and hexarelin both showed potent GH-releasing activity with slight stimulatory effects on prolactin, ACTH, and cortisol; their GH-releasing activities were directly compared for the first time.
Arvat, E; di Vito, L; Maccagno, B; Broglio, F; Boghen, M F; Deghenghi, R; Camanni, F; Ghigo, E · RCT
RPEP-00398 · 1997GHRP-2 stimulation revealed significant residual GH secretory potential in children classified as GH-deficient, with peak responses varying by growth disorder type.
Bercu, B B; Walker, R F · Clinical Trial
RPEP-00399 · 1997Antimicrobial peptide effectiveness against mollicutes varied dramatically by species, with animal defense peptides being less potent than venom and bacterial peptides. Multiple cellular effects preceded killing.
Béven, L; Wróblewski, H · In Vitro
RPEP-00400 · 1997Oral MK-677 stimulated GH and IGF-I in selected severely GH-deficient adults, with responses dependent on residual pituitary secretory capacity.
Chapman, I M; Pescovitz, O H; Murphy, G; Treep, T; Cerchio, K A; Krupa, D; Gertz, B; Polvino, W J; Skiles, E H; Pezzoli, S S; Thorner, M O · RCT
RPEP-00401 · 1997GHRP-2 and GHRP-6 each synergize with GRF/GHRH but combining both GHRPs at maximal doses adds no further GH release, confirming shared receptor competition.
Cheng, J; Wu, T J; Butler, B; Cheng, K · In Vitro