Research context
A peptide studied in reproductive neuroendocrinology and GnRH signalling.
Reproductive research
A peptide studied in reproductive neuroendocrinology and GnRH signalling.
A peptide studied in reproductive neuroendocrinology and GnRH signalling.
Evidence map
Evidence levels describe study design. They do not by themselves establish safety or effectiveness.
Maternal Kisspeptin-10 Treatment Partially Rescues Fetal and Postnatal Cardiac Programming Disrupted by Maternal Hypothyroidism.
Structural basis for Kisspeptin-10 selectivity toward KISS1R: computational insights.
Kisspeptin System: A Modulator of Neuroinflammation and Behaviour in Temporal Lobe Epileptic Rats.
Chronic subcutaneous kisspeptin-10 stimulates gonadotropin secretion for 12 days in healthy men.
The kisspeptin analog C6 elicits greater tachyphylaxis and transcriptional activation than kisspeptin-10 and -54.
Kisspeptin-10/basal LH ratio improves differentiation of central precocious puberty and premature thelarche.
Exogenous Kisspeptin-10 inhibits ovarian cancer progression through targeting the SP1-hTERT-ZEB1 regulatory axis.
Evaluation of Kisspeptin Glucose-Stimulated Insulin Secretion With Physiologic Mixed Meal Tolerance
Age-dependent Changes in the Responsiveness of Hypothalamic Pituitary Gonadal Axis in Men
Link Between the Sensitivity of Kisspeptin Signalling and Pubertal Onset in Boys.
Evaluation of Kisspeptin Stimulated Insulin Secretion With Hyperglycemic Clamp
KP-10 and Insulin Secretion in Men
Enzymatic Stability and Comparative Effects of Kisspeptin-14, Kisspeptin-13 and Kisspeptin-10 on Beta-Cell Function, Glucose Homeostasis and Appetite Regulation.
Enzymatic Stability and Comparative Effects of Kisspeptin-14, Kisspeptin-13 and Kisspeptin-10 on Beta-Cell Function, Glucose Homeostasis and Appetite Regulation.
Maternal Kisspeptin-10 Treatment Partially Rescues Fetal and Postnatal Cardiac Programming Disrupted by Maternal Hypothyroidism.
Kisspeptin-10 regulates glycosaminoglycan and decorin content in human cardiac fibroblast cultures.
Dynamic modulation of LH secretion by continuous kisspeptin infusion in healthy men.
The KISS1/KISS1R Axis in Human Placentation: Molecular Mechanisms and Implications for Foetal Growth Restriction and Pre-Eclampsia.
Relationship between kisspeptin-10, neurokinin B and dynorphin A in the course of normal and delayed puberty in ewes.
Role of kisspeptin on cell proliferation and steroidogenesis in luteal cells in vitro and in vivo.
Kisspeptin Restores Placental mTOR Signaling and Improves Glucose Homeostasis Mediators Disrupted by Maternal Hypothyroidism in Rats.
Fig. 1. Number of runs between arms in the elevated plus maze test. Intact — intact group of mice without any treatment; Sat. r. VB — intraperitoneal administration of 0.9% sodium chloride solution; Sat. r. IN — intranasal administration of 0.9% sodium chloride solution; Kisspeptin IN 0.1 — intranasal administration of kisspeptin-10 at a dosage of 0.1 μg; Kisspeptin IN 1 — intranasal administration of kisspeptin-10 at a dosage of 1 μg; Kisspeptin IN 10 — intranasal administration of kisspeptin-10 at a dosage of 10 μg; Kisspeptin VB 1 — intraperitoneal administration of kisspeptin-10 at a dosage of 1 μg; Kisspeptin VB 10 — intraperitoneal administration of kisspeptin-10 at a dosage of 10 μg; Kisspeptin VB 100 — intraperitoneal administration of kisspeptin-10 at a dosage of 100 μg. *p <0.05; **p <0.01 — differences between intact and experimental animals.
Fig. 1. Number of arm entries in the elevated plus maze. Intact, intact group of animals without intervention; NaCl IP, intraperitoneal administration of 0.9% sodium chloride solution; NaCl IN, intranasal administration of 0.9% sodium chloride solution; kisspeptin 0.1 IN, intranasal administration of kisspeptin-10 at a dose of 0.1 µg; kisspeptin 1 IN, intranasal administration of kisspeptin-10 at a dose of 1 µg; kisspeptin 10 IN, intranasal administration of kisspeptin-10 at a dose of 10 µg; kisspeptin 1 IP, intraperitoneal administration of kisspeptin-10 at a dose of 1 µg; kisspeptin 10 IP, intraperitoneal administration of kisspeptin-10 at a dose of 10 µg; kisspeptin 100 IP, intraperitoneal administration of kisspeptin-10 at a dose of 100 µg.*р < 0.05; **р < 0.01, differences between intact and experimental animals.
Fig. 1. Animal behavior in the sexual motivation test following intraperitoneal (i.p.) injection of 0.9% sodium chloride solution and kisspeptin-10: a, latency period; b, number of approaches to the female. 1, intact (intact group of animals without intervention); 2, i.p. kisspeptin 1 (intraperitoneal injection of kisspeptin-10 at a dose of 1 µg); 3, i.p. kisspeptin 10 (intraperitoneal injection of kisspeptin-10 at a dose of 10 µg); 4, i.p. kisspeptin 100 (intraperitoneal injection of kisspeptin-10 at a dose of 100 µg); 5, i.p. saline (intraperitoneal injection of 0.9% sodium chloride solution). Data are presented as M ± m. *p ≤ 0.05, difference between the kisspeptin-10 group and the intact group.
Are all kisspeptins equal? The effect of kisspeptin 10 and kisspeptin 54 on kisspeptin-mediated signalling
Cross-Linking Furan-Modified Kisspeptin-10 to the KISS Receptor
Kisspeptin-10 - ein potenzieller Inhibitor der Invasion humaner Endometriumkarzinomzellen
Fig. 2. Number of mounts per female. 1, means intact controls; 2, means restraint stress without drug introduction; 3, means restraint stress + kisspeptin-10 intranasally (single introduction); 4, means restraint stress + kisspeptin-10 intraperitoneally (single introduction); 5, means restraint stress + kisspeptin-10 intranasally (5-day introduction course); 6, means restraint stress + kisspeptin-10 intraperitoneally (5-day introduction course). ##p < 0.01 relative to animal group exposed to restraint stress; ***p < 0.001 relative to intact controls.
Fig. 1. Effect of intranasal and intraperitoneal administration of kisspeptin-10 on the level of gonadotropin-releasing hormone in the hypothalamus of animals with posttraumatic stress disorder induced by restraint stress or vital stress. Here and in Figs. 2 and 3: 1, intact control; 2, restraint stress; 3, restraint stress + kisspeptin-10 intranasal (5-day treatment course); 4, restraint stress + kisspeptin-10 intraperitoneal (5-day treatment course); 5, vital stress; 6, vital stress + kisspeptin-10 intranasal (5-day treatment course); 7, vital stress + kisspeptin-10 intraperitoneal (5-day treatment course). *p = 0.0468 vs. the intact control group; #p = 0.0246 vs. the restraint stress group; $p = 0.0002 vs. the vital stress group.
Rapid and harmonized analytical workflow for the determination of peptidic and non-peptidic doping agents in dried and liquid blood matrices.
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The goal of this study is to understand how exogenous kisspeptin affects metabolism by evaluating responses to an hyperglycemic clamp
This study utilizes infusions of kisspeptin in healthy women to isolate the impact of kisspeptin on beta-cell responsivity assessed by the mixed meal tolerance test.
Induction of insulin secretion by kisspeptin is observed in mouse, pig, rat, and human islets in vitro and in rats, mice and monkeys in vivo, but its mechanism is not fully clear. The present study was designed to...
The present study was designed to assess the responsiveness of the hypothalamic pituitary gonadal axis to kisspeptin administration with increasing age in men.
The specific objective of this study was to investigate the sensitivity of Kisspeptin receptor 1 (KISS1R) by determining the responsiveness of GnRH neuron to kisspeptin administration across the pubertal stages and adult group through measuring plasma LH (luteinizing...
Robert V, Lomet D, Dardente H, Aucagne V, Beltramo M
Netesa MA, Pyurveev SS, Lebedev AA, Bychkov ER, Skorb EV, Shityakov S, Shabanov PD
Shah H, Thomas A, Pandya P
Spratt JA, Tanday N, McGinn DM, Chukwu CD, Gault VA, Irwin N
Barbosa EM, Rodrigues NP, Santos BR, Dos Anjos Cordeiro JM, da Silva TQM, Oliveira CL, Santos LC, Cunha MCDSG, Serakides R, Silva JF
Jaldhi, Kumar S, Shanker OR, Banerjee J, Dixit AB, Maurya SK, Bakshi A
Yeung AC, Phylactou M, Koysombat K, Tsoutsouki J, Nyunt SW, Young M, Patel AH, Daniels E, Pierret ACS, Mills EG, Comninos AN, Abbara A, Dhillo WS
Banerjee AA, Bhanarkar SR, Kashikar S, Keshwani R, Walia S, Kavya DR, Bombe S, Pande S, Modi DN, Pathak BR, Joshi B, Tandon D, Patil A, Begum S, Mahale SD, Rao S, Surve SV
Mazzarino M, Colpaert T, Deventer K, Van Eenoo P
Spratt JA, Tanday N, McGinn DM, Chukwu CD, Gault VA, Irwin N · Metabolites
Radwańska P, Olkiewicz M, Piera L, Drobnik J · Pharmacological reports : PR
Santos BR, Dos Anjos Cordeiro JM, Santos LC, Oliveira CS, Alvarez MCPS, Rodrigues NP, Lopez-Tello J, Sferruzzi-Perri AN, Serakides R, Silva JF · Acta physiologica (Oxford, England)
Szysiak N, Kosior-Korzecka U, Greguła-Kania M, Patkowski K, Fila M, Junkuszew A · Journal of veterinary research
Barbosa EM, Rodrigues NP, Santos BR, Dos Anjos Cordeiro JM, da Silva TQM, Oliveira CL, Santos LC, Cunha MCDSG, Serakides R, Silva JF · Cardiovascular toxicology
Naveed A, Lippincott MF, Stamou M, Balasubramanian R, Bryant NK, Seminara SB · Hormones (Athens, Greece)
Gyokova E, Hristova-Atanasova E, Dimitrova K · International journal of molecular sciences
Chiang CM, Chiu HY, Chang CS, Chien YY, Jong DS, Wu LS, Chiu CH · Journal of the Chinese Medical Association : JCMA
Svaty Sachania, Naushin Nawar, Aaron Ghelut, Waljit Dhillo, Kim C Jonas · Bioscientifica
· ECO-Vector LLC (Publications)
· ECO-Vector LLC (Publications)
· ECO-Vector LLC (Publications)
· American Chemical Society (ACS)
Elena Schmidt · University Goettingen Repository
· ECO-Vector LLC (Publications)
· ECO-Vector LLC (Publications)
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