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Immune-selective anti-inflammatory derivative

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51:. Early work in this area demonstrated that the submandibular gland released a host of factors which regulate systemic inflammatory responses and modulate systemic immune and inflammatory reactions. Early work in identifying factors that played a role in the CST-SMG axis lead to the discovery of a seven 91:
Cellular Effects of feG: The cellular effects of the ImSAIDs are characterized in a number of publications. feG and related peptides are known to modulate leukocyte (white blood cells) activity by influencing cell surface receptors to inhibit excessive activation and tissue infiltration. One lead
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exposure. SGP-T, an isolate of the submandibular gland, demonstrated its immunoregulatory properties and potential role in modulating the cervical sympathetic trunk-submandibular gland (CST-SMG) axis, and subsequently was shown to play an important role in the control of inflammation.
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Dery, RE; Ulanova, M; Puttagunta, L; Stenton, GR; James, D; Merani, S; Mathison, R; Davison, J; Befus, AD (Dec 2004). "Frontline: Inhibition of allergen-induced pulmonary inflammation by the tripeptide feG: a mimetic of a neuro-endocrine pathway".
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nerves. This pathway or communication is referred to as the cervical sympathetic trunk-submandibular gland (CST-SMG) axis, a regulatory system that plays a role in the systemic control of inflammation.
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Bao, F; John, SM; Chen, Y; Mathison, RD; Weaver, LC (2006). "The tripeptide phenylalanine-(D) glutamate-(D) glycine modulates leukocyte infiltration and oxidative damage in rat injured spinal cord".
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repair. One of the neuroendocrine pathways, when activated, results in the release of immune regulating peptides from the submandibular gland upon neuronal stimulation from
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Mathison, R; Lo, P; Tan, D; Scott, B; Davison, JS (Dec 2001). "The tripeptide feG reduces endotoxin-provoked perturbation of intestinal motility and inflammation".
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Mathison, RD; Malkinson, T; Cooper, KE; Davison, JS (May 1997). "Submandibular glands: novel structures participating in thermoregulatory responses".
96:, and inhibit the binding of CD16b (FCyRIII) antibody to human neutrophils. One ImSAID, termed feG, has also been shown to decrease circulating 279:
Mathison, R; Davison, JS; Befus, AD (Nov 1994). "Neuroendocrine regulation of inflammation and tissue repair by submandibular gland factors".
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Mathison, RD; Davison, JS (Jun 2006). "The Tripeptide feG Regulates the Production of Intracellular Reactive Oxygen Species by Neutrophils".
58:, called the submandibular gland peptide-T. SGP-T was demonstrated to have biological activity and thermoregulatory properties related to 482: 43:
hormones or non steroidal anti-inflammatories. The ImSAIDs were discovered by scientists evaluating biological properties of the
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ImSAID, the tripeptide FEG (Phe-Glu-Gly) and its D-isomer feG are known to alter leukocyte adhesion involving actions on Ī±MĪ²2
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that have anti-inflammatory properties. ImSAIDs work by altering the activation and migration of
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The ImSAIDs represent a new category of anti-inflammatory and are unrelated to
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One SGP-T derivative is a three amino acid sequence shown to be a potent
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activity and reduced the expression of CD49d after antigen exposure,.
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form (feG), have become the foundation for the ImSAID category.
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Mathison, RD; Befus, AD; Davison, JS; Woodman, RC (Mar 2003).
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cells responsible for amplifying the inflammatory response.
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Dery RE, Mathison R, Davison J, Befus AD. "Inhibition of
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with systemic effects. This three amino acid peptide is
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systems communicate and interact to control and modulate
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It is now well accepted that the immune, nervous and
314:Mathison, RD; Christie, E; Davison, JS (May 2008). 316:"The tripeptide feG inhibits leukocyte adhesion" 17:Immune Selective Anti-Inflammatory Derivatives 8: 458:inflammation by C-terminal peptides of the 341: 331: 218: 208: 148: 104:accumulation, decrease intracellular 7: 170:10.1016/j.neuroscience.2006.02.061 14: 434:10.1046/j.1365-2982.2001.00294.x 67:Mechanisms or ImmunoPharmacology 1: 462:submandibular rat 1 (SMR-1). 293:10.1016/0167-5699(94)90209-7 466:2001 an-Mar;124(1-3):201-4. 499: 464:Int Arch Allergy Immunol. 19:(ImSAIDs) are a class of 483:Anti-inflammatory agents 422:Neurogastroenterol Motil 245:Can J Physiol Pharmacol 380:10.1002/eji.200425461 333:10.1186/1476-9255-5-6 210:10.1186/1471-2172-4-3 45:submandibular gland 118:anti-inflammatory 27:cells, which are 490: 467: 452: 446: 445: 417: 411: 410: 403:J Inflamm (Lond) 398: 392: 391: 362: 356: 355: 345: 335: 320:J Inflamm (Lond) 311: 305: 304: 276: 270: 269: 239: 233: 232: 222: 212: 188: 182: 181: 153: 135:(FEG) and its D- 498: 497: 493: 492: 491: 489: 488: 487: 473: 472: 471: 470: 453: 449: 419: 418: 414: 400: 399: 395: 374:(12): 3315ā€“25. 364: 363: 359: 313: 312: 308: 278: 277: 273: 258:10.1139/y97-077 241: 240: 236: 190: 189: 185: 155: 154: 150: 145: 114: 69: 37: 12: 11: 5: 496: 494: 486: 485: 475: 474: 469: 468: 447: 428:(6): 599ā€“603. 412: 393: 357: 306: 287:(11): 527ā€“32. 271: 234: 183: 164:(3): 1011ā€“22. 147: 146: 144: 141: 113: 110: 68: 65: 36: 33: 13: 10: 9: 6: 4: 3: 2: 495: 484: 481: 480: 478: 465: 461: 457: 451: 448: 443: 439: 435: 431: 427: 423: 416: 413: 408: 404: 397: 394: 389: 385: 381: 377: 373: 369: 368:Eur J Immunol 361: 358: 353: 349: 344: 339: 334: 329: 325: 321: 317: 310: 307: 302: 298: 294: 290: 286: 282: 281:Immunol Today 275: 272: 267: 263: 259: 255: 252:(5): 407ā€“13. 251: 247: 246: 238: 235: 230: 226: 221: 216: 211: 206: 202: 198: 194: 187: 184: 179: 175: 171: 167: 163: 159: 152: 149: 142: 140: 138: 134: 130: 126: 125:phenylalanine 122: 119: 112:Lead Compound 111: 109: 107: 103: 99: 95: 89: 86: 82: 78: 74: 66: 64: 61: 57: 54: 50: 46: 42: 34: 32: 30: 26: 22: 18: 463: 450: 425: 421: 415: 406: 402: 396: 371: 367: 360: 323: 319: 309: 284: 280: 274: 249: 243: 237: 200: 196: 186: 161: 158:Neuroscience 157: 151: 115: 90: 77:inflammation 70: 38: 25:inflammatory 16: 15: 197:BMC Immunol 85:sympathetic 460:prohormone 143:References 102:eosinophil 98:neutrophil 53:amino acid 129:glutamine 106:oxidative 73:endocrine 60:endotoxin 477:Category 456:allergic 442:11903921 388:15549777 352:18492254 229:12659660 178:16581192 137:isomeric 121:molecule 94:integrin 21:peptides 409:(1): 9. 343:2408570 301:7802923 266:9250374 133:glycine 56:peptide 41:steroid 35:History 440:  386:  350:  340:  299:  264:  227:  220:152650 217:  176:  81:tissue 49:saliva 29:immune 326:: 6. 203:: 3. 438:PMID 384:PMID 348:PMID 297:PMID 262:PMID 225:PMID 174:PMID 100:and 79:and 47:and 430:doi 376:doi 338:PMC 328:doi 289:doi 254:doi 215:PMC 205:doi 166:doi 162:140 479:: 436:. 426:13 424:. 405:. 382:. 372:34 370:. 346:. 336:. 322:. 318:. 295:. 285:15 283:. 260:. 250:75 248:. 223:. 213:. 199:. 195:. 172:. 160:. 444:. 432:: 407:3 390:. 378:: 354:. 330:: 324:5 303:. 291:: 268:. 256:: 231:. 207:: 201:4 180:. 168:: 131:- 127:-

Index

peptides
inflammatory
immune
steroid
submandibular gland
saliva
amino acid
peptide
endotoxin
endocrine
inflammation
tissue
sympathetic
integrin
neutrophil
eosinophil
oxidative
anti-inflammatory
molecule
phenylalanine
glutamine
glycine
isomeric
doi
10.1016/j.neuroscience.2006.02.061
PMID
16581192
"Modulation of neutrophil function by the tripeptide feG"
doi
10.1186/1471-2172-4-3

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