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Chemoreceptor trigger zone

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385:, physical injury, or over-excitation resulting in neuron death. Once the damage has occurred, the effects can cause the emetic response to disappear, or cause the emetic response to heighten, in some cases causing intractable vomiting that leave patients in severe distress. In cases such as these, if the damage is severe enough, little can be done to inhibit an intractable vomiting response because the chemoreceptors in the CTZ are physically damaged or hindered in some way. Recently, it has been discovered that physical changes in the area postrema and CTZ do cause or inhibit emesis. Specifically, compression of blood vessels which are physically located near in or around the CTZ, and that result in physical compression of the area postrema as a whole, have been found to be the cause of chronic medically intractable emesis and weight loss. Surgical microvascular decompression resulted in postoperative and long-term resolution of emesis. 397:) to bind to their respective receptors located in the CTZ. The antiemetic medications can block the binding site on a chemoreceptor in the CTZ, so that the emetic agent cannot bind to it to cause its emetic effects. Another way that antiemetic medications can work is by binding to a chemoreceptor in the CTZ, but instead of initiate vomiting, the medication can cause the receptors to send signals to the other parts of the vomiting center that inhibit emesis. Also, some anti-emetic medications work by lowering the amount of dopamine levels in the brain, which in turn effects how much dopamine comes in contact with dopamine receptors in the CTZ. Other antiemetic medications work similarly by lowering a different substance in the brain that is known to interact with chemoreceptors in the CTZ that cause emesis. 230:(NTS). The relaying happens by the initiation of an action potential, which is caused by the chemoreceptor causing a change in electric potential in the neuron it is embedded in, which then subsequently causes an action potential. This happens constantly, so the chemoreceptors in the CTZ are continually sending information about how much emetic agents are in the blood, even when emesis is not signaled for. The NTS is organized into subnuclei that direct many different functions relating to swallowing, gastric sensation, laryngeal and pharyngeal sensation, 226:. The activation of these opioid receptors in the CTZ are especially important for patients who take opioid based pain medications on a regular basis. However, opioids do not play a role in communication to the vomiting center of the brain, they only induce communication. Dopamine and serotonin have been found to play the biggest role in communication from the CTZ to the remainder of the vomiting center, as well as histamine. Chemoreceptors in the CTZ relay information about the presence of emetic agents in the blood to the adjacent 123:, or inner brain, and nothing more. This part of the brain is responsible for basic survival instincts and reactions, for example to make an organism turn its head and look where an auditory stimulus was heard. The brainstem is where the medulla is located, and therefore also the area postrema and the CTZ. Then later lifeforms developed another segment of the brain, which includes the 148:. This means that large polar molecules, such as emetic toxins, can diffuse through to and reach the CTZ quite easily. This is because the medulla oblongata is located in the area of the brain, the most inferior portion, which does not have a robust and highly developed blood-brain barrier. Without this barrier, emetic drugs and toxins are free to interact with a 373:, and higher order centers located in the cortex. The vomiting center is not a discrete or specific place in the brain, but rather an area consisting of many nuclei, axons, and receptors that together cause the physical changes necessary to induce vomiting. Also, emesis can occur by direct neural stimulation of the vomiting center. 197:
to initiate vomiting. This is because the CTZ sends the "vomit" command through action potentials, and these specific action potentials that trigger emesis are only produced when a certain amount of opioids bind to a certain amount of opioid receptors in the CTZ. Neurons in the CTZ, and area postrema
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is the most recent development. This area of the brain is responsible for critical thinking and reasoning, and is actively involved in decision making. It has been discovered that a major cause of increased intelligence in species including humans is the increase in cortical neurons in the brain. The
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Oftentimes, doctors will "pre-treat" patients who might exhibit emetic responses due to drugs they prescribe them. Usually pain relieving drugs such as opioids are co-prescribed with anti-emetic drugs to stop the emetic response due to the pain reliever before it can even mediate its effects on the
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receptors. It has been seen that intraventricular administration of histamine in dogs causes an emetic response. This shows that histamine plays a significant role in signaling for emetic action in the CTZ. Some classes of molecules have been shown to inhibit the emetic response due to histamine,
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receptors. It has been discovered that the cholinergic neurons are actually nicotinic. These receptors are meant to monitor the amount of associated neurotransmitter of these receptors in the blood. For instance, the CTZ has opioid receptors that monitor the level of opioids in the blood, and when
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Most of the neurons located in the CTZ express hyperpolarization-activated cation channels (H-channels). Since the neurons in the CTZ convey information relating to emesis to the other parts of the vomiting center, it was thought that these H-channels might play a role in nausea and the emetic
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The receptors on the surface of the neuron are chemoreceptors that are activated from direct contact of emetic substances in the blood, whereas the receptors that are deeper down on the dendrites are receptors that are activated in response to the activated chemoreceptors on the surface.
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is a major cause of emesis, and often can cause severe and frequent emetic responses. This is because chemotherapy agents circulating in the blood activate the CTZ in such a way as to cause emesis. Patients receiving chemotherapy are often prescribed antiemetic medications.
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This integrates the emetic response. This is the area in which "a final decision is made" about whether to evoke an emetic response. This decision is based heavily on the information which the CTZ relays to the rest of the vomiting center, but also the chemoreceptors in the
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Mori, F; PĂ©rez-Torres, S; De Caro, R; Porzionato, A; Macchi, V; Beleta, J; GavaldĂ , A; Palacios, JM; Mengod, G (September 2010). "The human area postrema and other nuclei related to the emetic reflex express cAMP phosphodiesterases 4B and 4D".
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emetic response was selected for protective purposes, and serves as a safeguard against poisoning of the body. This response gets toxins and drugs out of the body by summoning control over motor neurons which stimulate muscles in the chest and
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Root, AR; Nucci, NV; Sanford, JD; Rubin, BS; Trudeau, VL; Sower, SA (2005). "In situ characterization of gonadotropin- releasing hormone-I, -III, and glutamic acid decarboxylase expression in the brain of the sea lamprey, Petromyzon marinus".
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Mortazavi, Martin M.; Tubbs, R. Shane; Harmon, Daniel; Oakes, W. Jerry (December 2010). "Chronic emesis due to compression of the area postrema by the posterior inferior cerebellar artery: resolution following microvascular decompression".
238:(CPG). This CPG actually coordinates the sequences of physical movements during emesis. The main neurotransmitters involved in communication between the CTZ and remaining vomiting center are serotonin, dopamine, histamine, and 167:
The CTZ has many different types of receptors, which are specific to different types of toxins or drugs that might be present in the bloodstream and thus that can affect the CTZ. Types of CTZ receptors include
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response. Recently, evidence of this notion that H-channels in CTZ neurons play a role in emesis has come to light. It has been found that ZD7288, which is a H-channel inhibitor, inhibited the acquisition of
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and blood vessels associated with the CTZ neurons. PDE4 mRNAs are transcribed more in the area postrema and the CTZ than anywhere else in the brainstem. The PDE4 degrades the phosphodiester bonds in the
127:. This area of the brain is responsible for producing emotion and emotional responses to external stimuli, and also is significantly involved in memory and reward systems. Evolutionarily, the 335:(cAMP), which is one of the ways the brain relays information. By modifying cAMP signaling in the CTZ, it is thought that this could mediate the emetic effects of PDE4 inhibitors in the CTZ. 356:
expression in the area postrema where the CTZ is located. This suggests that the neurons that express H-channels in the CTZ and area postrema are involved in nausea and the emetic response.
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Shinpo, K; Hirai, Y; Maezawa, H; Totsuka, Y; Funahashi, M (20 August 2012). "The role of area postrema neurons expressing H-channels in the induction mechanism of nausea and vomiting".
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Antiemetic medications often target the CTZ to completely inhibit or greatly reduce vomiting. Most of these work by not allowing certain blood-borne drugs (usually pain killers or
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Essentials of neurosurgical anesthesia & critical care : strategies for prevention, early detection, and successful management of perioperative complications
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Hori, N. et al. (2000). Brainstem slice studies of receptor activation in the mouse area postrema. Society for Neuroscience Abstracts. 26(1-2) Abstract No.-716.13.
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CTZ. This way, the patient does not have to worry about the doctors prescription to treat their pain causing them to be in severe discomfort via vomiting.
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The vomiting center of the brain refers to the groups of loosely organized neurons in the medulla that include the CTZ within the area postrema and the
314:, cause emesis as one of their side effects. It has been found that these PDE4 isoforms are expressed in the CTZ and in the brainstem in general. The 666:"Nausea and Vomiting Side Effects with Opioid Analgesics during Treatment of Chronic Pain: Mechanisms, Implications, and Management Options" 160:. These neurotransmitters implement their effects on the CTZ receptors by binding to them which sets off a chain of events that produces an 457: 198:
in general, actually have two types of receptors: those at the surface of the neuron and those that are located deeper down in the
218:. One of the ways the chemoreceptor trigger zone implements its effects on the vomiting center is by activation of the opioid 332: 193:
the amount of opioids in the blood reaches a certain level, the opioid receptors in the CTZ will signal to the rest of the
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Encarnacion, H. J. et al. (2009). Vomiting. Compendium-Continuing Education for Veterinarians. 31(3): 122-+.
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products from genes that code for these PDE4 isoforms are plentiful in the CTZ, and not only located in CTZ
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Since the CTZ is located in the area postrema, a sensory circumventricular organ, it does not have a
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The CTZ communicates with the other parts of the vomiting center through neurons that contain
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is not as developed here; therefore, drugs such as dopamine which cannot normally enter the
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because they interact with different types of molecules which are usually referred to as
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Hornby, Pamela J. (December 2001). "Central neurocircuitry associated with emesis".
577: 818: 621: 427: 414: 231: 219: 876: 152:, or multiple receptors located in the CTZ. These receptors in the CTZ are called 349: 323: 247: 181: 84: 973: 528: 511: 394: 291: 287: 243: 234:
function, and respiration. The NTS directs signals about these functions to a
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the oldest part of the central nervous system. Early lifeforms developed a
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Miller AD, Leslie RA (Dec 1994). "The area postrema and vomiting".
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Area of the medulla oblongata that receives inputs for vomiting
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Continuing Education in Anaesthesia, Critical Care & Pain
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present, which may be involved in the mechanism by which
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editors, Ansgar M. Brambrink, Jeffrey R. Kirsch (2012).
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Antiemetic drugs coupled with pain relieving medications
369:, the information sent to the vomiting center by the 63:. It is also part of the vomiting center itself. The 452:(2012 ed.). New York: Springer. p. 716. 505: 503: 664:Porreca, Frank; Ossipov, Michael H. (May 2009). 43:, and communicates with other structures in the 115:The CTZ is in the medulla oblongata, which is 8: 915: 913: 911: 741: 739: 981: 858: 856: 854: 826: 771: 746:Bhargava, KP; Dixit, KS (November 1968). 681: 659: 657: 655: 653: 651: 649: 647: 645: 527: 510:Pierre, S.; Whelan, R. (11 August 2012). 492:CS1 maint: multiple names: authors list ( 962:Journal of the Royal Society of Medicine 703: 701: 543: 541: 539: 438: 799: 797: 795: 793: 791: 635: 633: 631: 482: 472: 7: 136:to expel contents from the stomach. 923:Journal of Neurosurgery: Pediatrics 512:"Nausea and vomiting after surgery" 764:10.1111/j.1476-5381.1968.tb08479.x 14: 91:(5-HT3 receptor). There are also 807:Journal of Chemical Neuroanatomy 710:The American Journal of Medicine 683:10.1111/j.1526-4637.2009.00583.x 360:The vomiting center of the brain 51:. The CTZ is located within the 752:British Journal of Pharmacology 550:Frontiers in Neuroendocrinology 381:Damage to the CTZ can come via 306:Recent studies have found that 99:cause nausea and vomiting. The 55:, which is on the floor of the 819:10.1016/j.jchemneu.2010.03.004 333:cyclic adenosine monophosphate 1: 956:Edwards, CM (November 1988). 877:10.1016/j.physbeh.2012.06.002 722:10.1016/S0002-9343(01)00849-X 594:Brain, Behavior and Evolution 310:4 (PDE4) inhibitors, such as 107:may still stimulate the CTZ. 67:implicated in the control of 1027: 974:10.1177/014107688808101115 348:(CTA) in rats and reduced 346:conditioned taste aversion 31:that receives inputs from 21:chemoreceptor trigger zone 865:Physiology & Behavior 236:central pattern generator 228:nucleus tractus solitarii 216:nucleus tractus solitarii 111:Evolutionary significance 935:10.3171/2010.9.PEDS10291 529:10.1093/bjaceaccp/mks046 562:10.1006/frne.1994.1012 389:Antiemetic medications 59:and is outside of the 87:(NK-1 receptor), and 71:and vomiting include 27:) is an area of the 146:blood–brain barrier 101:blood–brain barrier 61:blood–brain barrier 485:has generic name ( 302:Phosphodiesterases 240:endogenous opioids 134:thoracic diaphragm 606:10.1159/000081354 377:Damage to the CTZ 371:vestibular system 308:phosphodiesterase 158:neurotransmitters 65:neurotransmitters 29:medulla oblongata 1018: 996: 995: 985: 953: 947: 946: 917: 906: 903: 897: 896: 860: 849: 848: 830: 801: 786: 785: 775: 743: 734: 733: 705: 696: 695: 685: 661: 640: 637: 626: 625: 588: 582: 581: 545: 534: 533: 531: 507: 498: 497: 490: 484: 480: 478: 470: 468: 466: 443: 329:second messenger 162:action potential 117:phylogenetically 93:opioid receptors 57:fourth ventricle 1026: 1025: 1021: 1020: 1019: 1017: 1016: 1015: 1011:Neurophysiology 1001: 1000: 999: 955: 954: 950: 919: 918: 909: 904: 900: 862: 861: 852: 803: 802: 789: 745: 744: 737: 707: 706: 699: 663: 662: 643: 638: 629: 590: 589: 585: 547: 546: 537: 509: 508: 501: 491: 481: 471: 464: 462: 460: 445: 444: 440: 436: 424: 412: 403: 391: 379: 362: 341: 304: 283: 276: 269: 262: 224:delta receptors 212: 195:vomiting center 142: 129:cerebral cortex 113: 83:(H1 receptor), 45:vomiting center 17: 12: 11: 5: 1024: 1022: 1014: 1013: 1003: 1002: 998: 997: 968:(11): 658–62. 948: 929:(6): 583–585. 907: 898: 850: 787: 735: 716:(8): 106–112. 697: 676:(4): 654–662. 641: 627: 583: 535: 499: 459:978-0387095615 458: 437: 435: 432: 431: 430: 423: 420: 411: 408: 402: 399: 390: 387: 378: 375: 361: 358: 340: 337: 322:, but also in 303: 300: 286:these include 281: 274: 267: 260: 242:which include 211: 208: 154:chemoreceptors 141: 140:Chemoreception 138: 112: 109: 15: 13: 10: 9: 6: 4: 3: 2: 1023: 1012: 1009: 1008: 1006: 993: 989: 984: 979: 975: 971: 967: 963: 959: 952: 949: 944: 940: 936: 932: 928: 924: 916: 914: 912: 908: 902: 899: 894: 890: 886: 882: 878: 874: 871:(1): 98–103. 870: 866: 859: 857: 855: 851: 846: 842: 838: 834: 829: 824: 820: 816: 812: 808: 800: 798: 796: 794: 792: 788: 783: 779: 774: 769: 765: 761: 758:(3): 508–13. 757: 753: 749: 742: 740: 736: 731: 727: 723: 719: 715: 711: 704: 702: 698: 693: 689: 684: 679: 675: 671: 670:Pain Medicine 667: 660: 658: 656: 654: 652: 650: 648: 646: 642: 636: 634: 632: 628: 623: 619: 615: 611: 607: 603: 599: 595: 587: 584: 579: 575: 571: 567: 563: 559: 556:(4): 301–20. 555: 551: 544: 542: 540: 536: 530: 525: 521: 517: 513: 506: 504: 500: 495: 488: 476: 461: 455: 451: 450: 442: 439: 433: 429: 426: 425: 421: 419: 416: 409: 407: 400: 398: 396: 388: 386: 384: 376: 374: 372: 368: 359: 357: 355: 351: 347: 338: 336: 334: 330: 325: 321: 317: 313: 309: 301: 299: 297: 293: 289: 284: 277: 270: 263: 255: 253: 249: 245: 241: 237: 233: 229: 225: 221: 217: 210:Communication 209: 207: 203: 201: 196: 191: 190:acetylcholine 187: 183: 179: 175: 171: 165: 163: 159: 155: 151: 147: 139: 137: 135: 130: 126: 125:limbic system 122: 118: 110: 108: 106: 102: 98: 94: 90: 86: 82: 78: 74: 73:acetylcholine 70: 66: 62: 58: 54: 53:area postrema 50: 46: 42: 38: 34: 30: 26: 22: 965: 961: 951: 926: 922: 901: 868: 864: 828:10261/147758 813:(1): 36–42. 810: 806: 755: 751: 713: 709: 673: 669: 600:(1): 60–70. 597: 593: 586: 553: 549: 522:(1): 28–32. 519: 515: 483:|last1= 463:. 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Index

medulla oblongata
blood
drugs
hormones
vomiting center
vomiting
area postrema
fourth ventricle
blood–brain barrier
neurotransmitters
nausea
acetylcholine
dopamine
histamine
substance P
serotonin
opioid receptors
opiates
blood–brain barrier
CNS
phylogenetically
brainstem
limbic system
cerebral cortex
thoracic diaphragm
blood–brain barrier
receptor
chemoreceptors
neurotransmitters
action potential

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