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																		 Opioid Peptides
 
																		 
																		
																	 
																		 
																		
																	 
																			
																					
	"Opioid Peptides" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, 
	MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, 
	which enables searching at various levels of specificity.
 
	
	
		
			
			
				The endogenous peptides with opiate-like activity. The three major classes currently recognized are the ENKEPHALINS, the DYNORPHINS, and the ENDORPHINS. Each of these families derives from different precursors, proenkephalin, prodynorphin, and PRO-OPIOMELANOCORTIN, respectively. There are also at least three classes of OPIOID RECEPTORS, but the peptide families do not map to the receptors in a simple way.
    
			 
				
				
					
						| Descriptor ID | D018847 |  
						| MeSH Number(s) | D12.644.400.575 D12.776.631.650.575 |  
						| Concept/Terms | Opioid PeptidesOpioid PeptidesPeptides, OpioidOpiate PeptidesPeptides, OpiateOpioid PeptidePeptide, Opioid
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				Below are MeSH descriptors whose meaning is more general than "Opioid Peptides". 
				Below are MeSH descriptors whose meaning is more specific than "Opioid Peptides". 
	
	
		
			
			
					
				This graph shows the total number of publications written about "Opioid Peptides" by people in this website by year, and whether "Opioid Peptides" was a major or minor topic of these publications.  
					  To see the data from this visualization as text, click here. 
		            | Year | Major Topic | Minor Topic | Total | 
|---|
 | 1997 | 1 | 0 | 1 |  | 1999 | 1 | 0 | 1 |  | 2000 | 0 | 1 | 1 |  | 2010 | 1 | 0 | 1 |  | 2014 | 0 | 3 | 3 |  | 2020 | 1 | 1 | 2 | 
 
                    To return to the timeline, click here. 
				Below are the most recent publications written about "Opioid Peptides" by people in Profiles. 		
					
								
								Bagley EE, Ingram SL. Endogenous opioid peptides in the descending pain modulatory circuit. Neuropharmacology. 2020 08 15; 173:108131.
								Sapio MR, Iadarola MJ, Loydpierson AJ, Kim JJ, Thierry-Mieg D, Thierry-Mieg J, Maric D, Mannes AJ. Dynorphin and Enkephalin Opioid Peptides and Transcripts in Spinal Cord and Dorsal Root Ganglion During Peripheral Inflammatory Hyperalgesia and Allodynia. J Pain. 2020 Sep - Oct; 21(9-10):988-1004.
								Li MH, Suchland KL, Ingram SL. GABAergic transmission and enhanced modulation by opioids and endocannabinoids in adult rat rostral ventromedial medulla. J Physiol. 2015 Jan 01; 593(1):217-30.
								Macey TA, Bobeck EN, Suchland KL, Morgan MM, Ingram SL. Change in functional selectivity of morphine with the development of antinociceptive tolerance. Br J Pharmacol. 2015 Jan; 172(2):549-61.
								Woods IG, Schoppik D, Shi VJ, Zimmerman S, Coleman HA, Greenwood J, Soucy ER, Schier AF. Neuropeptidergic signaling partitions arousal behaviors in zebrafish. J Neurosci. 2014 Feb 26; 34(9):3142-60.
								Dasgupta N, Freifeld C, Brownstein JS, Menone CM, Surratt HL, Poppish L, Green JL, Lavonas EJ, Dart RC. Crowdsourcing black market prices for prescription opioids. J Med Internet Res. 2013 Aug 16; 15(8):e178.
								Macey TA, Ingram SL, Bobeck EN, Hegarty DM, Aicher SA, Arttamangkul S, Morgan MM. Opioid receptor internalization contributes to dermorphin-mediated antinociception. Neuroscience. 2010 Jun 30; 168(2):543-50.
								Robertson LJ, Hammond GR, Drummond PD. The effect of subcutaneous naloxone on experimentally induced pain. J Pain. 2008 Jan; 9(1):79-87.
								Frew AK, Drummond PD. Negative affect, pain and sex: the role of endogenous opioids. Pain. 2007 Nov; 132 Suppl 1:S77-S85.
								Ingram SL. Cellular and molecular mechanisms of opioid action. Prog Brain Res. 2000; 129:483-92. | 
																	
																		
																			
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