Evidence map›Paper›PMID 33212113›Full record

ReviewNeuropharmacology2021

Hemopressin as a breakthrough for the cannabinoid field.

Andrea S Heimann, Camila S Dale, Francisco S Guimarães, Ricardo A M Reis, Ami Navon, Michal A Shmuelov, Vanessa Rioli, Ivone Gomes, Lakshmi L Devi, Emer S Ferro

Open access · greenAbstract readReview
In one paragraph

Review in Neuropharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Genetic Tools in Rodents to Study Cannabinoid Functions.Current topics in behavioral neurosciences · 2026
    Review
  3. Article
  4. Article
  5. Current Challenges and Future Directions in Peptidomics.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Microglial Cannabinoid CBInternational journal of molecular sciences · 2023
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 3 countries.

Andrea S HeimannProteimax Israel Biotechnology, Rehovot, 7610001, Israel. Electronic address: andrea@proteimax.com.
Camila S DaleDepartment of Anatomy, Biomedical Science Institute, University of São Paulo, 05508-000, São Paulo, SP, Brazil.
Francisco S GuimarãesDepartment of Pharmacology, Ribeirão Preto Medical School, University of São Paulo, 14025-600, Ribeirão Preto, SP, Brazil; Department of Neuroscience and Behavior, Ribeirão Preto Medical School, University of São Paulo, 14025-600, Ribeirão Preto, SP, Brazil.
Ricardo A M ReisLaboratory of Neurochemistry, Institute of Biophysics Carlos Chagas Filho, Rio de Janeiro, Federal University, 21949-900, Rio de Janeiro, RJ, Brazil.
Ami NavonDepartment of Biological Regulation, The Weizmann Institute of Science, Rehovot, 7610001, Israel.
Michal A ShmuelovDepartment of Biological Regulation, The Weizmann Institute of Science, Rehovot, 7610001, Israel.
Vanessa RioliSpecial Laboratory of Applied Toxinology (LETA), Center of Toxins, Immune Response and Cell Signaling (CETICS), Butantan Institute, São Paulo, 05503-900, Brazil.
Ivone GomesDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, 10029, New York, NY, United States.
Lakshmi L DeviDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, 10029, New York, NY, United States.
Emer S FerroDepartment of Biological Regulation, The Weizmann Institute of Science, Rehovot, 7610001, Israel; Department of Pharmacology, Biomedical Science Institute, University of São Paulo, 05508-000, São Paulo, SP, Brazil. Electronic address: eferro@usp.br.
Universidade de São Paulo · BRIcahn School of Medicine at Mount Sinai · USWeizmann Institute of Science · ILFundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro · BRInstituto Butantan · BR

Funding

Enzymes Involved in Neuropeptide Biosynthesis, Processing and RegulationR01NS026880 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DEVI, LAKSHMI A · 1994 to 2019
$6.5M
Regulation Of Opioid Receptor Signaling by Endogenous PeptidesR01DA008863 · NIDA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Lakshmi A Devi, Elyssa Margolis · 1995 to 2026
$6.1M
Post-translational Regulation of Opioid and Cannabinoid Receptors.R37DA008863 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DEVI, LAKSHMI A · 2012 to 2021
$4.6M
Post-translational regulation of opioid receptorsR56DA008863 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DEVI, LAKSHMI A · 2007 to 2007
$381k
NIDA NIH HHS R01 DA008863NIDA NIH HHS R37 DA008863NIDA NIH HHS R56 DA008863NINDS NIH HHS R01 NS026880
6 · The paper itself

Abstract

Hemopressin (PVNFKFLSH in rats, and PVNFKLLSH in humans and mice), a fragment derived from the α-chain of hemoglobin, was the first peptide described to have type 1 cannabinoid receptor activity. While hemopressin was shown to have inverse agonist/antagonistic activity, extended forms of hemopressin (i.e. RVD-hemopressin, also called pepcan-12) exhibit type 1 and type 2 cannabinoid receptor agonistic/allosteric activity, and recent studies suggest that they can activate intracellular mitochondrial cannabinoid receptors. Therefore, hemopressin and hemopressin-related peptides could have location-specific and biased pharmacological action, which would increase the possibilities for fine-tunning and broadening cannabinoid receptor signal transduction. Consistent with this, hemopressins were shown to play a role in a number of physiological processes including antinociceptive and anti-inflammatory activity, regulation of food intake, learning and memory. The shortest active hemopressin fragment, NFKF, delays the first seizure induced by pilocarpine, and prevents neurodegeneration in an experimental model of autoimmune encephalomyelitis. These functions of hemopressins could be due to engagement of both cannabinoid and non-cannabinoid receptor systems. Self-assembled nanofibrils of hemopressin have pH-sensitive switchable surface-active properties, and show potential as inflammation and cancer targeted drug-delivery systems. Upon disruption of the self-assembled hemopressin nanofibril emulsion, the intrinsic analgesic and anti-inflammatory properties of hemopressin could help bolster the therapeutic effect of anti-inflammatory or anti-cancer formulations. In this article, we briefly review the molecular and behavioral pharmacological properties of hemopressins, and summarize studies on the intricate and unique mode of generation and binding of these peptides to cannabinoid receptors. Thus, the review provides a window into the current status of hemopressins in expanding the repertoire of signaling and activity by the endocannabinoid system, in addition to their new potential for pharmaceutic formulations.

Indexed as

AnimalsCannabinoid Receptor AgonistsEndocannabinoidsHemoglobinsHumansMicePeptide FragmentsRatsReceptors, CannabinoidCannabinoid Receptor AgonistsEndocannabinoidsHemoglobinshemopressinPeptide FragmentsReceptors, CannabinoidCannabinoidCannabinoid receptorsEndocannabinoidHemopressin

Identifiers

PMID33212113
PMCPMC8609950
OpenAlexW3100301730

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.