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Ephedrine

Drugs and Chemicals · NLM MeSH · updated 2026-10-31 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 5 min read

A phenethylamine found in ephedra sinica.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (854 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

A phenethylamine found in ephedra sinica. pseudoephedrine is an isomer. It is an alpha- and beta-adrenergic agonist that may also enhance release of norepinephrine. It has been used for asthma, heart failure, rhinitis, and urinary incontinence, and for its central nervous system stimulatory effects in the treatment of narcolepsy and depression. It has become less extensively used with the advent of more selective agonists.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Erythro Isomer of Ephedrine; Ephedrine Erythro Isomer; Sal-Phedrine; SalPhedrine; Sal Phedrine; Ephedrine Sulfate; Sulfate, Ephedrine; Ephedrine Renaudin.

Where it fits in the MeSH classification

Broader topics
Propanolamines; Phenethylamines

Related concepts

  • Ephedra Sinica
  • Pseudoephedrine

Research landscape

PubMed indexes 5,034 records tagged with the MeSH heading “Ephedrine” (counts retrieved 2026-10-31). 231 of them (4.6%) were published from 2020 onward, and the busiest period so far is through 1999 with 3,302 records.

Reviews account for 248 records (4.9%) and meta-analyses for 23. Randomized controlled trials number 519 (10.3%) as a share of all records on the topic. Randomized trials make up a comparatively large share of this literature, which means many treatment questions have been tested directly.

PubMed records by publication periodthrough 1999: 3,302 records; 2000-2009: 989 records; 2010-2019: 512 records; 2020 onward: 231 records3,302through 19999892000-20095122010-20192312020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 19993,302
2000-2009989
2010-2019512
2020 onward231
Share of records by publication typeReviews: 4.9 percent; Meta-analyses: 0.5 percent; Randomized controlled trials: 10.3 percentReviews4.9% (248)Meta-analyses0.5% (23)Randomized controlled trials10.3% (519)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 5,034 PubMed records
TypeRecordsShare
Reviews2484.9%
Meta-analyses230.5%
Randomized controlled trials51910.3%

Method: PubMed query "Ephedrine"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in drugs and chemicals

Studies of a chemical or drug can answer very different questions: what it is and how it behaves in cells and animals, how the body handles it, and whether it changes outcomes in people. Laboratory and animal findings often do not carry over to patients, and observational studies of exposures are confounded by who uses a substance and why. Nothing on this page is a recommendation to use, avoid, start or stop any substance or medicine; talk to a qualified clinician or pharmacist about your own situation. Check the dose, the species, the comparison group and whether a patient-relevant outcome was measured.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Ephedrine alkaloids-free Ephedra Herb extract: a safer alternative to ephedra with comparable analgesic, anticancer, and anti-influenza activities
Hyuga S, Hyuga M, Oshima N, Maruyama T, Kamakura H, Yamashita T, et al.
2016Research article
Design not recorded in structured metadata
57cc by
PMID 26943796 · DOI · PMC4935746
p-Synephrine, ephedrine, p-octopamine and m-synephrine: Comparative mechanistic, physiological and pharmacological properties
Stohs SJ, Shara M, Ray SD
2020Review article
Design not recorded in structured metadata
35cc by
PMID 32101364 · DOI · PMC7496387
Efficiently prepared ephedrine alkaloids-free Ephedra Herb extract: a putative marker and antiproliferative effects
Oshima N, Yamashita T, Hyuga S, Hyuga M, Kamakura H, Yoshimura M, et al.
2016Research article
Design not recorded in structured metadata
34cc by
PMID 26976141 · DOI · PMC4935757
11C-Hydroxyephedrine PET/CT for preoperative surgical planning in large pheochromocytoma and paraganglioma
Vyakaranam AR, Norlén O, Akural A, Crona J, Annebäck M, Klimàcek B, et al.
2026Research article
Design not recorded in structured metadata
1cc by
PMID 41319260 · DOI · PMC12799324

Ephedrine alkaloids-free Ephedra Herb extract: a safer alternative to ephedra with comparable analgesic, anticancer, and anti-influenza activities [1]

Research article Hyuga S, Hyuga M, Oshima N, Maruyama T, Kamakura H, Yamashita T, et al. · · 2016 · cited 57 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
It is generally accepted that the primary pharmacological activities and adverse effects of Ephedra Herb are caused by ephedrine alkaloids.
Closing excerpt
Therefore, EFE could be a useful pharmacological agent.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (202 words)

It is generally accepted that the primary pharmacological activities and adverse effects of Ephedra Herb are caused by ephedrine alkaloids. Interestingly, our research shows that Ephedra Herb also has ephedrine alkaloid-independent pharmacological actions, such as c-MET inhibitory activity. This study describes the preparation of an ephedrine alkaloids-free Ephedra Herb extract (EFE) by ion-exchange column chromatography, as well as in vitro and in vivo evaluation of its pharmacological actions and toxicity. We confirmed that EFE suppressed hepatocyte growth factor (HGF)-induced cancer cell motility by preventing both HGF-induced phosphorylation of c-Met and its tyrosine kinase activity. We also investigated the analgesic effect of EFE. Although the analgesic effect of Ephedra Herb has traditionally been attributed to pseudoephedrine, oral administration of EFE reduced formalin-induced pain in a dose-dependent manner in mice. Furthermore, we confirmed the anti-influenza virus activity of EFE by showing inhibition of MDCK cell infection in a concentration-dependent manner. All assessments of toxicity, even after repeated oral administration, suggest that EFE would be a safer alternative to Ephedra Herb. The findings described here suggest that EFE has c-Met inhibitory action, analgesic effect, and anti-influenza activity, and that it is safer than Ephedra Herb extract itself. Therefore, EFE could be a useful pharmacological agent.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 26943796 · DOI · PMC4935746

p-Synephrine, ephedrine, p-octopamine and m-synephrine: Comparative mechanistic, physiological and pharmacological properties [2]

Review article Stohs SJ, Shara M, Ray SD · · 2020 · cited 35 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Confusion and misunderstanding exist regarding the lack of cardiovascular and other adverse health effects of p-synephrine and p-octopamine relative to ephedrine and m-synephrine (phenylephrine) which are known for their effects on the cardiovascular system.
Closing excerpt
These conclusions are supported by human, animal and in vitro studies that are discussed.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (180 words)

Confusion and misunderstanding exist regarding the lack of cardiovascular and other adverse health effects of p-synephrine and p-octopamine relative to ephedrine and m-synephrine (phenylephrine) which are known for their effects on the cardiovascular system. These four molecules have some structural similarities. However, the structural and stereochemical differences of p-synephrine and p-octopamine as related to ephedrine and m-synephrine result in markedly different adrenergic receptor binding characteristics as well as other mechanistic differences which are reviewed. p-Synephrine and p-octopamine exhibit little binding to α-1, α-2, β-1 and β-2 adrenergic receptors, nor are they known to exhibit indirect actions leading to an increase in available levels of endogenous norepinephrine and epinephrine at commonly used doses. The relative absence of these mechanistic actions provides an explanation for their lack of production of cardiovascular effects at commonly used oral doses as compared to ephedrine and m-synephrine. As a consequence, the effects of ephedrine and m-synephrine cannot be directly extrapolated to p-synephrine and p-octopamine which exhibit significantly different pharmacokinetic, and physiological/pharmacological properties. These conclusions are supported by human, animal and in vitro studies that are discussed.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 32101364 · DOI · PMC7496387

Efficiently prepared ephedrine alkaloids-free Ephedra Herb extract: a putative marker and antiproliferative effects [3]

Research article Oshima N, Yamashita T, Hyuga S, Hyuga M, Kamakura H, Yoshimura M, et al. · · 2016 · cited 34 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Ephedrine alkaloids (EAs) have been considered the main pharmacologically active substances in Ephedra Herb (, Mao; EH) since they were first identified by Prof.
Closing excerpt
These results indicate that EFE retained the anticancer effect of EH and demonstrated its potential for future development as a new herbal medicine with reduced side effects.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (235 words)

Ephedrine alkaloids (EAs) have been considered the main pharmacologically active substances in Ephedra Herb (, Mao; EH) since they were first identified by Prof. N. Nagai, and are known to induce palpitation, hypertension, insomnia, and dysuria as side effects. Therefore, the administration of drugs containing EH to patients with cardiovascular-related diseases is severely contraindicated. While our previous studies suggest that some of the effects of EH may not be due to EAs, considering their side effects would be expedient to develop a new EAs-free EH extract (EFE). Here, we established a preparation method for EFE and revealed its chemical composition, including the content of herbacetin, a flavonoid aglycon present in EH and a potential putative marker for EFE quality control. In addition, we showed the antiproliferative effects of EFE against the H1975 non-small cell lung cancer (NSCLC) cell line. EFE was prepared from EH extract using the ion exchange resin SK-1B. LC/Orbitrap MS analysis revealed the removal of EAs, 6-methoxykynurenic acid, and 6-hydroxykynurenic acid from the original extract. Quantitative analysis of herbacetin using LC/MS in acid-hydrolyzed EFE showed that its content was 0.104 %. Although several alkaloidal constituents were removed from EH extract, the antiproliferative effect of EFE against H1975 cells was comparable to that of EH extract. These results indicate that EFE retained the anticancer effect of EH and demonstrated its potential for future development as a new herbal medicine with reduced side effects.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 26976141 · DOI · PMC4935757

11C-Hydroxyephedrine PET/CT for preoperative surgical planning in large pheochromocytoma and paraganglioma [4]

Research article Vyakaranam AR, Norlén O, Akural A, Crona J, Annebäck M, Klimàcek B, et al. · · 2026 · cited 1 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Early detection of metastases and timely surgical intervention play a crucial role in the management of neuroendocrine tumors.
Closing excerpt
These findings suggest that HED-PET/CT is highly accurate in detecting metastases; however, its routine preoperative use may be limited and appears to provide significant clinical benefit only in selected patients.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (237 words)

Early detection of metastases and timely surgical intervention play a crucial role in the management of neuroendocrine tumors. In large-sized pheochromocytomas and sympathetic paragangliomas (PPGL), functional imaging with positron emission tomography (PET) is recommended, as it improves the detection of metastases, which may go undetected on conventional radiologic imaging. 11C-hydroxyephedrine binds to the norepinephrine transporter receptor and is detected by PET/CT (HED-PET/CT). It has previously demonstrated high accuracy in detecting primary and metastatic PPGL; however, its impact on preoperative staging is unclear. In this study, we retrospectively analyzed a selected cohort of 44 patients with large PPGL to evaluate whether HED-PET/CT influences preoperative clinical decision-making. All patients who underwent HED-PET/CT at Uppsala University Hospital between 2004 and 2024 were screened for inclusion. In total, 44 patients with pheochromocytomas >5 cm and paragangliomas >4 cm were included. HED-PET/CT results were compared with CT/MR findings, and a final consensus was reached on whether preoperative HED-PET/CT would have altered clinical decision-making. HED-PET/CT identified previously undetected metastatic disease in three patients (6.8%), which had not been visualized on CT/MR. Additionally, two patients had discordant findings, where HED-PET/CT revealed additional metastases. In one case, a liver metastasis was identified postoperatively with HED-PET/CT, leading to a metastasectomy that could have potentially been avoided. These findings suggest that HED-PET/CT is highly accurate in detecting metastases; however, its routine preoperative use may be limited and appears to provide significant clinical benefit only in selected patients.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41319260 · DOI · PMC12799324

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Efficacy and safety of ephedra and ephedrine for weight loss and athletic performance: a meta-analysis [5]
    Shekelle PG, Hardy ML, Morton SC, Maglione M, Mojica WA, Suttorp MJ, et al. · JAMA · 2003 · cited 250 times (Europe PMC)
  • Research article A quantitative, systematic review of randomized controlled trials of ephedrine versus phenylephrine for the management of hypotension during spinal anesthesia for cesarean delivery [6]
    Lee A, Ngan Kee WD, Gin T · Anesth Analg · 2002 · cited 219 times (Europe PMC)
  • Research article Obesity and thermogenesis related to the consumption of caffeine, ephedrine, capsaicin, and green tea [7]
    Diepvens K, Westerterp KR, Westerterp-Plantenga MS · Am J Physiol Regul Integr Comp Physiol · 2007 · cited 168 times (Europe PMC)
  • Research article Ephedra in perspective--a current review [8]
    Abourashed EA, El-Alfy AT, Khan IA, Walker L · Phytother Res · 2003 · cited 123 times (Europe PMC)
  • Research article Acute hepatitis associated with the use of a Chinese herbal product, ma-huang [9]
    Nadir A, Agrawal S, King PD, Marshall JB · Am J Gastroenterol · 1996 · cited 97 times (Europe PMC)
  • Research article A review of the impact of phenylephrine administration on maternal hemodynamics and maternal and neonatal outcomes in women undergoing cesarean delivery under spinal anesthesia [10]
    Habib AS · Anesth Analg · 2012 · cited 96 times (Europe PMC)

References

  1. Hyuga S, Hyuga M, Oshima N, Maruyama T, Kamakura H, Yamashita T, et al.. Ephedrine alkaloids-free Ephedra Herb extract: a safer alternative to ephedra with comparable analgesic, anticancer, and anti-influenza activities. . 2016. PMID 26943796 · DOI · PMC4935746
  2. Stohs SJ, Shara M, Ray SD. p-Synephrine, ephedrine, p-octopamine and m-synephrine: Comparative mechanistic, physiological and pharmacological properties. . 2020. PMID 32101364 · DOI · PMC7496387
  3. Oshima N, Yamashita T, Hyuga S, Hyuga M, Kamakura H, Yoshimura M, et al.. Efficiently prepared ephedrine alkaloids-free Ephedra Herb extract: a putative marker and antiproliferative effects. . 2016. PMID 26976141 · DOI · PMC4935757
  4. Vyakaranam AR, Norlén O, Akural A, Crona J, Annebäck M, Klimàcek B, et al.. 11C-Hydroxyephedrine PET/CT for preoperative surgical planning in large pheochromocytoma and paraganglioma. . 2026. PMID 41319260 · DOI · PMC12799324
  5. Shekelle PG, Hardy ML, Morton SC, Maglione M, Mojica WA, Suttorp MJ, et al.. Efficacy and safety of ephedra and ephedrine for weight loss and athletic performance: a meta-analysis. JAMA. 2003. PMID 12672771 · DOI
  6. Lee A, Ngan Kee WD, Gin T. A quantitative, systematic review of randomized controlled trials of ephedrine versus phenylephrine for the management of hypotension during spinal anesthesia for cesarean delivery. Anesth Analg. 2002. PMID 11916798 · DOI
  7. Diepvens K, Westerterp KR, Westerterp-Plantenga MS. Obesity and thermogenesis related to the consumption of caffeine, ephedrine, capsaicin, and green tea. Am J Physiol Regul Integr Comp Physiol. 2007. PMID 16840650 · DOI
  8. Abourashed EA, El-Alfy AT, Khan IA, Walker L. Ephedra in perspective--a current review. Phytother Res. 2003. PMID 12916063 · DOI
  9. Nadir A, Agrawal S, King PD, Marshall JB. Acute hepatitis associated with the use of a Chinese herbal product, ma-huang. Am J Gastroenterol. 1996. PMID 8678010
  10. Habib AS. A review of the impact of phenylephrine administration on maternal hemodynamics and maternal and neonatal outcomes in women undergoing cesarean delivery under spinal anesthesia. Anesth Analg. 2012. PMID 22104076 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-31.

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At a glance

5,034
PubMed records on this heading
5%
published since 2020
248
review articles
519
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

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