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a potent narcotic antagonist (trade name Narcan) especially effective with morphine (同)Narcan

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2018/09/18 20:29:08」(JST)

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Naloxone, sold under the brandname Narcan among others, is a medication used to block the effects of opioids, especially in overdose.^[1] Naloxone may be combined with an opioid (in the same pill) to decrease the risk of misuse.^[1] When given intravenously, naloxone works within two minutes, and when injected into a muscle, it works within five minutes;^[1] it may also be sprayed into the nose.^[3] The effects of naloxone last about half an hour to an hour.^[4] Multiple doses may be required, as the duration of action of most opioids is greater than that of naloxone.^[1]

Administration to opioid-dependent individuals may cause symptoms of opioid withdrawal, including restlessness, agitation, nausea, vomiting, a fast heart rate, and sweating.^[1] To prevent this, small doses every few minutes can be given until the desired effect is reached.^[1] In those with previous heart disease or taking medications that negatively affect the heart, further heart problems have occurred.^[1] It appears to be safe in pregnancy, after having been given to a limited number of women.^[5] Naloxone is a non-selective and competitive opioid receptor antagonist.^[6]^[7] It works by reversing the depression of the central nervous system and respiratory system caused by opioids.^[1]

Naloxone was patented in 1961 and approved for opioid overdose by the Food and Drug Administration in 1971.^[8] It is on the World Health Organization's List of Essential Medicines, the most effective and safe medicines needed in a health system.^[9] Naloxone is available as a generic medication.^[1] Its wholesale price in the developing world is between $0.50 and $5.30 per dose.^[10] Vials of naloxone are not very expensive (less than $25) in the United States.^[11] The price for a package of two auto-injectors in the US, however, has increased from $690 in 2014 to $4,500 in 2016.^[12] The 2018 price for the NHS in the United Kingdom is about £5 per dose.^[13]

1 Medical uses
- 1.1 Opioid overdose
- 1.2 Preventing opioid abuse
- 1.3 Other uses
- 1.4 Routes of administration
2 Special populations
- 2.1 Pregnancy and breastfeeding
- 2.2 Kidney and liver dysfunction
- 2.3 Cardiovascular disease
3 Side effects
4 Pharmacology
- 4.1 Pharmacodynamics
- 4.2 Pharmacokinetics
5 Chemistry
6 History
7 Society and culture
- 7.1 Names
- 7.2 Legal status
- 7.3 Prehospital access
- 7.4 Identification
- 7.5 Media
8 See also
9 References
10 External links

Medical uses

Opioid overdose

A naloxone kit as distributed in British Columbia, Canada

Naloxone is useful both in acute opioid overdose and in reducing respiratory or mental depression due to opioids.^[1] Whether it is useful in those in cardiac arrest due to an opioid overdose is unclear.^[14]

It is included as a part of emergency overdose response kits distributed to heroin and other opioid drug users and emergency responders. This has been shown to reduce rates of deaths due to overdose.^[15] A prescription for naloxone is recommended if a person is on a high dose of opioid (>100 mg of morphine equivalence/day), is prescribed any dose of opioid accompanied by a benzodiazepine, or is suspected or known to use opioids nonmedically.^[16] Prescribing naloxone should be accompanied by standard education that includes preventing, identifying, and responding to an overdose; rescue breathing; and calling emergency services.^[17]

Preventing opioid abuse

Naloxone is poorly absorbed when taken by mouth, so it is commonly combined with a number of oral opioid preparations, including buprenorphine and pentazocine, so that when taken orally, just the opioid has an effect, but if misused by injecting, the naloxone blocks the effect of the opioid.^[1]^[18] This combination is used in an effort to prevent abuse.^[18] In Germany, tilidine is sold in a fixed combination with naloxone.

Other uses

Naloxone can be used on infants that were exposed to intrauterine opiates administered to mothers during delivery. However, there is insufficient evidence for the use of naloxone to lower cardiorespiratory and neurological depression in these infants.^[19] Infants exposed to high concentrations of opiates during pregnancy may have CNS damage in the setting of perinatal asphyxia. Naloxone has been studied to improve outcomes in this population, however the evidence is currently weak.^[20]

In people with shock, including septic, cardiogenic, hemorrhagic, or spinal shock, those who received naloxone had improved blood flow. The importance of this is unclear.^[21]

Naloxone is also experimentally used in the treatment for congenital insensitivity to pain with anhidrosis, an extremely rare disorder (one in 125 million) that renders one unable to feel pain or differentiate temperatures.^{[citation needed]}

Naloxone can also be used as an antidote in overdose of clonidine, a medication that lowers blood pressure.^[22]

Naloxone can also be used to treat itchiness brought on by opioid use.^[23]

Routes of administration

Naloxone is most commonly injected intravenously for fastest action, which usually causes the drug to act within a minute, and lasts up to 45 minutes. It can also be administered via intramuscular, subcutaneous injection, or nasal spray.^[24] There is a prepackaged nasal spray that does not require assembly and delivers a consistent dose.^[25] It can be repeated if necessary.^[26] A non-FDA approved wedge device (nasal atomizer) attached to a syringe may be used to create a mist that delivers the drug to the nasal mucosa.^[27] This is useful near facilities where many overdoses occur that already stock injectors.^[28]

If minimal or no response is observed within 2–3 minutes, dosing may be repeated every 2 minutes until the maximum dose of 10 mg has been reached. If no response occurs at this time, alternative diagnosis and treatment should be pursued. The effects of naloxone may wear off before those of the opioids, and they may require repeat dosing at a later time. Patients experiencing effects should be monitored for respiratory rate, heart rate, blood pressure, temperature, ABGs and level of consciousness. Those with a greater risk for respiratory depression should be identified prior to administration and watched closely.^[29]

In April 2014, the US Food and Drug Administration (FDA) approved a hand-held automatic injector naloxone product that is pocket-sized and can be used in nonmedical settings such as in the home.^[30] It is designed for use by laypersons, including family members and caregivers of opioid users at-risk for an opioid emergency, such as an overdose.^[31] A nasal spray was developed in a partnership between LightLake Therapeutics and the National Institute on Drug Abuse.^[32] The approval process was fast-tracked as one initiative to reduce the death toll caused by opiate overdoses. At the time of approval, an estimated 16,000 annual deaths were attributed to prescription opioid overdoses in the US.^[33]

Naloxone can be used along with oxycodone controlled release and may help reduce constipation associated with opioids. Naloxone has low systemic bioavailability when taken by mouth due to hepatic first pass metabolism, but it does block opioid receptors that are located in the intestine.^[34]

Special populations

Pregnancy and breastfeeding

Naloxone is pregnancy category B or C in the United States.^[1] Studies in rodents given a daily maximum dose of 10 mg naloxone showed no harmful effects to the fetus, although human studies are lacking and the drug does cross the placenta, which may lead to the precipitation of withdrawal in the fetus. In this setting, further research is needed before safety can be assured, so naloxone should only be used during pregnancy if it is a medical necessity.^[35]

Whether naloxone is excreted in breast milk is unknown, however, it is not orally bioavailable and therefore is unlikely to affect a breastfeeding infant.^[36]

Kidney and liver dysfunction

Currently, no established clinical trials have been conducted in person with insufficient kidney function or liver disease, and as such, these people should be monitored closely if naloxone is clinically indicated.

Cardiovascular disease

Naloxone should be used with caution in people with cardiovascular disease as well as those that are currently taking medications that could have adverse effects on the cardiovascular system such as causing low blood pressure, fluid accumulation in the lungs (pulmonary edema), and abnormal heart rhythms. There have been reports of abrupt reversals with opioid antagonists leading to pulmonary edema and ventricular fibrillation.^[37]

Side effects

Naloxone has little to no effect if opioids are not present. In people with opioids in their system, it may cause increased sweating, nausea, restlessness, trembling, vomiting, flushing, and headache, and has in rare cases been associated with heart rhythm changes, seizures, and pulmonary edema.^[38]^[39]

Besides the side effects listed above, naloxone also has other adverse events, such as other cardiovascular effects (hypertension, hypotension, tachycardia, ventricular fibrillation, ventricular tachycardia) and central nervous system effects, such as agitation, body pain, brain disease, and coma. In addition to these adverse effects, naloxone is also contraindicated in people with hypersensitivity to naloxone or any of its formulation components.^[40]

Naloxone has been shown to block the action of pain-lowering endorphins which the body produces naturally. These endorphins likely operate on the same opioid receptors that naloxone blocks. It is capable of blocking a placebo pain-lowering response, if the placebo is administered together with a hidden or blind injection of naloxone.^[41] Other studies have found that placebo alone can activate the body's μ-opioid endorphin system, delivering pain relief by the same receptor mechanism as morphine.^[42]^[43]

Pharmacology

Pharmacodynamics

Naloxone at opioid receptors
Compound	Affinities (K_i)			Ratio	Ref
Compound	MOR	DOR	KOR	MOR:DOR:KOR	Ref
Naloxone	1.1 nM	16 nM	12 nM	1:15:11	^[44]
(−)-Naloxone	0.559 nM 0.93 nM	36.5 nM 17 nM	4.91 nM 2.3 nM	1:65:9 1:18:2	^[45] ^[46]
(+)-Naloxone	3,550 nM >1,000 nM	122,000 nM >1,000 nM	8,950 nM >1,000 nM	1:34:3 ND	^[45] ^[46]

Naloxone is a lipophilic compound that acts as a non-selective and competitive opioid receptor antagonist.^[6]^[7] The pharmacologically active isomer of naloxone is (−)-naloxone.^[45]^[47] Naloxone's binding affinity is highest for the μ-opioid receptor, then the δ-opioid receptor, and lowest for the κ-opioid receptor;^[6] naloxone has negligible affinity for the nociceptin receptor.^[48]

If naloxone is administered in the absence of concomitant opioid use, no functional pharmacological activity occurs, except the inability for the body to combat pain naturally. In contrast to direct opiate agonists, which elicit opiate withdrawal symptoms when discontinued in opiate-tolerant people, no evidence indicates the development of tolerance or dependence on naloxone. The mechanism of action is not completely understood, but studies suggest it functions to produce withdrawal symptoms by competing for opiate receptor sites within the CNS (a competitive antagonist, not a direct agonist), thereby preventing the action of both endogenous and xenobiotic opiates on these receptors without directly producing any effects itself.^[49]

Pharmacokinetics

When administered parenterally (nonorally or nonrectally, e.g. intravenously or by injection), as is most common, naloxone has a rapid distribution throughout the body. The mean serum half life has been shown to range from 30 to 81 minutes, shorter than the average half life of some opiates, necessitating repeat dosing if opioid receptors must be stopped from triggering for an extended period. Naloxone is primarily metabolized by the liver. Its major metabolite is naloxone-3-glucuronide, which is excreted in the urine.^[49]

Chemistry

Naloxone, also known as N-allylnoroxymorphone or as 17-allyl-4,5α-epoxy-3,14-dihydroxymorphinan-6-one, is a synthetic morphinan derivative and was derived from oxymorphone (14-hydroxydihydromorphinone), an opioid analgesic.^[50]^[51]^[52] Oxymorphone, in turn, was derived from morphine, an opioid analgesic and naturally occurring constituent of the opium poppy.^[53] Naloxone is a racemic mixture of two enantiomers, (–)-naloxone (levonaloxone) and (+)-naloxone (dextronaloxone), only the former of which is active at opioid receptors.^[54]^[55] The drug is a highly lipophilic, allowing it to rapidly penetrate the brain and to achieve a far greater brain to serum ratio than that of morphine.^[50] Opioid antagonists related to naloxone include cyprodime, nalmefene, nalodeine, naloxol, and naltrexone.^[56]

History

Naloxone was patented in 1961 by Jack Fishman, Mozes J. Lewenstein, and the company Sankyo.^[8] It was approved for opioid abuse treatment in 1971 by the FDA with opioid abuse kits being distributed by many states to medically untrained people beginning in 1996. From the period of 1996 to 2014, the CDC estimates over 26,000 cases of opioid overdose have been reversed using the kits.^[57]

Society and culture

Names

Naloxone is the generic name of the drug and its INN, BAN, DCF, DCIT, and JAN, while naloxone hydrochloride is its USAN and BANM.^[58]^[59]^[60]^[61]

The patent for naloxone has expired; consequently, it is available in generic medication. Brand names of naloxone include Narcan, Nalone, Evzio, Prenoxad Injection, Narcanti, Narcotan, and others.

Legal status

In the United States, naloxone is classified as a prescription medication, though it is not a controlled substance.^[62] While it is legal to prescribe naloxone in every state, dispensing the drug by medical professionals (including physicians or other licensed prescribers) at the point of service is subject to rules that vary by jurisdiction. In the following states, it is possible to purchase naloxone from a pharmacist directly without getting a prescription from a doctor: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Minnesota, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Vermont, Washington, West Virginia and Wisconsin.^[63] However depending on the pharmacy a pharmacist may have to write a prescription or not be able to give naloxone to comply with accounting rules regarding prescription medications as naloxone is still considered a prescription only medication under FDA rules.

While paramedics have carried naloxone for decades, law enforcement officers in many states throughout the country carry naloxone to reverse the effects of heroin overdoses when reaching the location prior to paramedics. As of July 12, 2015, law enforcement departments in 28 states are allowed to or required to carry naloxone to quickly respond to opioid overdoses.^[64]

In Australia, as of February 1, 2016, naloxone is now available "over the counter" in pharmacies without a prescription.^[65] It comes in single use filled syringe similar to law enforcement kits.

In Canada, naloxone single-use syringe kits are distributed and available at various clinics and emergency rooms. Alberta Health Services is increasing the distribution points for naloxone kits at all emergency rooms, and various pharmacies and clinics province-wide. Also in Alberta, take-home naloxone kits are available and commonly distributed in most drug treatment or rehabilitation centres, as well as in pharmacies where pharmacists can distribute single-use take-home naloxone kits or prescribe the drug to addicts. All Edmonton Police Service and Calgary Police Service patrol cars carry an emergency single-use naloxone syringe kit. Some Royal Canadian Mounted Police patrol vehicles also carry the drug, occasionally in excess to help distribute naloxone among users and concerned family/friends. Nurses, paramedics, medical technicians, and emergency medical responders can also prescribe and distribute the drug.

Following Alberta Health Services, Health Canada reviewed the prescription-only status of naloxone, resulting in plans to remove it in 2016, allowing naloxone to be more accessible.^[66]^[67] Due to the rising number of drug deaths across the country, Health Canada proposed a change to make naloxone more widely available to Canadians in support of efforts to address the growing number of opioid overdoses.^[68] In March 2016, Health Canada did change the prescription status of naloxone, as "pharmacies are now able to proactively give out naloxone to those who might experience or witness an opioid overdose."^[69]

Prehospital access

Laws in many jurisdictions have been changed in recent years to allow wider distribution of naloxone.^[70]^[71] Several states have also moved to permit pharmacies to dispense the medication without the person first seeing a physician or other non-pharmacist professional.^[72] Over 200 naloxone distribution programs utilize licensed prescribers to distribute the drug, often through the use of standing medication orders ^[73]^[74] whereby the medication is distributed under the medical authority of a physician or other prescriber (such as a pharmacist under California's AB1535).

Following the use of the nasal spray device by police officers on Staten Island in New York, an additional 20,000 police officers will begin carrying naloxone in mid-2014. The state's Office of the Attorney General will provide US$1.2 million to supply nearly 20,000 kits. Police Commissioner William Bratton said: "Naloxone gives individuals a second chance to get help".^[75] Emergency Medical Service Providers (EMS) routinely administer naloxone, except where basic Emergency Medical Technicians are prohibited by policy or by state law.^[76]

A survey of US naloxone prescription programs in 2010 revealed that 21 out of 48 programs reported challenges in obtaining naloxone in the months leading up to the survey, due mainly to either cost increases that outstripped allocated funding or the suppliers' inability to fill orders.^[77] The approximate cost of a 1 ml ampoule of naloxone in the US is estimated to be significantly higher than in most Western countries.^[73]

Projects of this type are under way in many North American cities.^[77]^[78] CDC estimates that the US programs for drug users and their caregivers prescribing take-home doses of naloxone and training on its use have prevented 10,000 opioid overdose deaths.^[77] Healthcare institution-based naloxone prescription programs have also helped reduce rates of opioid overdose in North Carolina, and have been replicated in the US military.^[73]^[79] Programs training police and fire personnel in opioid overdose response using naloxone have also shown promise in the US, and effort is increasing to integrate opioid fatality prevention in the overall response to the overdose crisis.^[80]^[81]^[82]^[83]

Pilot projects were also started in Scotland in 2006. Also in the UK, in December 2008, the Welsh Assembly government announced its intention to establish demonstration sites for take-home naloxone.^[84]

As of February 2016, Pharmacies across Alberta and some other Canadian jurisdictions are allowed to distribute take-home naloxone kits. Additionally, the Minister of Health issued an order to change basic life support provider's medical scope, within EMS, to administer naloxone in the event of a suspected narcotic overdose. These are part of the government's plan to tackle a growing fentanyl drug crisis.^[85]

Identification

The CAS number of naloxone is 465-65-6; the anhydrous hydrochloride salt has CAS 357-08-4 and the hydrochloride salt with 2 molecules of water, hydrochloride dihydrate, has CAS 51481-60-8.

Media

The 2013 documentary film Reach for Me: Fighting to End the American Drug Overdose Epidemic interviews people involved in naloxone programs aiming to make naloxone available to opioid users and people with chronic pain.^[86]

References

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^ Louise A. Bennett (2006). New Topics in Substance Abuse Treatment. Nova Publishers. pp. 9–. ISBN 978-1-59454-831-4.
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^ "The History of Naloxone - Cordant Solutions". Cordant Solutions. 2017-07-05. Retrieved 2017-11-14.
^ J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 851–. ISBN 978-1-4757-2085-3.
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^ I.K. Morton; Judith M. Hall (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 189–. ISBN 978-94-011-4439-1.
^ https://www.drugs.com/international/naloxone.html
^ 21 U.S.C.A. §§801-904; see e.g., LA Rev Stat. Ann. §40:964 (specifically excluding Naloxone from the schedule of controlled substances.)
^ "Everything You Need to Know About Narcan". Ambrosia Treatment Center. 20 July 2016. Archived from the original on 2 March 2017. Retrieved 1 March 2017.
^ "US Law Enforcement Who Carry Naloxone". North Carolina Harm Reduction Coalition. Archived from the original on 13 July 2015. Retrieved 12 July 2015.
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^ Corey Davis. "Legal interventions to reduce overdose mortality: Naloxone access and overdose good samaritan laws" (PDF). Network for Public Health Law. Archived (PDF) from the original on 2014-09-03.
^ Davis CS, Webb D, Burris SC (2013). "Changing Law from Barrier to Facilitator of Opioid Overdose Prevention". Journal of Law, Medicine and Ethics.
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External links

Chicago Recovery Alliance's naloxone distribution project
Report on Naloxone and other opiate antidotes, by the International Programme on Chemical Safety
What Is Naloxone? via Substance Abuse and Mental Health Services Administration| SAMHSA
Naloxone Overdose Prevention Laws | PDAPS.org

UpToDate Contents

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1. 地域社会における、オピオイド過量投与による死亡の予防 prevention of lethal opioid overdose in the community
2. 麻酔後回復室（PACU）における心血管の障害 cardiovascular problems in the post anesthesia care unit pacu
3. オピオイド使用障害の薬物療法 pharmacotherapy for opioid use disorder
4. Perioperative uses of intravenous opioids in adults
5. オピオイド中毒治療中の医師監督下の離脱 medically supervised opioid withdrawal during treatment for addiction

English Journal

The action of kisspeptin-13 on passive avoidance learning in mice. Involvement of transmitters.

Telegdy G, Adamik A.SourceDepartment of Pathophysiology, Faculty of Medicine, University of Szeged, Szeged, Hungary; Neuroscience Research Group of the Hungarian Academy of Sciences, Faculty of Medicine, University of Szeged, Szeged, Hungary. Electronic address: telegdy@patph.szote.u-szeged.hu.
Behavioural brain research.Behav Brain Res.2013 Apr 15;243:300-5. doi: 10.1016/j.bbr.2013.01.016. Epub 2013 Jan 21.
Kisspeptins are G protein-coupled receptor ligands originally identified as human metastasis suppressor gene products that have the ability to suppress melanoma and breast cancer metastasis and recently found to play an important role in initiating the secretion of gonadotropin-releasing hormone at
PMID 23348107

Cancer Pain Management: What's New?

Gaertner J, Schiessl C.SourceDepartment of Palliative Care, University Hospital Cologne, 50924, Cologne, Germany, jan.gaertner@uk-koeln.de.
Current pain and headache reports.Curr Pain Headache Rep.2013 Apr;17(4):328. doi: 10.1007/s11916-013-0328-9.
Decades after the publication of the World Health Organization's analgesic ladder, cancer pain is still a major cause of suffering for patients with cancer and affects millions of people worldwide. Owing to the increasing incidence of cancer, cancer-related pain is a major public health problem worl
PMID 23456796

Japanese Journal

ナロキソン (特集拮抗作用から見た麻酔関連薬物の最新知見)

瀬戸口大典,垣花泰之
麻酔 62(1), 5-9, 2013-01
NAID 40019551511

緒言とまとめ (特集拮抗作用から見た麻酔関連薬物の最新知見)

稲田英一
麻酔 62(1), 2-4, 2013-01
NAID 40019551498

Related Pictures

★リンクテーブル★

リンク元	「オピオイド」「麻薬性鎮痛薬」「ナロキソン」
拡張検索	「naloxone hydrochloride」

「オピオイド」

Naloxone
Clinical data
Trade names	Narcan, Evzio, others
Synonyms	EN-1530; N-Allylnoroxymorphone; 17-Allyl-4,5α-epoxy-3,14-dihydroxymorphinan-6-one
AHFS/Drugs.com	Monograph
License data	EU EMA: by INN;
Pregnancy; category	AU: B1 ; US: C (Risk not ruled out) ; ;
Routes of; administration	Endotracheal, intranasal, IV, IM
ATC code	A06AH04 (WHO) ; V03AB15 (WHO);
Legal status
Legal status	AU: S3 (Pharmacist only) ; DE: § 48 AMG/§ 1 MPAV (Prescription only) ; UK: POM (Prescription only) ; US: ℞-only ;
Pharmacokinetic data
Bioavailability	2% (by mouth, 90% absorption but high first-pass metabolism)
Metabolism	Liver
Onset of action	2 min (IV), 5 min (IM)
Elimination half-life	1–1.5 h
Duration of action	30–60 min
Excretion	Urine, bile
Identifiers
	IUPAC name (4R,4aS,7aR,12bS)-4a,9-dihydroxy-3-prop-2-enyl-2,4,5,6,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7-one;
CAS Number	465-65-6 ;
PubChem CID	5284596;
IUPHAR/BPS	1638;
DrugBank	DB01183 ;
ChemSpider	4447644 ;
UNII	36B82AMQ7N;
KEGG	D08249 ;
ChEBI	CHEBI:7459 ;
ChEMBL	CHEMBL80 ;
ECHA InfoCard	100.006.697
Chemical and physical data
Formula	C19H21NO4
Molar mass	327.38 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O=C1[C@@H]2OC3=C(O)C=CC4=C3[C@@]2([C@]5(CC1)O)CCN(CC=C)[C@@H]5C4;
	InChI InChI=1S/C19H21NO4/c1-2-8-20-9-7-18-15-11-3-4-12(21)16(15)24-17(18)13(22)5-6-19(18,23)14(20)10-11/h2-4,14,17,21,23H,1,5-10H2/t14-,17+,18+,19-/m1/s1 ; Key:UZHSEJADLWPNLE-GRGSLBFTSA-N ;
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　　[★]

英: opioid
同: 類麻薬
関: オピオイド受容体

オピオイド受容体に結合するモルフィン様物質のことを指す。

内因性のオピオイドペプチドが発見され、これらは内因性オピオイドペプチドと呼ばれるようになった。

作用

縮瞳

モルフィンと多くのμ,κアゴニストは瞳孔の縮小を引き起こす。これは瞳孔を支配する副交感神経の興奮による。μアゴニストを中毒量投与すると縮瞳し、pinpoints pupupilsはpathognomonicである。(GOO.559)