Information about Reserpine

Reserpine is an indole alkaloid[2] antipsychotic and antihypertensive drug that has been used for the control of high blood pressure and for the relief of psychotic behaviors, although because of the development of better drugs for these purposes and because of its numerous side-effects, it is rarely used today.[7] Reserpine is known to irreversibly bind to storage vesicles of neurotransmitters such as dopamine, norepinephrine, and serotonin.[3] Reserpine depletion of monoamine neurotransmitters in the synapses is often cited as evidence to the theory that depletion of the neurotransmitters causes subsequent depression in humans. Moreover, reserpine has a peripheral action in many parts of the body, resulting in a preponderance of the cholinergic part of the nervous system (GI-Tract, smooth muscles vessels).

History

Reserpine was isolated in 1952 from the dried root of Rauwolfia serpentina (Indian snakeroot),[4] (which had been known as Sarpaganda and had been used for centuries there for the treatment of insanity, as well as fever and snakebites[8]) and introduced it in 1954, two years after chlorpromazine.[5] Reserpine almost irreversibly blocks the uptake (and storage) of norepinephrine (i.e. noradrenaline) and dopamine into synaptic vesicles by inhibiting the Vesicular Monoamine Transporters (VMAT).[6]

Reserpine has been discontinued in the UK for some years due to its vast interactions and side effects.

Reserpine was also highly influential in promoting the thought of a biogenic-amine hypothesis of depression - see Everett & Tolman, 1959.

Uses today

Reserpine is one of the few antihypertensive medications that have been shown in randomized controlled trials to reduce mortality: The Hypertension Detection and Follow-up Program,[9] the Veterans Administration Cooperative Study Group in Anti-hypertensive Agents,[10] and the Systolic Hypertension n the Elderly Program.[11]

Reserpine is listed as a second line choice by the JNC 7.[12] Reserpine is an excellent second agent for patients who are uncontrolled on a diuretic.[13]

In some countries reserpine is still available as part of combination drugs for the treatment of hypertension, in most cases they contain also a diuretic and/or a vasodilator like hydralazine. These combinations are currently regarded as second choice drugs. The daily dose of reserpine in antihypertensive treatment is as low as 0.1 to 0.25mg. The use of reserpine as an antipsychotic drug has been nearly completely abandoned. Originally, doses of 0.5mg to 40mg daily were used to treat psychotic diseases. Doses in excess of 3mg daily often required use of an anticholinergic drug to combat excessive cholinergic activity in many parts of the body as well as parkinsonism. Reserpine may be used as a sedative for horses.

Side effects

At doses of less than 0.2 mg/day, reserpine has few side effects, most commonly is nasal congestion.[14]

There has been much concern about reserpine causing depression leading to suicide. However, this was reported in uncontrolled studies using doses averaging 0.5 mg per day.[15][16]

Reserpine can cause: nasal congestion, nausea, vomiting, weight gain, gastric intolerance, gastric ulceration (due to increased cholinergic activity in gastric tissue and impaired mucosal quality), stomach cramps and diarrhea are noted. The drug causes hypotension and bradycardia and may worsen asthma. Congested nose and erectile dysfunction are other consequences of alpha-blockade. Depression can occur at any dose and may be severe enough to lead to suicide. Other central effects are a high incidence of drowsiness, dizziness, and nightmares. Parkinsonism occurs in a dose dependent manner. General weakness or fatigue is quite often encountered. High dose studies in rodents found reserpine to cause fibroadenoma of the breast and malignant tumors of the semen vesicles among others. Early suggestions that reserpine causes breast cancer in women (risk approximately doubled) were not confirmed.

References

7. ^ [1] The Columbia Encyclopedia, Sixth Edition. Copyright © 2001-05 Columbia University Press.
8. ^ Op. cit. Columbia Encyclopedia
9. ^ (1979) "Five-year findings of the hypertension detection and follow-up program. I. Reduction in mortality of persons with high blood pressure, including mild hypertension. Hypertension Detection and Follow-up Program Cooperative Group". JAMA 242 (23): 2562-71. PMID 490882.  full text at OVID
10. ^ (1967) "Effects of treatment on morbidity in hypertension. Results in patients with diastolic blood pressures averaging 115 through 129 mm Hg". JAMA 202 (11): 1028-34. PMID 4862069. 
11. ^ (1991) "Prevention of stroke by antihypertensive drug treatment in older persons with isolated systolic hypertension. Final results of the Systolic Hypertension in the Elderly Program (SHEP). SHEP Cooperative Research Group". JAMA 265 (24): 3255-64. PMID 2046107. 
12. ^ Chobanian AV, Bakris GL, Black HR, et al (2003). "The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report". JAMA 289 (19): 2560-72. DOI:10.1001/jama.289.19.2560. PMID 12748199.  summary
13. ^ Moser M (1987). ""Cost containment" in the management of hypertension". Ann. Intern. Med. 107 (1): 107-9. PMID 3592424. 
14. ^ Curb JD, Schneider K, Taylor JO, Maxwell M, Shulman N (1988). "Antihypertensive drug side effects in the Hypertension Detection and Follow-up Program". Hypertension 11 (3 Pt 2): II51-5. PMID 3350594. 
15. ^ QUETSCH RM, ACHOR RW, LITIN EM, FAUCETT RL (1959). "Depressive reactions in hypertensive patients; a comparison of those treated with Rauwolfia and those receiving no specific antihypertensive treatment". Circulation 19 (3): 366-75. PMID 13629798. 
16. ^ LEMIEUX G, DAVIGNON A, GENEST J (1956). "Depressive states during Rauwolfia therapy for arterial hypertension; a report of 30 cases". Canadian Medical Association journal 74 (7): 522-6. PMID 13304797. 
  1. ^  アルカロイド (Alkaloids) (T-Z). 2004.
  2. ^  "Indole Alkaloids" Major Types Of Chemical Compounds In Plants & Animals Part II: Phenolic Compounds, Glycosides & Alkaloids. Wayne's Word: An On-Line Textbook of Natural History. 2005.
  3. ^  Forney, Barbara. Reserpine for Veterinary Use Wedgewood Pharmacy. 2001-2002.
  4. ^  Rauwolfia Dorlands Medical Dictionary. Merck Source. 2002.
  5. ^  Lopez-Munoz F, Bhatara VS, Alamo C, Cuenca E. (2004): "[Historical approach to reserpine discovery and its introduction in psychiatry]" [Article in Spanish] Actas Esp Psiquiatr. 32(6):387-95. PMID 15529229 Fulltext in English and Spanish
  6. ^ Schuldiner, S. et al. (1993): J. Biol. Chem. 268(1) 29-34. PMID 8416935

External links

Indole is an aromatic heterocyclic organic compound. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
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alkaloid is, strictly speaking, a naturally occurring amine produced by a plant, but amines produced by animals and fungi are also called alkaloids[1]. Many alkaloids have pharmacological effects on humans and other animals.
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The term antipsychotic is applied to a group of drugs used to treat psychosis. Common conditions with which antipsychotics might be used include schizophrenia, mania and delusional disorder.
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Antihypertensives are a class of drugs that are used in medicine and pharmacology to treat hypertension (high blood pressure). There are many classes of antihypertensives, which—by varying means—act by lowering blood pressure.
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Hypertension
Classification & external resources

ICD-10 I 10. ,I 11. ,I 12. ,
I 13. ,I 15.
ICD-9 401.x

OMIM 145500
DiseasesDB 6330
MedlinePlus 000468
eMedicine med/1106   ped/1097 emerg/267


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Psychosis
Classification & external resources

ICD-9 290 - 299

OMIM 603342 608923 603175 192430

MedlinePlus 001553

MeSH F03.700.
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synaptic vesicles, also called neurotransmitter vesicles, store the various neurotransmitters that are released during calcium-regulated exocytosis at the presynaptic terminal into the synaptic cleft of a synapse.
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Neurotransmitters are chemicals that are used to relay, amplify and modulate signals between a neuron and another cell. According to the prevailing beliefs of the 1960s, a chemical can be classified as a neurotransmitter if it meets the following conditions:

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Dopamine is a hormone and neurotransmitter occurring in a wide variety of animals, including both vertebrates and invertebrates. In chemical structure, it is a phenethylamine.
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Norepinephrine (INN)(abbr. norepi or NE) or noradrenaline (BAN) is a catecholamine and a phenethylamine with chemical formula C8H11NO3. The natural stereoisomer is L -(−)-(R)-norepinephrine.
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Serotonin (pronounced IPA: /ˌsɛrəˈtoʊnən/) (5-hydroxytryptamine, or 5-HT) is a monoamine neurotransmitter synthesized in serotonergic neurons in the central nervous system (CNS) and
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Depression
Classification & external resources

ICD-10 F 32. , F 33.
ICD-9 296

OMIM 608516
DiseasesDB 3589
MedlinePlus 003213
eMedicine med/532  

Clinical depression (also called major-depressive disorder, or
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Rauwolfia
Ruiz & Pav.

Species

About 85 species known.

Rauwolfia (also spelled Rauvolfia) is a genus of evergreen trees and shrubs in the Apocynaceae family.
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Ageratina

Species

many, see text

Snakeroot (Ageratina) is a genus of about 290 annual herbs and rounded shrubs from the Sunflower family (Asteraceae).

These plants grow mainly in the warmer regions of America.
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Chlorpromazine (as chlorpromazine hydrochloride, abbreviated CPZ) is a phenothiazine antipsychotic.

Its principal use is in the treatment of schizophrenia, though it has also been used to treat hiccups and nausea.
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Norepinephrine (INN)(abbr. norepi or NE) or noradrenaline (BAN) is a catecholamine and a phenethylamine with chemical formula C8H11NO3. The natural stereoisomer is L -(−)-(R)-norepinephrine.
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Norepinephrine (INN)(abbr. norepi or NE) or noradrenaline (BAN) is a catecholamine and a phenethylamine with chemical formula C8H11NO3. The natural stereoisomer is L -(−)-(R)-norepinephrine.
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Dopamine is a hormone and neurotransmitter occurring in a wide variety of animals, including both vertebrates and invertebrates. In chemical structure, it is a phenethylamine.
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A randomized controlled trial (RCT) is a scientific procedure most commonly used in testing medicines or medical procedures. RCTs are considered the most reliable form of scientific evidence because it eliminates all forms of spurious causality.
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digital object identifier (or DOI) is a permanent identifier given to a document, which is not related to its current location. A typical use of a DOI is to give a scientific paper or article a unique identifying number that can be used by anyone to locate details of the paper, and
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Antihypertensives are a class of drugs that are used in medicine and pharmacology to treat hypertension (high blood pressure). There are many classes of antihypertensives, which—by varying means—act by lowering blood pressure.
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A section of the Anatomical Therapeutic Chemical Classification System.

C Cardiovascular system

C02A Antiadrenergic agents, centrally acting

C02AA Rauwolfia alkaloids

C02AA01 Rescinnamine
C02AA02 Reserpine

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diuretic is any drug that elevates the rate of bodily stool excretion (diuresis). There are several categories of diuretics. All diuretics increase the excretion of waste from the body, although each class of diuretic does so in a distinct way.
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A section of the Anatomical Therapeutic Chemical Classification System.

C Cardiovascular system

C03A Low-ceiling diuretics, thiazides

C03AA Thiazides, plain

C03AA01 Bendroflumethiazide
C03AA02 Hydroflumethiazide

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An Adrenergic antagonist is a pharmaceutical substance that acts to inhibit the action of the adrenergic receptors.

It has the opposite effect as adrenergic agonists.
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Alpha blockers (also called alpha-adrenergic blocking agents) constitute a variety of drugs which block α1-adrenergic receptors in arteries and smooth muscles.
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Clonidine is a direct-acting adrenergic agonist prescribed historically as an anti-hypertensive agent. It has found new uses, including treatment of some types of neuropathic pain, opioid detoxification, sleep hyperhydrosis, and, off-label, to counter the side effects of stimulant
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Guanfacine (brand name Tenex, and the extended release Intuniv) is a centrally acting antihypertensive agent. Guanfacine lowers both systolic and diastolic blood pressure by activating the central nervous system α-2 adrenergic receptors, which results in reduced
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Methyldopa or alpha-methyldopa (brand names Aldomet®, Apo-Methyldopa®, Dopamet®, Novomedopa®) is a centrally-acting adrenergic antihypertensive medication. Its use is now deprecated following introduction of alternative safer classes of agents.
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Moxonidine (INN) (IPA: [mɒkˈsɒnɪdin]) is a new generation centrally acting antihypertensive drug licensed for the treatment of mild to moderate essential hypertension.
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