Page last updated: 2024-10-28

haloperidol and Insulin Resistance

haloperidol has been researched along with Insulin Resistance in 9 studies

Haloperidol: A phenyl-piperidinyl-butyrophenone that is used primarily to treat SCHIZOPHRENIA and other PSYCHOSES. It is also used in schizoaffective disorder, DELUSIONAL DISORDERS, ballism, and TOURETTE SYNDROME (a drug of choice) and occasionally as adjunctive therapy in INTELLECTUAL DISABILITY and the chorea of HUNTINGTON DISEASE. It is a potent antiemetic and is used in the treatment of intractable HICCUPS. (From AMA Drug Evaluations Annual, 1994, p279)
haloperidol : A compound composed of a central piperidine structure with hydroxy and p-chlorophenyl substituents at position 4 and an N-linked p-fluorobutyrophenone moiety.

Insulin Resistance: Diminished effectiveness of INSULIN in lowering blood sugar levels: requiring the use of 200 units or more of insulin per day to prevent HYPERGLYCEMIA or KETOSIS.

Research Excerpts

ExcerptRelevanceReference
"The aim of this study was to compare serum amino acid patterns in patients on long-term clozapine treatment with long-term conventional antipsychotic treatment, and their relationships to insulin resistance and antipsychotic serum concentrations."7.81Higher serum concentrations of tyrosine and glutamate in schizophrenia patients treated with clozapine, compared to in those treated with conventional antipsychotics. ( Hall, K; Lewitt, M; Melkersson, K, 2015)
"The aim of this study was to compare serum amino acid patterns in patients on long-term clozapine treatment with long-term conventional antipsychotic treatment, and their relationships to insulin resistance and antipsychotic serum concentrations."3.81Higher serum concentrations of tyrosine and glutamate in schizophrenia patients treated with clozapine, compared to in those treated with conventional antipsychotics. ( Hall, K; Lewitt, M; Melkersson, K, 2015)
" To investigate the possible mechanisms of antipsychotic-induced metabolic effects, we studied the impact of chronic administration of a typical antipsychotic drug (haloperidol) and an atypical antipsychotic (risperidone) to male rats on food intake, body weight, adiposity, and the circulating concentrations of hormones and metabolites that can influence energy homeostasis."3.73Distinct endocrine effects of chronic haloperidol or risperidone administration in male rats. ( Dedova, I; Duffy, L; Herzog, H; Karl, T; Lee, NJ; Lin, EJ; Matsumoto, I; O'brien, E; Sainsbury, A; Slack, K, 2006)
"Weight gain was positively correlated with changes in insulin levels, insulin resistance index and triglyceride levels."2.74Glucose and lipid disturbances after 1 year of antipsychotic treatment in a drug-naïve population. ( Amado, JA; Berja, A; Crespo-Facorro, B; Garcia-Unzueta, MT; Martinez-Garcia, O; Mata, I; Pelayo-Teran, JM; Perez-Iglesias, R; Vazquez-Barquero, JL, 2009)
"Haloperidol treatment reduced the voluntary activity and energy expenditure of DR mice and induced insulin resistance in these mice."1.37Pharmacological modulation of dopamine receptor D2-mediated transmission alters the metabolic phenotype of diet induced obese and diet resistant C57Bl6 mice. ( de Leeuw van Weenen, JE; Parlevliet, ET; Pijl, H; Romijn, JA; Schröder-van der Elst, JP; van den Berg, SA; Willems van Dijk, K, 2011)

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (22.22)29.6817
2010's7 (77.78)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Calevro, A1
Cotel, MC1
Natesan, S1
Modo, M1
Vernon, AC1
Mondelli, V1
Melkersson, K1
Lewitt, M1
Hall, K1
Perez-Iglesias, R1
Mata, I1
Pelayo-Teran, JM1
Amado, JA1
Garcia-Unzueta, MT1
Berja, A1
Martinez-Garcia, O1
Vazquez-Barquero, JL1
Crespo-Facorro, B1
Boyda, HN1
Tse, L1
Procyshyn, RM1
Wong, D1
Wu, TK1
Pang, CC1
Barr, AM1
Albaugh, VL1
Vary, TC1
Ilkayeva, O1
Wenner, BR1
Maresca, KP1
Joyal, JL1
Breazeale, S1
Elich, TD1
Lang, CH1
Lynch, CJ1
Victoriano, M1
de Beaurepaire, R1
Naour, N1
Guerre-Millo, M1
Quignard-Boulangé, A1
Huneau, JF1
Mathé, V1
Tomé, D1
Hermier, D1
de Leeuw van Weenen, JE2
Auvinen, HE1
Parlevliet, ET2
Coomans, CP1
Schröder-van der Elst, JP2
Meijer, OC1
Pijl, H2
van den Berg, SA1
Willems van Dijk, K1
Romijn, JA1
Lin, EJ1
Lee, NJ1
Slack, K1
Karl, T1
Duffy, L1
O'brien, E1
Matsumoto, I1
Dedova, I1
Herzog, H1
Sainsbury, A1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Double-blind, Placebo-controlled, Crossover Study Examining the Acute Effects of Olanzapine on Plasma Leptin, Glucose Tolerance and Free Fatty Acids in Healthy Volunteers[NCT00741026]15 participants (Actual)Interventional2008-08-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

BMI

BMI (NCT00741026)
Timeframe: 3 Days

Interventionkg / m2 (Mean)
Placebo23.0
Olanzapine23.0

Body Weight

Body Weight (NCT00741026)
Timeframe: 3 Days

Interventionkg (Mean)
Placebo68.2
Olanzapine68.9

Diastolic Blood Pressure

Diastolic Blood Pressure (NCT00741026)
Timeframe: 3 Days

InterventionmmHg (Mean)
Placebo68.3
Olanzapine69.5

HDL Cholesterol

HDL Cholesterol (NCT00741026)
Timeframe: 3 Days

Interventionmg/dl (Mean)
Placebo54.2
Olanzapine48.9

Heart Rate

Heart Rate (NCT00741026)
Timeframe: 3 Days

Interventionbeats per minute (Mean)
Placebo69.9
Olanzapine67.6

LDL Cholesterol

LDL Cholesterol (NCT00741026)
Timeframe: 3 Days

Interventionmg/dl (Mean)
Placebo82.7
Olanzapine81.7

Oral Glucose Tolerance

Oral Glucose Tolerance (NCT00741026)
Timeframe: 3 Days

Interventionmin*mg/dl (Mean)
Placebo2808
Olanzapine3984

Plasma Free Fatty Acid

Plasma Free Fatty Acid (NCT00741026)
Timeframe: 3 Days

InterventionmM (Mean)
Placebo0.38
Olanzapine0.26

Plasma Leptin

Leptin following placebo or olanzapine treatment (NCT00741026)
Timeframe: 3 Days

Interventionng/ml (Mean)
Placebo6.8
Olanzapine8.4

Systolic Blood Pressure

Systolic Blood Pressure (NCT00741026)
Timeframe: 3 Days

InterventionmmHg (Mean)
Placebo113.3
Olanzapine111.7

Total Cholesterol

Total Cholesterol (NCT00741026)
Timeframe: 3 Days

Interventionmg/dl (Mean)
Placebo156.8
Olanzapine152.6

Triglycerides

Triglycerides (NCT00741026)
Timeframe: 3 Days

Interventionmg/dl (Mean)
Placebo88.9
Olanzapine108.2

Trials

1 trial available for haloperidol and Insulin Resistance

ArticleYear
Glucose and lipid disturbances after 1 year of antipsychotic treatment in a drug-naïve population.
    Schizophrenia research, 2009, Volume: 107, Issue:2-3

    Topics: Adolescent; Adult; Antipsychotic Agents; Benzodiazepines; Blood Glucose; Cholesterol; Cholesterol, H

2009

Other Studies

8 other studies available for haloperidol and Insulin Resistance

ArticleYear
Effects of chronic antipsychotic drug exposure on the expression of Translocator Protein and inflammatory markers in rat adipose tissue.
    Psychoneuroendocrinology, 2018, Volume: 95

    Topics: Adipose Tissue; Adiposity; Animals; Antigens, Differentiation; Antipsychotic Agents; Biomarkers; Car

2018
Higher serum concentrations of tyrosine and glutamate in schizophrenia patients treated with clozapine, compared to in those treated with conventional antipsychotics.
    Neuro endocrinology letters, 2015, Volume: 36, Issue:5

    Topics: Adult; Amino Acids; Antipsychotic Agents; Chromatography, Ion Exchange; Clopenthixol; Clozapine; Coh

2015
A parametric study of the acute effects of antipsychotic drugs on glucose sensitivity in an animal model.
    Progress in neuro-psychopharmacology & biological psychiatry, 2010, Aug-16, Volume: 34, Issue:6

    Topics: Analysis of Variance; Animals; Antipsychotic Agents; Blood Glucose; Clozapine; Dose-Response Relatio

2010
Atypical antipsychotics rapidly and inappropriately switch peripheral fuel utilization to lipids, impairing metabolic flexibility in rodents.
    Schizophrenia bulletin, 2012, Volume: 38, Issue:1

    Topics: Animals; Antipsychotic Agents; Benzodiazepines; Carnitine; Clozapine; Energy Metabolism; Fatty Acids

2012
Olanzapine-induced accumulation of adipose tissue is associated with an inflammatory state.
    Brain research, 2010, Sep-02, Volume: 1350

    Topics: Adipose Tissue; Analysis of Variance; Animals; Antipsychotic Agents; Benzodiazepines; Cytokines; Glu

2010
Blocking dopamine D2 receptors by haloperidol curtails the beneficial impact of calorie restriction on the metabolic phenotype of high-fat diet induced obese mice.
    Journal of neuroendocrinology, 2011, Volume: 23, Issue:2

    Topics: Animals; Body Weight; Caloric Restriction; Dietary Fats; Dopamine Antagonists; Dopamine D2 Receptor

2011
Pharmacological modulation of dopamine receptor D2-mediated transmission alters the metabolic phenotype of diet induced obese and diet resistant C57Bl6 mice.
    Experimental diabetes research, 2011, Volume: 2011

    Topics: Animals; Behavior, Animal; Body Weight; Bromocriptine; Dietary Fats; Dopamine Agonists; Dopamine Ant

2011
Distinct endocrine effects of chronic haloperidol or risperidone administration in male rats.
    Neuropharmacology, 2006, Volume: 51, Issue:7-8

    Topics: Adipose Tissue; Animals; Antipsychotic Agents; Appetite; Body Weight; Corticosterone; Diabetes Melli

2006