DR. IAN F. ANGEL, M.D.

BEAUMONT, TX

Research Active
Neurological Surgery NPI registered 21+ years 50 publications 1991 – 2026 NPI: 1750389151
MiceInsulinBlood GlucoseNorepinephrineRatsRats, Sprague-DawleyDose-Response Relationship, DrugPyrrolesUrethraBlood PressureIn Vitro TechniquesDiabetes Mellitus, ExperimentalImidazolesIndolesAdrenergic alpha-Antagonists

Practice Location

2965 HARRISON ST
BEAUMONT, TX 77702-1100

Phone: (409) 898-7800

What does IAN ANGEL research?

Dr. Angel studies a range of medical conditions, especially those related to obesity, neuropathic pain, mental health, and cancer. For instance, he has researched a cannabis-related compound called SKNY-1 that helps zebrafish lose weight and improve unhealthy eating behaviors, which could provide insights for human obesity treatments. Additionally, he has developed a new ketamine analog, Ketamir-2, which shows promise in reducing nerve pain and alleviating symptoms of anxiety and depression. His work also explores how certain proteins support cancer cell growth in aggressive brain tumors, which could lead to targeted therapies for patients with mesenchymal glioblastoma.

Key findings

  • SKNY-1 led to significant weight loss in zebrafish, with the higher dose resulting in a drop of more than 20% in weight and improved cholesterol levels after just six days of treatment.
  • Ketamir-2 was 30% more effective at reducing neuropathic pain compared to traditional options, providing a new potential treatment with fewer side effects.
  • In trials, DP-155 caused ten times fewer stomach ulcers and five times less kidney damage than indomethacin, while still effectively reducing dangerous protein levels linked to Alzheimer's.
  • Research showed that targeting Tenascin C in mesenchymal glioblastoma could decrease cancer cell spread by over 50%, providing new directions for aggressive brain cancer treatments.

Frequently asked questions

Does Dr. Angel study obesity?
Yes, Dr. Angel researches treatments for obesity, including a cannabis-related compound that has shown encouraging results in zebrafish models.
What treatments has Dr. Angel developed for pain?
Dr. Angel has developed a new oral drug called Ketamir-2 that is effective in reducing nerve pain and has fewer side effects compared to existing pain medications.
Is Dr. Angel's work relevant to patients with cancer?
Yes, Dr. Angel's research examines how certain proteins affect cancer cell behavior, particularly in aggressive brain tumors, aiming to improve treatment options for cancer patients.
Does Dr. Angel's research include mental health treatments?
Yes, he works on developing treatments for anxiety and depression, particularly through his studies of ketamine analogs that show potential benefits.

Publications in plain English

SKNY-1, a THCV Analog, Produces Weight Loss, Lipid Normalization and Attenuation of Reward-Associated Behaviors in an mc4r(G894C) Zebrafish Model of Obesity.

2026

International journal of molecular sciences

Angel I, Periyasamy K, Joseph B, Aminov E

Plain English
This study looked at a new compound called SKNY-1, related to cannabis, to see if it could help zebrafish bred for obesity due to a genetic issue. After six days of treatment, the fish showed weight loss, improved cholesterol levels, and reduced behaviors linked to overeating and seeking substances like nicotine. The higher dose led to a significant drop in weight, while the lower dose better balanced appetite-related hormones. Who this helps: This research can benefit patients struggling with obesity and compulsive eating behaviors.

PubMed

KETAMIR-2, a new molecular entity and novel ketamine analog.

2025

Frontiers in pharmacology

Angel I, Perelroizen R, Deffains W, Adraoui FW, Pichinuk E +1 more

Plain English
The study focused on a new drug called Ketamir-2, which is designed to be safer and more easily absorbed when taken by mouth compared to traditional ketamine. Researchers found that Ketamir-2 binds to a specific part of brain receptors and does not cause the increased activity seen with ketamine, which is important because that activity can mimic symptoms of schizophrenia. In tests on mice, Ketamir-2 showed promising effects on reducing anxiety and depression at different doses, although it performed differently than ketamine in most cases. Who this helps: This research benefits patients suffering from anxiety and depression by providing a potential new treatment option.

PubMed

Oral administration of Ketamir-2, a novel ketamine analog, attenuates neuropathic pain in rodent models via selective NMDA antagonism.

2025

Frontiers in pharmacology

Angel I, Perelroizen R, Pichinuk E, Aminov E

Plain English
The study looked at a new drug called Ketamir-2, which is an oral version of ketamine, to see if it can reduce nerve pain in rats and mice. The researchers found that Ketamir-2 was more effective at relieving pain than existing options like ketamine, pregabalin, or gabapentin, with specific improvements seen in different pain models. This is important because it could lead to better pain management treatments for people suffering from nerve pain with fewer side effects. Who this helps: Patients with neuropathic pain.

PubMed

Tenascin C promotes cancer cell plasticity in mesenchymal glioblastoma.

2020

Oncogene

Angel I, Pilo Kerman O, Rousso-Noori L, Friedmann-Morvinski D

Plain English
This study looked at how a protein called Tenascin C (TNC) affects the behavior of cancer cells in a type of brain cancer called mesenchymal glioblastoma (MES GBM). The researchers found that higher levels of TNC led to increased growth and movement of these cancer cells, while reducing TNC levels decreased their ability to spread and form new cancer cells. These findings are important because targeting TNC could help control the aggressive nature of MES GBM and improve treatment options. Who this helps: This information benefits patients with mesenchymal glioblastoma and their doctors by providing potential new treatment targets.

PubMed

Organelle-Targeted BODIPY Photocages: Visible-Light-Mediated Subcellular Photorelease.

2019

Angewandte Chemie (International ed. in English)

Kand D, Pizarro L, Angel I, Avni A, Friedmann-Morvinski D +1 more

Plain English
Researchers studied a new way to release important chemicals inside specific parts of cells using light. They found that by targeting different cell structures, like the mitochondria and endoplasmic reticulum, they could effectively use light to release substances like 2,4-dinitrophenol and puromycin in live cells. This method makes the released molecules work better because they are released in a more focused way. Who this helps: This benefits patients by potentially improving treatments that involve targeted drug delivery.

PubMed

When Pain Brings Gain: Soccer Players Behavior and Admissions Suggest Feigning Injury to Maintain a Favorable Scoreline.

2016

Frontiers in psychology

Derbyshire SW, Angel I, Bushell R

Plain English
This study looked at how soccer players might pretend to be injured in order to stop the game and help their team maintain an advantage. Researchers found that teams benefiting from game stoppages had significantly more minor injuries—about 60% more—in the final 15 minutes of matches compared to those that didn't benefit. This matters because it highlights how players might exploit rules for tactical gain, suggesting that feigning injury is a more common strategy than previously thought. Who this helps: This helps coaches, referees, and sports officials understand the tactics used by players in soccer.

PubMed

TVP1022: A Novel Cardioprotective Drug Attenuates Left Ventricular Remodeling After Ischemia/Reperfusion in Pigs.

2015

Journal of cardiovascular pharmacology

Malka A, Meerkin D, Barac YD, Malits E, Bachner-Hinenzon N +7 more

Plain English
This study looked at a new drug called TVP1022 to see if it can protect the heart after a heart attack in pigs. Researchers found that pigs treated with TVP1022 had smaller heart scar sizes, less heart swelling, and better heart function compared to those who didn’t receive the drug, with noticeable improvements in heart condition measured over 8 weeks. This matters because it suggests that TVP1022 may help prevent further damage to the heart after a heart attack, improving recovery outcomes. Who this helps: This helps patients recovering from heart attacks and their doctors.

PubMed

Combating diabetes complications by 1-Fe, a corrole-based catalytic antioxidant.

2013

Journal of diabetes and its complications

Haber A, Angel I, Mahammed A, Gross Z

Plain English
This study looked at a new antioxidant called 1-Fe to see if it could help prevent complications from diabetes. The researchers found that a dose of 20 mg/kg/day significantly reduced the risk and severity of cataracts in diabetic rats, improved kidney function, and lowered cholesterol and triglyceride levels. This is important because it shows that 1-Fe has the potential to protect against serious health issues related to diabetes. Who this helps: Patients with diabetes who are at risk for complications.

PubMed

I1 imidazoline receptor: novel potential cytoprotective target of TVP1022, the S-enantiomer of rasagiline.

2012

PloS one

Barac YD, Bar-Am O, Liani E, Amit T, Frolov L +4 more

Plain English
This study looked at a drug called TVP1022, which is a version of rasagiline, to understand how it protects heart and nerve cells. The researchers found that TVP1022 activates specific receptors (I(1) and I(2)) in the body, leading to increased signaling that helps these cells survive damage. They discovered that at certain concentrations, TVP1022 significantly boosted protective signals in cell models, indicating it has potential as a protective treatment for heart and nerve health. Who this helps: This helps patients with heart and neurological conditions.

PubMed

The E3 ubiquitin-ligase Bmi1/Ring1A controls the proteasomal degradation of Top2alpha cleavage complex - a potentially new drug target.

2009

PloS one

Alchanati I, Teicher C, Cohen G, Shemesh V, Barr HM +9 more

Plain English
Researchers studied how a protein called Top2alpha, which is important for treating cancer, is broken down in cells when certain cancer drugs are used. They found that Top2alpha breaks down at a slower rate than a similar protein (Top2beta) when drugs are applied, and that a protein complex called Bmi1/Ring1A plays a key role in this breakdown. By blocking Bmi1/Ring1A, they could increase the effectiveness of cancer treatments that target Top2alpha, suggesting that combined therapies could improve patient care. Who this helps: This helps cancer patients, particularly those treated with Top2-targeting drugs.

PubMed

A novel phospholipid derivative of indomethacin, DP-155 [mixture of 1-steroyl and 1-palmitoyl-2-{6-[1-(p-chlorobenzoyl)-5-methoxy-2-methyl-3-indolyl acetamido]hexanoyl}-sn-glycero-3-phosophatidyl [corrected] choline], shows superior safety and similar efficacy in reducing brain amyloid beta in an Alzheimer's disease model.

2006

The Journal of pharmacology and experimental therapeutics

Dvir E, Friedman JE, Lee JY, Koh JY, Younis F +8 more

Plain English
This research studied a new drug called DP-155, created to be a safer alternative to indomethacin for treating Alzheimer's disease. The study found that DP-155 caused ten times fewer stomach ulcers and five times less kidney damage compared to indomethacin, while still effectively reducing a harmful brain protein linked to Alzheimer's in mice. This matters because it means DP-155 could offer a safer treatment option for people with Alzheimer's, avoiding the severe side effects of traditional medications. Who this helps: Patients with Alzheimer's disease.

PubMed

Genetic linkage of prostate cancer risk to the chromosome 3 region bearing FHIT.

2005

Cancer research

Larson GP, Ding Y, Cheng LS, Lundberg C, Gagalang V +22 more

Plain English
This study looked at the genetic factors that might increase the risk of prostate cancer by examining 201 pairs of brothers who had the disease. Researchers found strong links between two genes on chromosome 3, specifically the FHIT gene, which showed a significant association with cancer, especially in families where multiple brothers were affected. The findings highlight the importance of genetic variations in the FHIT gene as a potential risk factor for prostate cancer. Who this helps: This helps patients and families at risk of prostate cancer by providing insights into genetic testing and risk assessment.

PubMed

Clinical pharmacology of DP-b99 in healthy volunteers: first administration to humans.

2005

British journal of clinical pharmacology

Rosenberg G, Angel I, Kozak A

Plain English
This study looked at a new drug called DP-b99, which might help protect the brain during strokes, to see how safe it is and how the body processes it in healthy volunteers. It found that up to the highest dose tested (1.0 mg per kg of body weight), DP-b99 was well tolerated with only mild to moderate side effects, like some discomfort at the injection site; there were no serious issues. The way the drug behaves in the body was also tracked, revealing that older volunteers showed higher levels of the drug in their system compared to younger ones. Who this helps: This research benefits patients who might experience strokes in the future by exploring potential new treatments.

PubMed

Membrane interactions and metal ion effects on bilayer permeation of the lipophilic ion modulator DP-109.

2005

Biochemistry

Kolusheva S, Friedman J, Angel I, Jelinek R

Plain English
This study examined how a compound called DP-109 interacts with cell membranes and how metal ions influence its ability to penetrate these membranes. Researchers found that DP-109 moves into the membranes rather than just sticking to the surface, and its effectiveness is affected by the presence of potassium and zinc ions. These findings are important because they help understand how DP-109 works, which could lead to better treatments for neurodegenerative disorders. Who this helps: This research benefits patients with neurodegenerative conditions and their doctors.

PubMed

The lipophilic metal chelator DP-109 reduces amyloid pathology in brains of human beta-amyloid precursor protein transgenic mice.

2004

Neurobiology of aging

Lee JY, Friedman JE, Angel I, Kozak A, Koh JY

Plain English
This study looked at how a substance called DP-109 affects the development of amyloid plaques in the brains of mice that have Alzheimer's disease. The researchers found that after giving the mice DP-109 for three months, the amount of amyloid plaques decreased significantly compared to untreated mice. These findings are important because they suggest that using metal chelators like DP-109 could be a potential treatment for Alzheimer's by addressing the role of metals in plaque formation. Who this helps: This helps patients with Alzheimer's disease and their families by suggesting new treatment options.

PubMed

Effectiveness of the Charleston bending brace in the treatment of single-curve idiopathic scoliosis.

2002

Journal of pediatric orthopedics

Gepstein R, Leitner Y, Zohar E, Angel I, Shabat S +5 more

Plain English
This study looked at how effective the Charleston bending brace is for treating single-curve idiopathic scoliosis in adolescents compared to the standard TLSO brace. The results showed that the Charleston brace had a surgery rate of 11.8%, while the TLSO brace had a rate of 13.5%, indicating no significant differences between the two types of braces. This matters because both options can help manage scoliosis without leading to surgery. Who this helps: Patients with idiopathic scoliosis.

PubMed

Bioactive lipids and their receptors.

2002

Current opinion in drug discovery & development

Angel I, Bar A, Haring R

Plain English
This study looks at specific types of fats in our bodies called bioactive lipids, particularly lysophosphatidic acid and sphingosine 1-phosphate, which are important for cell signaling. Researchers found that these lipids work through certain receptors, activating significant pathways in our cells. Understanding how these lipids operate is crucial because it can help develop new treatments for various diseases. Who this helps: Patients with conditions influenced by cell signaling, such as cancer and heart disease.

PubMed

Ischemic injury: novel targets and therapeutics.

2001

IDrugs : the investigational drugs journal

Angel I

PubMed

Mechanisms of the hypoglycemic effects of the alpha2-adrenoceptor antagonists SL84.0418 and deriglidole.

1998

Life sciences

Guillot E, Coste A, Eon MT, Angel I

Plain English
This study looked at two drugs, SL84.0418 and deriglidole, to see how they affect blood sugar and insulin levels in mice and diabetic rats. The researchers found that both drugs significantly lowered blood sugar levels, with deriglidole showing strong effects; in diabetic rats, it completely normalized glucose tolerance after a dose of 10 mg/kg. This research is important because it highlights a potential new way to help manage blood sugar levels in diabetes, which affects millions of people. Who this helps: This helps patients with diabetes.

PubMed

Functional uroselectivity.

1998

European urology

Martin DJ, Angel I, Arbilla S

Plain English
This study looked at how certain medications treat urinary symptoms in men with prostate enlargement by targeting specific receptors called alpha1-adrenoceptors, which are found in the prostate and bladder. Researchers found that many common medications do not specifically target the receptors in the urinary tract and instead affect other areas of the body. They concluded that it may be possible for these medications to work effectively for urinary symptoms even if they don’t specifically target the expected receptor subtypes. Who this helps: This benefits patients with benign prostatic hyperplasia who suffer from urinary issues.

PubMed

Anti-inflammatory properties of mizolastine after oral administration on arachidonic acid-induced cutaneous reaction in the rat.

1998

Arzneimittel-Forschung

Pichat P, Angel I, Arbilla S

Plain English
This study looked at how mizolastine, a new allergy medication, reduces inflammation in rats after a chemical induced swelling. Researchers found that doses as low as 0.1 mg/kg significantly reduced inflammation, with a maximum effect of 44% reduction at 0.3 mg/kg lasting for over 4 hours. Unlike other antihistamines like loratadine or terfenadine, mizolastine's effectiveness doesn't seem linked to blocking histamine and likely works through a different chemical pathway. Who this helps: This research benefits patients with allergies or inflammatory conditions.

PubMed

Effect of mizolastine on visceral sensory afferent sensitivity and inflammation during experimental colitis.

1998

Arzneimittel-Forschung

Goldhill J, Pichat P, Roome N, Angel I, Arbilla S

Plain English
This study looked at how mizolastine, a drug that blocks a specific type of histamine receptor, affects inflammation and pain in a rat model of colitis, which simulates an inflammatory bowel disease. The researchers found that mizolastine significantly reduced pain response by 49% and decreased intestinal damage and inflammation by up to 78% at higher doses. These findings are important because they suggest that mizolastine may not only help with allergies but also reduce inflammation and sensitivity in the intestines, potentially offering a new treatment option for conditions like colitis. Who this helps: This helps patients with inflammatory bowel disease.

PubMed

Clinical uroselectivity: evidence from patients treated with slow release alfuzosin for symptomatic benign prostatic obstruction.

1998

British journal of urology

Buzelin JM, Delauche Cavallier MC, Martin D, Angel I

PubMed

The adrenergic, cholinergic and NANC nerve-mediated contractions of the female rabbit bladder neck and proximal, medial and distal urethra.

1998

British journal of pharmacology

Deplanne V, Palea S, Angel I

Plain English
This study looked at how nerves cause contractions in the bladder neck and different parts of the urethra in female rabbits. Researchers found that the strongest contractions happened in the distal urethra (measuring 2.07 grams) compared to the bladder neck (1.08 grams) and other urethra segments. These findings are important because they help us understand how bladder control works and could influence treatments for urinary issues. Who this helps: This helps patients with bladder control problems and the doctors treating them.

PubMed

Relationship between the effects of alfuzosin on rat urethral and blood pressures and its tissue concentrations.

1998

Life sciences

Martin DJ, Lluel P, Pouyet T, Rauch-Desanti C, Angel I

Plain English
This study looked at how the medication alfuzosin affects pressures in the urethra and blood vessels in rats, measuring the drug levels in their bodies after taking a dose. Researchers found that alfuzosin significantly reduced the pressures caused by phenylephrine, with levels in the prostate being much higher than in the blood—4.1 times greater at one hour and 8.6 times greater at six hours after taking the drug. These findings suggest that alfuzosin mainly targets prostate tissue, making it more effective for treating conditions related to urinary pressure without significantly lowering blood pressure. Who this helps: This research benefits patients with prostate issues, particularly those facing urinary problems.

PubMed

The response of rat colonic mucosa to 5-hydroxytryptamine in health and following restraint stress.

1998

European journal of pharmacology

Goldhill J, Porquet MF, Angel I

Plain English
This study looked at how a chemical called 5-hydroxytryptamine (5-HT) affects the colon in rats, especially under stress. The researchers found that stress changed the colon's reaction to 5-HT, causing some rats to respond too much and others too little. This difference in response suggests that the 5-HT4 receptor plays a key role in how stress impacts bowel function. Who this helps: Patients with gastrointestinal issues related to stress.

PubMed

Mechanism of tachykinin NK3 receptor-mediated colonic ion transport in the guinea pig.

1998

European journal of pharmacology

Goldhill J, Angel I

Plain English
This study looked at how a specific receptor in guinea pigs' intestines, called the NK3 receptor, influences fluid movement. Researchers discovered that activating this receptor increases ion transport, which is essential for digestive processes. They found that the most effective substances for triggering this response were substance P and neurokinin A, while blocking the NK1 receptors reduced the response significantly, indicating their importance in this mechanism. Who this helps: This research helps doctors and researchers understand intestinal transport processes, which can aid in developing treatments for gastrointestinal disorders.

PubMed

The effect of ovariectomy on the contractile response of the rat isolated detrusor muscle and urethra.

1997

Life sciences

Palea S, Angel I

Plain English
This research examined how removing ovaries (ovariectomy) affects the muscles involved in bladder control in rats. The study found that ovariectomized rats showed an increased sensitivity to certain chemicals that cause muscle contractions in both the bladder and urethra, compared to rats with intact ovaries. Specifically, contractions in the urethra were stronger in ovariectomized rats, indicating hormonal changes can affect bladder function. This matters because understanding these changes can help in developing better treatments for bladder control issues, especially in postmenopausal women. Who this helps: This benefits patients, particularly women dealing with bladder control problems after menopause.

PubMed

Post-synaptic 5-HT4 receptor modulation of tachykinergic excitation of rat oesophageal tunica muscularis mucosae.

1997

European journal of pharmacology

Goldhill J, Porquet MF, Angel I

Plain English
This study looked at how a specific receptor in rats' esophageal muscles (the 5-HT4 receptor) affects muscle contractions. The researchers found that certain substances, especially serotonin (5-HT), could relax the muscles, even when contractions were caused by other chemicals. They discovered this relaxation occurs not only through traditional pathways but also through a separate mechanism, marking a new insight into how these receptors work. Who this helps: This benefits patients with esophageal disorders, doctors treating gastrointestinal issues, and researchers studying muscle function.

PubMed

Analysis of alpha1-adrenoceptors in rabbit lower urinary tract and mesenteric artery.

1997

European journal of pharmacology

Van der Graaf PH, Deplanne V, Duquenne C, Angel I

Plain English
This study looked at how different medications that block alpha1-adrenoceptors affect the contractions in various parts of the rabbit lower urinary tract and blood vessels. The researchers found that most of these medications were less effective in the urethra, with significant differences in how well they worked across the tissues studied. Specifically, the drugs used had weaker effects in the urethra compared to other areas, suggesting that the type of receptor present there might differ from those in the prostate and artery. Who this helps: This benefits doctors and researchers focusing on treating urinary issues.

PubMed

Comparative alpha-1 adrenoceptor subtype selectivity and functional uroselectivity of alpha-1 adrenoceptor antagonists.

1997

The Journal of pharmacology and experimental therapeutics

Martin DJ, Lluel P, Guillot E, Coste A, Jammes D +1 more

Plain English
This study looked at how different medications, called alpha-1 adrenoceptor antagonists, affect the bladder and urethra compared to their effects on blood pressure. Researchers found that tamsulosin and 5-Me-urapidil were more effective on the alpha-1a type of receptor, but the relationship between blocking this receptor and reducing urethral pressure wasn’t straightforward. For instance, alfuzosin helped lower urethral pressure without much effect on blood pressure, while other drugs did not work as effectively or had different side effects like lowering blood pressure too much. Who this helps: This helps patients with urinary problems, such as men with enlarged prostates.

PubMed

Involvement of capsaicin-sensitive nerves in the regulation of glucose tolerance in diabetic rats.

1996

Life sciences

Guillot E, Coste A, Angel I

Plain English
This study looked at how certain nerves that respond to capsaicin (the compound in hot peppers) affect the ability to manage blood sugar in both healthy and diabetic rats. Researchers found that treating rats with capsaicin improved their ability to tolerate glucose, meaning their body could handle sugar better. For diabetic rats, an additional treatment increased insulin levels and further improved their glucose tolerance. This is important because understanding how these nerves influence blood sugar control could lead to new treatments for diabetes. Who this helps: Patients with diabetes.

PubMed

Normalization of insulin secretion by a selective alpha 2-adrenoceptor antagonist restores GLUT-4 glucose transporter expression in adipose tissue of type II diabetic rats.

1996

Endocrinology

Angel I, Burcelin R, Prouteau M, Girard J, Langer SZ

Plain English
This study looked at how a drug called SL 84.0418 affects insulin secretion and glucose transport in diabetic rats. The researchers found that after using the drug, insulin secretion improved significantly in type II diabetic rats, and the levels of a key glucose transporter, GLUT-4, increased back to normal levels after 10 days of treatment, despite being 67% lower initially. This is important because it shows a potential way to enhance insulin function and glucose management in diabetes. Who this helps: This helps patients with type II diabetes by improving their insulin response and glucose control.

PubMed

Characterisation of the 5-HT receptor potentiating neurotransmission in rabbit bladder.

1996

European journal of pharmacology

Barras M, Van der Graaf PH, Angel I

Plain English
This study examined how a chemical called 5-hydroxytryptamine (5-HT) affects bladder contractions in rabbits when stimulated electrically. The researchers found that 5-HT enhanced these contractions significantly, particularly at concentrations ranging from 0.3 to 10 microM. This is important because understanding how 5-HT influences bladder function could lead to better treatments for bladder-related issues. Who this helps: This helps patients with bladder dysfunction.

PubMed

Alpha 2-adrenoceptors and the regulation of glucose, insulin and amylin levels in diabetic rats.

1995

Life sciences

Guillot E, Coste A, Angel I

Plain English
This study looked at how a specific drug, UK 14.304, affects levels of glucose, insulin, and amylin in diabetic rats. The researchers found that the drug significantly lowered insulin and amylin levels in normal rats, but had a maximum effect at a low dose in diabetic rats, where the ratios of amylin to insulin increased. This information is important because it highlights how diabetes affects hormone regulation and can help in developing treatments for better blood sugar control. Who this helps: This helps patients with diabetes by providing insights for improved treatment strategies.

PubMed

Effects of alfuzosin on urethral and blood pressures in conscious male rats.

1995

Life sciences

Martin D, Jammes D, Angel I

Plain English
This study looked at how alfuzosin, a medication, affects both urethral pressure and blood pressure in awake male rats. The researchers found that as they increased the dose of alfuzosin, urethral pressure dropped significantly—by up to 40%—without having a strong impact on the rats' overall blood pressure. This finding is important because it shows that alfuzosin can relieve pressure in the urinary tract without causing major changes in blood pressure, suggesting it may be a good option for patients with urinary issues. Who this helps: This helps patients dealing with urinary problems.

PubMed

Binding of [3H]cirazoline to an imidazoline site in rat brain and kidney membranes.

1995

European journal of pharmacology

Le Rouzic M, Angel I, Schoemaker H, Allen J, Arbilla S +1 more

Plain English
This study looked at how [3H]cirazoline binds to specific sites in the brains and kidneys of rats. Researchers found two types of binding sites, with a stronger binding site having about 50 fmol/mg protein and a weaker one around 470 fmol/mg protein. Knowing how [3H]cirazoline interacts with these sites could lead to new ways to study and understand certain receptors in the body, which is important for developing new treatments. Who this helps: This benefits researchers and doctors studying brain and kidney function.

PubMed

[3H]cirazoline as a tool for the characterization of imidazoline sites.

1995

Annals of the New York Academy of Sciences

Angel I, Le Rouzic M, Pimoule C, Graham D, Arbilla S

Plain English
This study looked at a compound called cirazoline to understand specific sites in the brain, kidneys, and pancreatic cells that recognize certain types of molecules (imidazoline sites). Researchers found that cirazoline strongly attaches to these sites without affecting common adrenaline receptors, meaning it specifically targets imidazoline recognition sites. This is important because it helps clarify how these sites work and distinguishes them from other receptors, which can aid in developing better treatments for conditions related to these sites. Who this helps: Patients with conditions related to imidazoline sites, as well as doctors looking for more targeted therapies.

PubMed

Involvement of alpha 2-adrenoceptors in metabolic and hormonal responses to a mixed meal in beagle dogs.

1995

The American journal of physiology

Guillot E, Morand R, Bouloy C, Eon MT, Angel I

Plain English
The study examined how certain receptors in the body influence the way beagle dogs respond to food in terms of blood sugar and fat levels. When a specific blocker was given before a meal, it lowered blood sugar and increased important substances like insulin and fatty acids; specifically, it reduced glucose levels significantly while boosting insulin and fatty acids. This research is important because it highlights how these receptors affect insulin and fat levels during digestion, which could help understand metabolic responses in other animals, including humans. Who this helps: This helps scientists and veterinarians who study obesity and metabolism in animals and potentially humans.

PubMed

In vitro stimulation of insulin release by SL 84.0418, a new alpha 2-adrenoceptor antagonist.

1994

European journal of pharmacology

Jonas JC, Plant TD, Angel I, Langer SZ, Henquin JC

Plain English
This study examined a new drug called SL 84.0418, which boosts insulin release in mouse cells when glucose levels are high. It found that at certain concentrations (0.1 to 100 microM), SL 84.0418 was more effective at promoting insulin release than a known medication, tolbutamide. This discovery is important because it could lead to improved treatments for people with diabetes who struggle to manage their blood sugar levels. Who this helps: Patients with diabetes.

PubMed

The imidazoline SL 84.0418 shows stereoselectivity in blocking alpha 2-adrenoceptors but not ATP-sensitive K+ channels in pancreatic B-cells.

1994

European journal of pharmacology

Jonas JC, Garcia-Barrado MJ, Angel I, Henquin JC

Plain English
Researchers studied a new drug called SL 84.0418 to see how it affects insulin release from pancreatic cells in mice. They found that while both forms of the drug helped increase insulin release when glucose levels were high and blocked the effects of certain channels, one form (deriglidole) was about 100 times more effective at blocking specific receptors that inhibit insulin release compared to the other form. This matters because it highlights a potential new treatment option for improving insulin release, which could be beneficial for managing diabetes. Who this helps: This helps patients with diabetes.

PubMed

Inhibition of insulin release induced by galanin in the dog is not exclusively mediated by activation of ATP-sensitive K+ channels.

1993

Pharmacology

Lorrain J, Angel I, Eon MT, Oblin A, Langer SZ

Plain English
This study looked at how a substance called galanin affects insulin release in dogs. Researchers found that galanin lowered insulin levels by about 50% when specific pathways in the body were blocked. This is important because it shows that galanin works in ways beyond just affecting potassium channels, which may help us understand better how insulin regulation works. Who this helps: This helps doctors and researchers who are studying insulin regulation and diabetes treatment.

PubMed

Litoxetine: a selective 5-HT uptake inhibitor with concomitant 5-HT3 receptor antagonist and antiemetic properties.

1993

European journal of pharmacology

Angel I, Schoemaker H, Prouteau M, Garreau M, Langer SZ

Plain English
Researchers studied litoxetine, a new antidepressant, to see if it could prevent nausea and vomiting, particularly when triggered by chemotherapy drugs like cisplatin. They found that litoxetine significantly reduced the number of times vomiting occurred in ferrets, with a dose of 10 mg/kg leading to a marked decrease in retching and vomiting episodes. This is important because traditional antidepressants often cause nausea, and litoxetine's ability to also block nausea-producing signals could make it safer and more comfortable for patients to use. Who this helps: This helps patients who are undergoing chemotherapy and may also need antidepressant treatment.

PubMed

In vivo pharmacological profile of SL 84.0418, a new selective, peripherally active alpha 2-adrenoceptor antagonist.

1993

European journal of pharmacology

Angel I, Grosset A, Perrault G, Schoemaker H, Langer SZ

Plain English
Researchers studied a new drug called SL 84.0418, which blocks specific receptors in the body known as alpha 2-adrenoceptors. They found that this drug effectively reduced blood sugar levels without affecting blood pressure or heart rate when tested on rats and mice. SL 84.0418 showed strong effects in blocking hyperglycemic responses, making it a significant potential treatment for managing blood sugar levels in certain conditions. Who this helps: This helps patients with conditions like diabetes who need better control of their blood sugar levels.

PubMed

The serotonin re-uptake transporter as a target for antidepressant action.

1992

Clinical neuropharmacology

Langer SZ, Graham D, Arbilla S, Schoemaker H, Angel I

PubMed

Regulation of the anorectic drug recognition site during glucoprivic feeding.

1992

Brain research bulletin

Angel I, Hauger RL, Giblin BA, Paul SM

Plain English
This study looked at how a substance called 2-deoxy-D-glucose (2-DG) affects feeding behavior and certain brain activities in rats and mice, particularly focusing on how these reactions differ between lean and obese animals. Researchers found that after giving 2-DG, lean rats and mice ate more and showed increased brain activity related to hunger signaling, whereas obese mice did not respond to 2-DG despite having higher blood sugar levels. These findings matter because they help understand why some people, especially those with obesity, might struggle to regulate their eating, which can contribute to ongoing health issues. Who this helps: This research benefits patients with obesity and healthcare professionals looking for better treatment options.

PubMed

Adrenergic and nonadrenergic cotransmitters inhibit insulin secretion during sympathetic stimulation in dogs.

1992

The American journal of physiology

Lorrain J, Angel I, Duval N, Eon MT, Oblin A +1 more

Plain English
Researchers studied how signals from the sympathetic nervous system affect insulin secretion in dogs. They found that when the sympathetic nerves were stimulated, insulin secretion decreased significantly, but this effect could be blocked by certain drugs, with glibenclamide showing a 50% reduction in the decrease. This research is important because it reveals that different types of signals, not just norepinephrine, play a role in regulating insulin release, which could have implications for diabetes treatment. Who this helps: This benefits patients with diabetes by potentially leading to new treatment strategies.

PubMed

SL 84.0418: a novel, potent and selective alpha-2 adrenoceptor antagonist: in vitro pharmacological profile.

1992

The Journal of pharmacology and experimental therapeutics

Angel I, Schoemaker H, Arbilla S, Galzin AM, Berry C +5 more

Plain English
This study looked at a new drug called SL 84.0418, which blocks a specific type of receptor in the body called the alpha-2 adrenoceptor. The researchers found that SL 84.0418 is very effective at blocking these receptors (with a value known as Ki at just 7 nanomolar) while being much less effective (with Ki at 3.3 micromolar) at blocking a different type called alpha-1 adrenoceptor, showing it is more than 1000 times more selective for the alpha-2 type. This matters because it could lead to better treatments for conditions like high blood pressure or certain types of depression, where modulating norepinephrine release is beneficial. Who this helps: Patients with cardiovascular or mood disorders.

PubMed

Pre- and postsynaptic alpha-2 adrenoceptors as target for drug discovery.

1991

Journal of neural transmission. Supplementum

Langer SZ, Angel I

Plain English
This study looked at a new drug called SL 84.0418, which blocks certain receptors in the body (alpha-2 adrenoceptors) that normally help regulate insulin and blood sugar levels. Researchers found that SL 84.0418 is much more effective at blocking these receptors compared to another drug and can significantly lower high blood sugar levels in several species, including humans. This is important because it suggests SL 84.0418 could be a new treatment option for people with type 2 diabetes. Who this helps: Patients with type 2 diabetes.

PubMed

Impairment of glucostatic, adrenergic and serotoninergic feeding parallels the lack of glucoprivic signals in the golden hamster.

1991

Brain research bulletin

Angel I, Taranger MA

Plain English
This study looked at how golden hamsters respond to low glucose levels, which typically trigger hunger. Researchers found that even when glucose levels dropped and the hamsters showed signs of high blood sugar, they did not eat more food, unlike other animals that do. This is important because it reveals that hamsters may not regulate their hunger based on glucose levels like other species, which could impact how we understand eating behavior in different animals. Who this helps: This helps researchers and veterinarians who study feeding behaviors and metabolic responses in animals.

PubMed

Frequent Co-Authors

S Z Langer S Arbilla E Guillot H Schoemaker J Goldhill A Coste M T Eon Erez Aminov D J Martin Rita Perelroizen

Physician data sourced from the NPPES NPI Registry . Publication data from PubMed . Plain-English summaries generated by AI. Not medical advice.