Sunny E. Ohia

ORCID: 0000-0002-2425-6778
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About
Contact & Profiles
Research Areas
  • Sulfur Compounds in Biology
  • Neuroscience and Neuropharmacology Research
  • Glaucoma and retinal disorders
  • Amino Acid Enzymes and Metabolism
  • Biochemical effects in animals
  • Neuroscience of respiration and sleep
  • Receptor Mechanisms and Signaling
  • Nitric Oxide and Endothelin Effects
  • Retinal Development and Disorders
  • Eicosanoids and Hypertension Pharmacology
  • Connexins and lens biology
  • Nicotinic Acetylcholine Receptors Study
  • Antioxidant Activity and Oxidative Stress
  • Retinoids in leukemia and cellular processes
  • Redox biology and oxidative stress
  • Neurotransmitter Receptor Influence on Behavior
  • Mast cells and histamine
  • Free Radicals and Antioxidants
  • Cannabis and Cannabinoid Research
  • Neurological Disorders and Treatments
  • Inflammatory mediators and NSAID effects
  • Neuropeptides and Animal Physiology
  • Advanced Glycation End Products research
  • Molecular Sensors and Ion Detection
  • Traditional and Medicinal Uses of Annonaceae

Texas Southern University
2016-2025

Creighton University
1996-2019

University of Houston
2003-2008

CHI Health Creighton University Medical Center - Bergan Mercy
2004

Langston University
2003

University of Louisville
1990-1993

Smith-Kettlewell Eye Research Institute
1990-1993

Both hydrogen sulfide and endocannabinoids can protect the neural retina from toxic insults under in vitro vivo conditions. Purpose: The aim of present study was two-fold: (a) to examine neuroprotective action cannabinoids [methanandamide 2-arachidonyl glycerol (2-AG)] against peroxide (H2O2)-induced oxidative damage isolated bovine (b) evaluate role endogenously biosynthesized (H2S) inhibitory actions on stress retina. Methods: Isolated retinas cows were exposed using H2O2 (100 µM) for 10...

10.3390/ph18010117 article EN cc-by Pharmaceuticals 2025-01-17

In this study, we investigated the effect of a slow-releasing hydrogen sulfide (H2S) donor, GYY 4137, on intraocular pressure (IOP) in normotensive rabbits. Furthermore, compared IOP-lowering action 4137 with those elicited by other H2S-producing compounds, l-cysteine and ACS67 (a hybrid compound latanoprost an H2S-releasing moiety).IOP was measured New Zealand male albino rabbits using pneumatonometer (model 30 classic; Reichert Ophthalmic Instruments, Depew, NY). At 0 h, 50 μL test...

10.1089/jop.2015.0144 article EN Journal of Ocular Pharmacology and Therapeutics 2016-04-19

Both naturally occurring and synthetic prostaglandins (PGs) caused concentration-dependent inhibition of electrically evoked [3H]norepinephrine (NE) overflow from the isolated, superfused rabbit iris-ciliary body without affecting basal tritium efflux. The rank order potencies agonists was: sulprostone greater than 16, 16-dimethyl-PGE2 PGE2 11-deoxy-PGE1 iloprost (stable PGl2 analog) PGF2 alpha or equal to PGD2. However, Tx-mimetic, U-46619, was effect on transmitter release at...

10.1016/s0022-3565(25)12704-3 article EN Journal of Pharmacology and Experimental Therapeutics 1990-10-01

Prostaglandins (PGs) of the E series have been shown to modulate sympathetic neurotransmitter release in a variety peripheral tissues and organs, including eye. In this study, we evaluated inhibitory effects naturally-occurring synthetic PGs on field stimulation-evoked 3H-norepinephrine (3H-NE) from isolated, superfused segments human iris-ciliary body. Field-stimulated 3H-NE secretion was calcium-dependent, blocked by selective inhibitors voltage-sensitive calcium sodium channels,...

10.3109/02713689109020333 article EN Current Eye Research 1991-01-01
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