Korean J Anat.  2009 Dec;42(4):293-299.

Effect of Thiazolidinediones Administration on Neurochemical Composition of MPG Neurons Related to Erection in OLETF Rat

Affiliations
  • 1Department of Anatomy and Institude of Basic Medical Science, Yonsei University Wonju Collage of Medicine, Wonju, Korea. bpcho@yonsei.ac.kr
  • 2Department of Opthalmic Optics, Baekseok Culture University, Cheonan, Korea.
  • 3Department of Internal Medicine, Yonsei University Wonju Collage of Medicine, Wonju, Korea.

Abstract

The main transmitter substance mediating erection is the nitric oxide released from the vascular endothelial cells of corpus cavernosum and from the nonadrenergic, noncholinergic nerve endings. In addition, some neurotransmitters, such as acetylcholine or vasoactive intestinal polypeptide (VIP), have been reported to play an important role in mediating the erection. Thus, autonomic neuropathy may cause erectile dysfunction, and in reality, it occurs frequently in individuals with diabetes mellitus (DM), in which polyneuropathy, including both peripheral somatic sensorimotor neuropathy and autonomic neuropathy, develops usually. Thiazolidinedione (TZD) is an insulin-sensitizing agent used for the treatment of type 2 DM with insulin resistance, and has been reported to ameliorate nephropathy, decrease plasma glucose level and reduce blood pressure. However, the effect of this drug on the neuropathy related to erectile dysfunction has never been proved. In the present study, to evaluate the effect of TZDs on the neuropathy concerned with erectile dysfunction, we examined neurochemical changes of major pelvic ganglion (MPG) neurons in Otsuka Long Evans Tokushima Fatty (OLETF) rats, genetic models with non-insulin-dependent DM, after TZDs (pioglitazone and rosiglitazone) treatment. Age-matched nondiabetic Long Evans Tokushima Otsuka (LETO) rats were used as controls. Nitric oxide synthase (NOS), tyrosine hydroxylase (TH), VIP, and neuropeptide Y (NPY) contents were measured in MPG neurons of LETO, OLETF and pioglitazone- or rosiglitazone-treated OLETF rats by morphometry. Compared to the corresponding LETO group, number of TH-, NOS- and VIP-immunoreactive (ir) neurons decreased, while that of NPY-ir neurons, which modulate noradrenergic vasoconstriction of penile arteries, increased in the MPG of the OLETF group. After administration of pioglitazone- or rosiglitazone to OLETF rats for 23 weeks, these neurochemical changes were recovered to the control levels of the LETO group, although some variations were accompanied. These results suggest that TZDs treatment may be helpful for the treatment of autonomic neuropathy concerned with erectile dysfunction.

Keyword

Major pelvic ganglion; Erectile dysfunction; NOS; VIP; Diabetes mellitus; Thiazolidinedione

MeSH Terms

Acetylcholine
Animals
Arteries
Blood Pressure
Diabetes Mellitus
Endothelial Cells
Erectile Dysfunction
Ganglion Cysts
Glucose
Insulin Resistance
Male
Models, Genetic
Negotiating
Nerve Endings
Neurons
Neuropeptide Y
Neurotransmitter Agents
Nitric Oxide
Nitric Oxide Synthase
Plasma
Polyneuropathies
Rats
Rats, Inbred OLETF
Thiazolidinediones
Tyrosine 3-Monooxygenase
Vasoactive Intestinal Peptide
Vasoconstriction
Acetylcholine
Glucose
Neuropeptide Y
Neurotransmitter Agents
Nitric Oxide
Nitric Oxide Synthase
Thiazolidinediones
Tyrosine 3-Monooxygenase
Vasoactive Intestinal Peptide
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