Evidence map›Paper›PMID 39545987›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2025

Long-term effects of sub-chronic exposure to L-NAME on reproductive system of male rats.

Reshma Gaonkar, Janvi Pritmani, Mamata Datar, Dipty Singh, Nafisa Balasinor, Kumari Nishi

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Article in Naunyn-Schmiedeberg's archives of pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Reshma Gaonkar *Department of Neuroendocrinology, ICMR-National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, 400012, India.
Janvi Pritmani *Sunandan Divatia School of Science, NMIMS, Mumbai, Maharashtra, 400056, India.
Mamata DatarDepartment of Neuroendocrinology, ICMR-National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, 400012, India.
Dipty SinghDepartment of Neuroendocrinology, ICMR-National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, 400012, India.
Nafisa BalasinorDepartment of Neuroendocrinology, ICMR-National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, 400012, India.
Kumari NishiDepartment of Neuroendocrinology, ICMR-National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, 400012, India. kumarin@nirrch.res.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nω-nitro-l-arginine methyl ester (L-NAME) has been utilized as a nitric oxide synthase antagonist for many years in both basic and clinical research settings to assess its therapeutic potential. Though a number of studies have shown the effect of L-NAME on testicular function, the information regarding the reversibility of these effects upon L-NAME withdrawal is limited. In the present study, male rats (68-80 days old) divided randomly into three groups received different doses of L-NAME, i.e. 20 mg/kg bw (L20) and 10 mg/kg bw (L10) in drinking water, and drinking water only (control) through oral gavage daily for three weeks. The rats were monitored for and sacrificed after 60 days of L-NAME treatment termination. The animals had a significantly higher (p < 0.01) mean blood pressure compared to control. Aberrant histological changes were observed in the testes of L-NAME-treated rats. A significant reduction (p < 0.05) in the sperm count and an increase in abnormal sperm morphology (p < 0.05) was observed in L-NAME treated rats. Moreover, the spermatogenic cycle was found to be altered in L-NAME treated rats. No change was observed in serum estradiol levels, while serum testosterone levels were significantly increased (p < 0.05) in L10 and L20 animals. The intra-testicular testosterone was increased significantly (p < 0.01) in L20 animals. A significant decrease (p < 0.05) in superoxide dismutase activity was observed in L20 animals. The sub-chronic exposure to L-NAME resulted in higher mean arterial blood pressure and long-term testicular tissue damage, affecting sperm quality and spermatogenesis.

Indexed as

Enzyme InhibitorsNG-Nitroarginine Methyl EsterTestisAnimalsBlood PressureMaleRatsRats, WistarSpermatogenesisSpermatozoaSperm CountTestosteroneEnzyme InhibitorsNG-Nitroarginine Methyl EsterTestosteroneHypertensionL-NAMESpermatogenesisTestosteroneToxicity

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.