Significant Cellular Changes in Rat's Vital Organs After Only 4 Weeks on Benzos

 

Jill Scott - Hate on Me

 

 

If I could give you the world on a silver platter

Would it even matter, you'd still be mad at me

If I could find in all this a dozen roses

Which I would give to you, you'd still be miserable

Here reality I'm gon' be who I be and I don't feel no faults

For all the lies that you bought

You can try as you may, break me down but I say

That it ain't up to you, gone and do what you do

Hate on me, hater, now or later

'Cause I'm gonna do me, you'll be mad, baby

Go 'head and hate on me, hater, I'm not afraid of

What I got I paid for, you can hate on me

Ooh, if I gave you peaches outta my own garden

And I made you a peach pie, would you slap me high

Wonder if I gave you diamonds out of my own womb

Would you feel the love in that or ask why not the moon

If I gave you sanity for the whole of humanity

Had all the solutions for the pain and pollution

No matter where I live, despite the things I give

You'll always be this way, so go 'head and

Hate on me, hater, now or later

'Cause I'm gonna do me, you'll be mad, baby

Go 'head and hate on me, hater, I'm not afraid of

What I got I paid for, you can hate on me (repeat)

You cannot hate on me 'cause my mind is free

Feel my destiny, so shall it be

You cannot hate on me 'cause my mind is free

Feel my destiny, so shall it be

Hate on me, hater, now or later

'Cause I'm gonna do me, you'll be mad, baby

Go 'head and hate on me, hater, I'm not afraid of

What I got I paid for, you can hate on me (repeat)

You cannot hate on me 'cause my mind is free

Feel my destiny, so shall it be

You cannot hate on me 'cause my mind is free

Feel my destiny, so shall it be

Hate on me, hater, now or later

'Cause I'm gonna do me, you'll be made, baby

Go 'head and hate on me, hater, I'm not afraid of

What I got I paid for, you can hate on me

 

 

 

We (I) will pick back up here by Monday, likely, and continue.

.

First thing I thought was..... poor rats are gonna have to go through withdrawal.   

I said poor rats and mice too.  It was sad to read those studies.  The mice were scared and wouldn't explore when they took them off the benzo's.  Brain-damaged.

This is no fun to do, I don’t want to point people over here anymore or try to convince anyone— it takes a toll.

 

Thanks you two, I’m done. Really.

Just thought is drag this back in for discussion... or not. Merry Christmas!

Differential effects of alprazolam and clonazepam on the immune system and blood vessels of non-stressed and stressed adult male albino rats

 

Ghada E. Elmesallamy, Marwa A. Abass, [...], and Amal H. Atta

 

Additional article information

 

Abstract

 

Benzodiazepines belongs to one of the most commonly used anxiolytic and anticonvulsant drugs in the world. Full description of toxic effects on different organs is lacking for nearly all the current benzodiazepines. The aim of the current work was to study the immunologic and vascular changes induced by sub-chronic administration of alprazolam and clonazepam in non-stressed and stressed adult male albino rats. Forty-two adult male albino rats were divided into 6 groups (I): (Ia) Negative control rats, (Ib): Positive control rats received distilled water, (II): Stressed rats, (III): Non-stressed rats received daily oral dose of clonazepam (0.5 mg/kg), (IV): Stressed rats received daily oral dose of clonazepam (0.5 mg/kg), (V): Non-stressed rats received daily oral dose of alprazolam (0.3 mg/kg). (VI): Stressed rats received daily oral dose of alprazolam (0.3 mg/kg). At the end of the 4th week, total leukocyte count (WBCs) and differential count were determined, anti-sheep RBC antibody (Anti-SRBC) titer and interleukin-2 (IL-2) level were assessed, thymus glands, lymph nodes, spleens and abdominal aortae were submitted to histopathological examination. Alprazolam was found to induce a significant increase in neutrophil count and a significant decrease in lymphocytes, anti-SRBC titer and IL-2 level with severe depletion of the splenic, thymal and nodal lymphocytes, accompanied by congestion and eosinophilic vasculitis of all organs tested in comparison to clonazepam treated rats. Stress enhanced the toxic effects. It was concluded that the immune system and blood vessels can be adversely affected to a greater extent by short-term chronic administration of alprazolam than by clonazepam, and these toxic effects are aggravated by stress.

 

Keywords: alprazolam, clonazepam, stress, SRBC, IL-2

Introduction

 

Recent studies have found that stress plays a role in the etiology of many diseases. Stress is generally considered to be immunosuppressive and to increase susceptibility to infections and cancer. Paradoxically, it also exacerbates inflammatory and autoimmune diseases. Although it is well established that stress alters the release of various hormones and neurotransmitters, the mechanisms by which stress affects immune responses remain elusive (Viswanathan et al., 2005; Salak-Johnson & McGlone, 2007).

 

Benzodiazepines (BZD) are among the most commonly used groups of anxiolytic drugs in the world. They are indicated for treatment of generalized anxiety disorders, treatment of panic disorders with or without agoraphobia, sedation, light anesthesia and anterograde amnesia of perioperative events, control of seizures, and skeletal muscle relaxation (Iqbal et al., 2002).

 

Clonazepam, a benzodiazepine derivative, is used for the treatment of epilepsy, psychiatric and neurologic disorders, including panic disorders. It has also been utilized in alleviating movement disorders and restless leg syndrome in patients with end-stage renal disease (Brouns & De Deyn 2004; Morishita, 2009).

 

Alprazolam is one of the most commonly prescribed short-acting benzodiazepines in the childbearing period. It has replaced diazepam in drug prescription for treatment of anxiety disorders. This shift in the pattern of drug prescription was justified by the low likelihood of its accumulation (compared with diazepam) and by the sedative effects of multiple doses (Pinna et al., 1997).

 

All benzodiazepines, including clonazepam and alprazolam, act by enhancing γ-aminobutyric acid GABA-ergic neurotransmission through the binding on specific BZD recognition sites, within the GABA (A) receptor-ion channel complex. However, it has been found that BZD also act on peripheral benzodiazepine receptor sites (PBR) or translocator protein 18kDa (TSPO) (Gavish et al., 1999). Evidence for a direct immunomodulatory action for BZD emerged from recent studies demonstrating the presence of TSPO on immune/inflammatory cells (De Lima et al., 2010).

 

The production of antigen-specific antibodies represents a major defense mechanism of humoral immune responses. Data suggest that the primary antibody response to anti-sheep RBC antibody (Anti-SRBC) may be one of the most sensitive endpoints available to assess chemically induced alterations of the immune system. This endpoint has become the cornerstone of several recently established guidelines for assessing the potential immunotoxicity of xenobiotics (Ladics, 2007).

 

Interleukin 2 (IL-2) is secreted primarily by activated T-lymphocytes and natural killer (NK) cells. It is necessary for regulatory T cell maturation in the thymus and may also sensitize antigen-activated T cells to apoptosis. The importance of IL-2 in supporting the immune response makes this cytokine and its receptor a prime target for both activation and suppression. Additionally, its inhibition is critical for immunosuppression (Malek, 2003; Leo & Hsieh, 2008).

 

On reviewing the available literature from a toxicological point of view it was noticed that there was little information regarding the influence of clonazepam and alprazolam on different body tissues and cells, including the immune and vascular system. Most of the studies were focused on their alteration of the immune function rather than the structure. Therefore it was thought to be of particular interest to study the toxic effects of these commonly used drugs on these tissues at their maximum therapeutic doses.

 

The aim of the current work was to study the differential immunologic and vascular changes induced by sub-chronic administration of clonazepam and alprazolam in non stressed and stressed adult male albino rats.

 

Material and methods

 

Drugs

 

Clonazepam was obtained from Roche, F. Hoffmann-La Roche LTd, Basel, Switzerland in the form of a sterile oral solution containing 2.5 mg/ml, supplied with its dropper (1 drop contains 0.1 mg clonazepam). On administration, each 0.5 mg of the drug was diluted with 5 ml of distilled water.

 

Alprazolam in the form of white crystalline powder, was obtained from Amoun Pharmaceutical Industries Co., freshly prepared for oral gavage by dissolving it in distilled water (each 0.3 mg dissolved in 5 ml of distilled water).

 

Kits

 

Mouse Interleukin-2 (IL-2) ELISA kit of Bioscience, Inc, Catalog Number: 88-7024 was used as an enzyme-linked immunosorbent assay for quantitative measurement of IL-2 in serum.

 

Sheep RBCs

 

Sheep RBCs were obtained from the laboratory of Zoology Department, Faculty of Veterinary Medicine, Zagazig University.

 

Experimental design

 

Forty-two adult male albino rats of 200 g average weight were brought from the Animal House, Faculty of Medicine, Zagazig University, divided into 6 groups and caged under standardized environmental conditions.

 

Group I: Twelve rats were equally subdivided into (Ia): Negative control non-stressed rats, received only the regular diet and tap water to determine the normal values of the performed tests. (Ib): Positive control non-stressed rats, gavaged daily with 1 ml of distilled water.

Group II: Six stressed rats, were submitted to daily restraint stress at room temperature.

Group III: Six non stressed rats were given daily oral dose of Clonazepam (0.5 mg/kg) (Paget & Barnes, 1964) for 4 weeks.

Group IV: Six stressed rats were given daily oral dose of Clonazepam (0.5 mg/kg) for 4 weeks.

Group V: Six non-stressed rats were given daily oral dose of Alprazolam (0.3 mg/kg) (Paget & Barnes, 1964) for 4 weeks.

Group VI: Six stressed rats were given daily oral dose of Alprazolam (0.3 mg/kg) for 4 weeks.

Both drugs were assessed in their maximum therapeutic dose used for treatment of generalized anxiety disorders.

 

At the end of the study, the rats were anesthetized with ether and 5 ml blood was collected from their retro-orbital plexus. Total leukocyte count and differential count were determined and immunological studies were performed by measuring the anti-sheep RBC hemagglutination (anti-SRBC) titer and the level of serum Interleukin-2 (IL-2). The rats were then sacrificed, the thymus glands, lymph nodes, spleens and abdominal aortae were dissected and submitted to histopathological examination.

 

Restraint stress procedure

 

It was done by the procedure described by Glavin et al. (1994). Stress was applied by placing the animals (without squeezing or compression) in well-ventilated wire mesh restrainers for a single daily session of 2.5 h beginning at 9:00 a.m. This procedure mimics stress that is largely psychological in nature.

 

WBCs count and differential count

 

Total leukocyte count was determined by following the method described by Chanarin et al. (1973), using Coulter T660 hematology analyzer, Beckman Coulter, Inc., USA. Two ml of blood were collected in tubes containing 20 µl EDTA solution and differential count was done on Leishman stained peripheral blood smear.

 

Humoral immune response

 

It was assayed by the Sheep RBC Antibody Titer (SRBC): In this test 1.5 ml of blood was collected, the serum was separated and analyzed for hemagglutination titer according to the method described by Ladics et al. (2000). Two-fold dilutions (0.025 mg) of sera were made in the microtiter plates with saline. To each well 0.025 ml of 1% (v/v/) SRBC was added. The plates were incubated at 37 °C for 1 h and then observed for hemagglutination. The highest dilution giving hemagglutination was taken as the antibody titer. The antibody titers were expressed in a graded manner, the minimum dilution (1/2) being ranked as 1. The mean ranks of different groups were compared for statistical analysis.

 

Cell-mediated immune response

 

It was assayed through determination of the cytokine Interleukin-2 (IL-2): 1.5 ml blood samples were left to clott and were then centrifuged at 3 000 rpm for 10 minutes. Serum samples were separated and kept frozen at −20 °C for determination of interleukin-2 (IL-2) by Enzyme Linked-Immuno-Sorbent Assay (ELISA) according to the method described by Hollander et al. (1998). The data analysis program automatically determined the concentrations of IL-2 in the samples by comparing the absorbency of the samples to the standard curve which demonstrated an inverse relationship between Optical Density (O.D.) and the cytokine concentration. IL-2 concentration was represented as pg/ml.

 

Histopathological examination

 

Paraffin blocks and sections of thymus glands, lymph nodes, spleens and abdominal aortae were prepared, stained with hematoxylin and eosin and subjected to routine histological examination by the method described by Bancroft & Stevens (1996).

 

Statistical analysis

 

SPSS Software program was used. Mean values (M)±SD were calculated. t-test and F test were performed. P value of less than 0.05 was considered to be significant.

 

Results

 

At the end of the 4th week of the current study, comparison between negative control rats (Group Ia) and positive control rats (Group Ib) showed a non-significant difference in all parameters tested (p>0.05) (Table 1)

 

Table 1

Table 1

Immunologic parameters in the different study groups after 4 weeks (Anova test).

Stressed non-treated rats (Group II) showed a significant increase (p<0.05) in the mean values of neutrophils as compared to control group. However, they showed a non-significant change regarding the mean values of WBCs, lymphocytes, eosinophils and monocytes, when compared with those of the control group (p>0.05). They also exhibited a significant decrease (p<0.001) in the mean values of anti-SRBC titer and a non-significant decrease (p>0.05) in the mean values of IL-2 compared to the control group, as shown in Table 1.

 

Histopathological examination of the same group (Group II) showed minimal changes in the spleens and lymph nodes in the form of slight subcapsular edema, as seen in Figures (​(2-a,2-a, ​-a,2-b),2-b), when compared to the normal architecture of the control group (Figures 1-a, ​-a,1-b).1-b). The thymuses showed a mild subcapsular edema, while the aortae displayed eosinophilic vasculitis (Figures 2-c, ​-c,2-d)2-d) as compared to the control group (Figures 1-c, ​-c,11-d).

 

Figure 1

Figure 1

Control rat (group I): a) Spleen section showing normal structure (H&E, × 200), b) Lymph node section showing normal structure (H&E, × 200), c) Thymus section showing normal structure (H&E, × 400), d) Large ...

Figure 2

Figure 2

Stressed non-treated rat (group II): a) Spleen section showing normal white pulp and proliferation of reticular cells (H&E, × 200), b) Lymph node section showing normal lymphoid follicles and mild subcapsular edema (H&E, × ...

Clonazepam-treated non-stressed rats (Group III) showed a non-significant change (p>0.05) in the mean values of WBCs, lymphocytes, neutrophils, eosinophils and monocytes when compared with those of the control group (Group I). They also exhibited a significant decrease (p<0.001) in the mean values of anti-SRBC titer and a non significant decrease (p>0.05) in the mean value of IL-2 level as compared to the control group. (Table 1).

 

Comparison between the clonazepam-treated non stressed rats (Group III) and the stressed non-treated rats (Group II) showed a non-significant change (p>0.05) in the mean values of all immunologic parameters tested except neutrophils. A significant increase (p<0.05) in the mean values of neutrophils was observed when compared with Group II, as shown in Table 2.

 

Table 2

Table 2

Comparison of the mean values for each parameter assessed in the different study groups (LSD test).

The observed changes in the tested organs of the same group (Group III) were in the form of congested red pulp of the spleens with normal white pulp and slight depletion of the lymphoid follicles in the lymph node specimens (Figures 3-a, ​-a,3-b).3-b). Thymus glands showed subcapsular lymphoid follicles (Figure 3-c). Examination of the aortic tissues revealed multiple plaques protruding inside the arterial lumen. These plaques were composed of smooth muscles and deposition of some foam cells (Figure 3-d).

 

Figure 3

Figure 3

Clonazepam-treated unstressed rat (group III): a) Spleen section showing normal white pulp and congested red pulp (H&E, × 200), b) Lymph node section showing mild edema among slightly depleted lymphoid follicles (H&E, × ...

Clonazepam-treated stressed rats (Group IV) revealed a significant increase (p<0.05) in the mean values of neutrophils. However, the mean values of WBCs, lymphocytes, eosinophils, and monocytes showed a non-significant change (p>0.05) when compared with control rats (Group I). There was also a significant decrease (p<0.001) in the mean values of anti-SRBC titer and IL-2 level as compared to the control group (Tables 1 and ​and22)

 

Moreover, in stressed rats (Group IV) clonazepam treatment was found to induce hyaline degeneration of the wall of splenic arterioles with perivascular edema (Figure 4-a). Lymph nodes examination showed mild depletion of lymphocytes from subcapsular lymphoid follicles (Figure 4-b). The thymuses exhibited mild depletion of the cortical lymphoid follicles and medullary congestion (Figure 4-c). However, the media and intima of the arterial wall presented no changes (Figure 4-d).

 

Figure 4

Figure 4

Clonazepam-treated stressed rat (group IV): a) Spleen section showing hyaline degeneration of the wall of splenic arteriole and perivascular edema (H&E, × 400), b) Lymph node section showing mild depletion of lymphocytes from subcapsular ...

Alprazolam-treated non-stressed rats (Group V) showed a non-significant change (p>0.05) in the mean values of WBCs, lymphocytes, neutrophils, eosinophils and monocytes when compared with control rats (Group I). The mean values of anti-SRBC titer and IL-2 level presented a significant decrease (p<0.001) as compared to the control group (Tables 1 and ​and22)

 

Spleen sections of the same group (Group V) showed depletion of the marginal lymphocytes in the white pulp (Figure 5-a) and lymph nodes had a slight depletion of the lymphoid follicles, as shown in Figure 5-b. Thymus glands also had a mild depletion of lymphocytes from the lymphoid follicles and mild interstitial edema (Figure 5-c). On examination of aortic sections, edematous walls, composed of degenerated muscles with endotheliosis were observed (Figure 5-d).

 

Figure 5

Figure 5

Alprazolam-treated unstressed rat (group V): a) Spleen section showing depletion of the marginal lymphocytes in the white pulp (H&E, × 400), b) Lymph node section showing mild depletion of lymphocytes from subcapsular lymphoid follicles ...

Comparison between alprazolam-treated stressed rats (Group VI) and control rats (Group I), showed a significant decrease (p<0.05) in the mean values of lymphocytes and a significant increase (p<0.05) in those of neutrophils. In contrast, a non-significant change (p>0.05) was detected in the mean values of WBCs, eosinophils and monocytes. The mean values of anti-SRBC and IL-2 presented a significant decrease (p<0.001) when compared with those of control rats. (Tables 1 and ​and22).

 

On comparing the immunologic findings of alprazolam-treated stressed rats (Group VI) with those of the stressed non-treated rats (Group II), a significant decrease (p<0.001) was seen in the mean values of anti-SRBC titer and IL-2 level (Table 2)

 

Histopathological findings of the same group (Group VI) supported the previous results. Severe depletion of the white pulp lymphocytes and extensive hemorrhages in the red pulp with hemosiderosis and degenerated megakaryocytes were noticed on examination of spleen sections. Moreover, edema and histocyte infiltrations were also observed in the red pulp of the spleens (Figures 6-a, ​-a,6-b).6-b). Focal replacement of subcapsular follicles of the lymph nodes by reticular cells and macrophages was also detected (Figure 6-c). Furthermore, thymus glands showed marked edema and congestion with few erythrocyte and leukocyte infiltrations (Figure 6-d). Eosinophilic vasculitis was evident on examination of aortic sections with thick tunica media. Eosinophils and round cell infiltrations in the tunica adventitia were also noticed, as shown in Figure 6-e.

 

Figure 6

Figure 6

Alprazolam-treated stressed rat (group VI): a) Spleen section showing severe depletion of lymphocytes from the white pulp and extensive hemorrhages in the red pulp (H&E, × 400), b) Spleen section showing hemosiderosis, degenerated megakaryocytes ...

When comparing clonazepam-treated non-stressed rats (Group III) and alprazolam-treated non-stressed rats (Group V), a non-significant difference (p>0.05) was found in most of the parameters tested. An exception was the anti-SRBC titer, as alprazolam induced a significant decrease (p<0.05) in its mean values when compared to those of clonazepam-treated non-stressed rats. Comparison between clonazepam-treated stressed rats (Group IV) and alprazolam-treated stressed rats (Group VI), showed that alprazolam induced a significant decrease (p<0.05) in the mean values of IL-2 level compared with those induced by clonazepam (Table 2)

 

Finally, on observing the differential toxic effects of clonazepam treatment in non-stressed rats (Group III) and in stressed rats (Group IV), a significant decrease (p<0.05) in the mean values of anti-SRBC titer and IL-2 level was found in the clonazepam-treated stressed rats. Regarding the differential toxic effects of alprazolam treatment in non-stressed rats (Group V) and stressed rats (Group VI), it was found that alprazolam induced a significant increase (p<0.05) in the mean values of neutrophils and a significant decrease in the mean values of anti-SRBC titer and IL-2 level in stressed rats (Group VI) compared to non-stressed rats (Group V), as shown in Table 2.

 

Discussion

 

Benzodiazepines (BZPs) are widely used drugs as tranquilizers, anticonvulsants and in various other indications as light anesthesia and skeletal muscle relaxation. However, not all benzodiazepines have been tested for their immunotoxic effects (Huemer et al., 2010).

 

In the current study two commonly prescribed BZPs (clonazepam and alprazolam) were selected to study their immunologic and vascular toxic potential. Both anti-SRBC titer and IL-2 level were used to assess the humoral and cell-mediated immune functions.

 

IL-2 is necessary for the maturation of thymus lymphocytes, facilitation of immunoglobulin production made by B cells, and the differentiation and proliferation of natural killer cells (Malek, 2003; Waldmann, 2006).

 

Moreover, it was observed that small numbers of sheep red blood cells (SRBC) markedly augmented the proliferation of T lymphocytes activated by antigens or mitogens. This effect occurred with as few as one SRBC per T lymphocyte and with intact or osmotically lysed red cells. It was also accompanied by increase in interleukin-2 (Guo & White, 2010).

 

After 4 weeks of clonazepam and alprazolam administration, more pronounced immunologic and vascular toxic effects were demonstrated in stressed than in non-stressed adult male albino rats. These toxic changes were significantly expressed in the immunologic parameters as neutrophils, lymphocytes, anti-SRBC, and IL-2 (especially in alprazolam-treated stressed rats), supported by the histopathological findings as depletion of lymphocytes from the spleens, lymph nodes and thymuses, congestion, edema, hemosiderosis, inflammatory cells infiltration, large vessels eosinophilic infiltration, vasculitis, plaques and degeneration.

 

Our results are in accordance with those of Massoco and Palermo-Neto (2003) and Huemer et al. (2010) who stated that many benzodiazepines induced prolonged impairment of cellular immune functions in experimental animals after chronic low-dosage administration.

 

It has been substantiated that stressful stimuli in man as well as in animals lead to suppression of the humoral and cellular components of the immune system. The central nervous system is known to be involved in the regulation of stress-induced immune responsiveness (Yin et al., 2000).

 

The results of the present study also showed that restraint stress produced an inhibition of SRBC antibody, that was worsened by the administration of either clonazepzm or alprazolam with inhibition of IL-2. Kalashnikov et al. (2002) found that exposure to low doses of BDZ resulted in long-lasting reduction of TNF-alpha, IL-1, IL-6, IL-2 and interferon-gamma.

 

In 1991, Chang et al. found that alprazolam induced severe inhibitory effects on the proliferative responses of both B- and T-cells. It also reduced the production of IL-2 by splenic T-cells, IL-1 and tumor necrosis factor (TNF) by peritoneal macrophages. Moreover, long-lasting depression of lymphocytic proliferation has been described in offspring of rats exposed to either diazepam or clonazepam during pregnancy (Schlumpf et al., 1991).

 

Regarding the toxic effects on differential WBC counts, Bautista-Quach et al. (2010) reported a case of pancytopenia following oral administration of 0.25 mg clonazepam twice a day for approximately two weeks.

 

Lymphocytic depletion, similar to that observed in the current study, was noticed in both red and white pulp of the spleen in rats treated with diazepam (0.1 mg) daily for 4 weeks (Moris, 1991). Moreover, the observed hemosideriosis in spleens of alprazolam-treated stressed rats may be attributed to increased erythrophagia (Pacheco and Santos, 2002). In this context, it was found that diazepam accelerateed RBCs destruction via inhibition of Ca+2 ATPase on RBCs membrane (Seckin et al., 2007).

 

Several reports identified BZP peripheral type binding sites (PBR) in endocrine steroidogenic tissues, organs and cells of the immune system, such as macrophages and lymphocytes. Thus, the PBR may be a possible primary target for the immunotoxic effects of BDZ (Righi et al., 1999).

 

In the current study, immune and vascular toxic effects might be related to cortisol production. West et al., (2001) stated that stimulation of PBR in steroidogenic tissues such as the adrenals increaseed glucocorticoid production. Glucocorticoid hormones are known for their potent immunosuppressive and anti-inflammatory properties.

 

Corticosteroids have been shown to promote the immune response during acute stress and to inhibit the immune response during chronic stress (Dhabhar & McEwen, 1997). On the other hand, restraint stress was found to induce corticosterone secretion (Li et al., 2000).

 

Elevated endogenous corticosteroid levels were linked to reduced spleen cellularity and B cell function in mice (Shi et al., 2003). Moreover, they produced neutrophilic leukocytosis, lymphopenia and reduced anti-SRBC titer and IL-2 level, a picture similar to that detected in the present study (Anderson et al., 1999; Obmiñska-Mrukowicz & Szczypka, 2004).

 

Alprazolam was tested previously for its effects on corticosteroid production. Chronic administration of alprazolam for 29 days to hamster rats resulted in increased cortisol and total glucocorticoid levels. It was concluded that alprazolam had a stimulative effect on cortisol production (Arvat et al., 1999).

 

On the other hand, clonazepam was shown to counteract the effect of stress on cortisol level (Chevassus et al., 2004).

 

In this context, the cytokine system emerges as a good candidate. Indeed, the production and release of cytokines are known to mediate both inflammatory and immune responses (Wiegers & Reul, 1998) and not only cortisol (Almawi et al., 1996). Schlumpf et al., (1994) reported that PBR stimulation of macrophage and lymphocyte membranes changed the cytokine network.

 

Interestingly, the action of the PBR ligands seems to be connected with blockage of voltage-dependant Ca+2 channels (Ostuni et al., 2004). Calcium release appears to be essential for T cell activation, cytokine synthesis, and proliferation. Both increases and decreases in intracellular Ca2+ have been linked to apoptosis (Lepple-Wienhues et al., 1999; Mason, 1999).

 

Clonazepam was found to have a strong binding capacity to peripheral benzodiazepine receptors in rat aortic smooth muscles compared to other benzodiazepines. These binding sites were concentrated in the mitochondria (Cox et al., 1991).

 

Peripheral benzodiazepine receptors bind with high affinity to cholesterol and transport it across the mitochondrial membrane (Papadopoulos et al., 1997). This may explain the appearance of foam cells and degeneration of smooth muscle observed in the aortae of clonazepam treated rats.

 

Tanimoto et al. (1999) found that stimulation of the thymus PBR induced apoptosis in thymocytes. This action was accentuated by dexamethasone administration.

 

Ekonomopoulou et al., (2010) reported that alprazolam, diazepam, and lorazepam exhibited cytogenetic activity in normal human lymphocyte cultures. A possible mutagenic action could explain their immunotoxic effects (Giri & Banerjee, 1996).

 

Furthermore, an in vitro study carried out by Saha et al. (2009) concluded that alprazolam strongly interacted with DNA, resulting in conformational changes in the DNA. Similarly, Iakovidou-Kritsi et al., (2009) found that alprazolam induced genotoxicity and cytotoxicity in human lymphocyte cell culture at doses equivalent to oral doses, with a significant increase of Sister Chromatid Exchanges on peripheral human lymphocytes in vivo.

 

It seems relevant to point out that alprazolam has a triazolo- ring, and a – CH3 – group that could interact with DNA as an alkylating agent (Brambilla et al., 2007).

 

In contrast to the present results, Freire-Garabal et al., (1991) found that chronic administration of alprazolam for one month alleviated stress-induced suppression of thymus and spleen cellularity in mice after laparotomy. Covelli et al., (1998) also reported that alprazolam behaved as an immunoenhancer (enhancing the function.of immune cells).

 

Clonazepam and alprazolam appeared to modulate immune responsiveness in both non-stressed and stressed animals, albeit in a different manner, and these effects were mediated via alteration of the structure of organs of the immune system (histopathological lesions).

 

It was concluded that the immune system and blood vessels can be adversely affected by sub-chronic administration of alprazolam to a greater extent than by clonazepam, and these toxic effects are aggravated by stress. Further, the results of the present study raise concern regarding the safety of benzodiazepine administration over long periods.

 

Acknowledgements

 

Great thanks and gratefulness to Zoology Department, Faculty of Veterinary Medicine, Zagazig University for supplying sheep RBCs and information required for Anti-SRBC titer.

 

Article information

 

Interdiscip Toxicol. 2011 Sep; 4(3): 132–143.

Published online 2011 Sep. doi: 10.2478/v10102-011-0021-y

PMCID: PMC3203915

PMID: 22058654

Ghada E. Elmesallamy,1 Marwa A. Abass,1 Nahla A.G. Ahmed Refat,2 and Amal H. Atta3

1Department of Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Zagazig University, Egypt

2Department of Pathology, Faculty of Veterinary Medicine, Zagazig University, Egypt

3Department of Microbiology, Faculty of Medicine, Zagazig University, Egypt

Correspondence address: Assist. Prof. Ghada Elsaid Ahmed Elmesallamy, MD. Assistant Professor of Clinical Toxicology, Department of Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Zagazig University, Egypt. TEL.: +20552302809, E-MAIL: moc.liamtoh@0142annag

Received 2011 Feb 20; Revised 2011 Jul 1; Accepted 2011 Jul 21.

Copyright © 2011 Slovak Toxicology Society SETOX

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

This article has been cited by other articles in PMC.

Articles from Interdisciplinary Toxicology are provided here courtesy of Slovak Toxicology Society SETOX & Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences

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That study was quite upsetting to read.  Benzo's also changed the DNA.

 

Yes, there's no question that the use of Benzo's triggers epigenetic changes (changes in gene expression.)  Among other things, this explains protracted withdrawal.  It takes a long time to reverse these effects...to turn off newly activated genes and turn old ones back on.

 

For a deep dive, google gene transcription factors, gene tagging and epigenetics.